-
1
-
-
0037205048
-
The phosphoinositide 3-kinase pathway
-
Cantley LC. The phosphoinositide 3-kinase pathway. Science 2002; 296: 1655-7.
-
(2002)
Science
, vol.296
, pp. 1655-1657
-
-
Cantley, L.C.1
-
2
-
-
13844312400
-
Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex
-
Sarbassov DD, Guertin DA, Ali SM, Sabatini DM. Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex. Science 2005; 307: 1098-101.
-
(2005)
Science
, vol.307
, pp. 1098-1101
-
-
Sarbassov, D.D.1
Guertin, D.A.2
Ali, S.M.3
Sabatini, D.M.4
-
5
-
-
67651148274
-
Evidence that inositol polyphosphate 4-phosphatase type II is a tumor suppressor that inhibits PI3K signaling
-
Gewinner C, Wang ZC, Richardson A, et al. Evidence that inositol polyphosphate 4-phosphatase type II is a tumor suppressor that inhibits PI3K signaling. Cancer Cell 2009; 16: 115-25.
-
(2009)
Cancer Cell
, vol.16
, pp. 115-125
-
-
Gewinner, C.1
Wang, Z.C.2
Richardson, A.3
-
6
-
-
20144387695
-
PIK3CA mutations correlate with hormone receptors, node metastasis, and ERBB2, and are mutually exclusive with PTEN loss in human breast carcinoma
-
Saal LH, Holm K, Maurer M, et al. PIK3CA mutations correlate with hormone receptors, node metastasis, and ERBB2, and are mutually exclusive with PTEN loss in human breast carcinoma. Cancer Res 2005; 65: 2554-9.
-
(2005)
Cancer Res
, vol.65
, pp. 2554-2559
-
-
Saal, L.H.1
Holm, K.2
Maurer, M.3
-
7
-
-
51049118140
-
An integrative genomic and proteomic analysis of PIK3CA, PTEN, and AKT mutations in breast cancer
-
Stemke-Hale K, Gonzalez-Angulo AM, Lluch A, et al. An integrative genomic and proteomic analysis of PIK3CA, PTEN, and AKT mutations in breast cancer. Cancer Res 2008; 68: 6084-91.
-
(2008)
Cancer Res
, vol.68
, pp. 6084-6091
-
-
Stemke-Hale, K.1
Gonzalez-Angulo, A.M.2
Lluch, A.3
-
8
-
-
80755127903
-
Mutations in the phosphatidylinositol 3-kinase pathway: Role in tumor progression and therapeutic implications in breast cancer
-
Miller TW, Rexer BN, Garrett JT, Arteaga CL. Mutations in the phosphatidylinositol 3-kinase pathway: role in tumor progression and therapeutic implications in breast cancer. Breast Cancer Res 2011; 13: 224.
-
(2011)
Breast Cancer Res
, vol.13
, pp. 224
-
-
Miller, T.W.1
Rexer, B.N.2
Garrett, J.T.3
Arteaga, C.L.4
-
9
-
-
74049107249
-
PI3K pathway activation in breast cancer is associated with the basal-like phenotype and cancer-specific mortality
-
Lopez-Knowles E, O'Toole SA, McNeil CM, et al. PI3K pathway activation in breast cancer is associated with the basal-like phenotype and cancer-specific mortality. Int J Cancer 2010; 126: 1121-31.
-
(2010)
Int J Cancer
, vol.126
, pp. 1121-1131
-
-
Lopez-Knowles, E.1
O'Toole, S.A.2
McNeil, C.M.3
-
10
-
-
79957917078
-
PI3K inhibition results in enhanced HER signaling and acquired ERK dependency in HER2-overexpressing breast cancer
-
Serra V, Scaltriti M, Prudkin L, et al. PI3K inhibition results in enhanced HER signaling and acquired ERK dependency in HER2-overexpressing breast cancer. Oncogene 2011; 30: 2547-57.
-
(2011)
Oncogene
, vol.30
, pp. 2547-2557
-
-
Serra, V.1
Scaltriti, M.2
Prudkin, L.3
-
11
-
-
78651458656
-
AKT inhibition relieves feedback suppression of receptor tyrosine kinase expression and activity
-
Chandarlapaty S, Sawai A, Scaltriti M, et al. AKT inhibition relieves feedback suppression of receptor tyrosine kinase expression and activity. Cancer Cell 2011; 19: 58-71.
-
(2011)
Cancer Cell
, vol.19
, pp. 58-71
-
-
Chandarlapaty, S.1
Sawai, A.2
Scaltriti, M.3
-
12
-
-
32944457518
-
mTOR inhibition induces upstream receptor tyrosine kinase signaling and activates Akt
-
O'Reilly KE, Rojo F, She QB, et al. mTOR inhibition induces upstream receptor tyrosine kinase signaling and activates Akt. Cancer Res 2006; 66: 1500-8.
-
(2006)
Cancer Res
, vol.66
, pp. 1500-1508
-
-
O'Reilly, K.E.1
Rojo, F.2
She, Q.B.3
-
13
-
-
80655126355
-
mTOR kinase inhibition causes feedback-dependent biphasic regulation of AKT signaling
-
Rodrik-Outmezguine VS, Chandarlapaty S, Pagano NC, et al. mTOR kinase inhibition causes feedback-dependent biphasic regulation of AKT signaling. Cancer Discov 2011; 1: 248-59.
-
(2011)
Cancer Discov
, vol.1
, pp. 248-259
-
-
Rodrik-Outmezguine, V.S.1
Chandarlapaty, S.2
Pagano, N.C.3
-
14
-
-
77956579297
-
A phase I study of the oral mTOR inhibitor ridaforolimus (RIDA) in combination with the IGF-1R antibody dalotozumab (DALO) in patients (pts) with advanced solid tumors
-
Di Cosimo S, Bendell JC, Cervantes-Ruiperez A, et al. A phase I study of the oral mTOR inhibitor ridaforolimus (RIDA) in combination with the IGF-1R antibody dalotozumab (DALO) in patients (pts) with advanced solid tumors. Proc ASCO Meeting Abstr 2010; 28: 3008.
-
(2010)
Proc ASCO Meeting Abstr
, vol.28
, pp. 3008
-
-
Di Cosimo, S.1
Bendell, J.C.2
Cervantes-Ruiperez, A.3
-
15
-
-
34249779568
-
Temsirolimus, interferon alfa, or both for advanced renal-cell carcinoma
-
Hudes G, Carducci M, Tomczak P, et al. Temsirolimus, interferon alfa, or both for advanced renal-cell carcinoma. N Engl J Med 2007; 356: 2271-81.
-
(2007)
N Engl J Med
, vol.356
, pp. 2271-2281
-
-
Hudes, G.1
Carducci, M.2
Tomczak, P.3
-
16
-
-
68949102180
-
Phase III study to evaluate temsirolimus compared with investigator's choice therapy for the treatment of relapsed or refractory mantle cell lymphoma
-
Hess G, Herbrecht R, Romaguera J, et al. Phase III study to evaluate temsirolimus compared with investigator's choice therapy for the treatment of relapsed or refractory mantle cell lymphoma. J Clin Oncol 2009; 27: 3822-9.
-
(2009)
J Clin Oncol
, vol.27
, pp. 3822-3829
-
-
Hess, G.1
Herbrecht, R.2
Romaguera, J.3
-
17
-
-
79851500081
-
Everolimus for advanced pancreatic neuroendocrine tumors
-
Yao JC, Shah MH, Ito T, et al. Everolimus for advanced pancreatic neuroendocrine tumors. N Engl J Med 2011; 364: 514-23.
-
(2011)
N Engl J Med
, vol.364
, pp. 514-523
-
-
Yao, J.C.1
Shah, M.H.2
Ito, T.3
-
18
-
-
77956227464
-
Phase 3 trial of everolimus for metastatic renal cell carcinoma: Final results and analysis of prognostic factors
-
Motzer RJ, Escudier B, Oudard S, et al. Phase 3 trial of everolimus for metastatic renal cell carcinoma: final results and analysis of prognostic factors. Cancer 2010; 116: 4256-65.
-
(2010)
Cancer
, vol.116
, pp. 4256-4265
-
-
Motzer, R.J.1
Escudier, B.2
Oudard, S.3
-
19
-
-
8444224619
-
Balancing Akt with S6K: Implications for both metabolic diseases and tumorigenesis
-
Manning BD. Balancing Akt with S6K: implications for both metabolic diseases and tumorigenesis. J Cell Biol 2004; 167: 399-403.
-
(2004)
J Cell Biol
, vol.167
, pp. 399-403
-
-
Manning, B.D.1
-
20
-
-
39149123820
-
A vascular targeted pan phosphoinositide 3-kinase inhibitor prodrug, SF1126, with antitumor and antiangiogenic activity
-
Garlich JR, De P, Dey N, et al. A vascular targeted pan phosphoinositide 3-kinase inhibitor prodrug, SF1126, with antitumor and antiangiogenic activity. Cancer Res 2008; 68: 206-15.
-
(2008)
Cancer Res
, vol.68
, pp. 206-215
-
-
Garlich, J.R.1
De, P.2
Dey, N.3
-
21
-
-
80054751392
-
Phase I study of the multikinase prodrug SF1126 in solid tumors and B-cell malignancies
-
Mahadevan D, Chiorean EG, Harris W, et al. Phase I study of the multikinase prodrug SF1126 in solid tumors and B-cell malignancies. ASCO Meeting Abstr 2011; 29: 3015.
-
(2011)
ASCO Meeting Abstr
, vol.29
, pp. 3015
-
-
Mahadevan, D.1
Chiorean, E.G.2
Harris, W.3
-
22
-
-
51049109033
-
Identification and characterization of NVP-BEZ235, a new orally available dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor with potent in vivo antitumor activity
-
Maira SM, Stauffer F, Brueggen J, et al. Identification and characterization of NVP-BEZ235, a new orally available dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor with potent in vivo antitumor activity. Mol Cancer Ther 2008; 7: 1851-63.
-
(2008)
Mol Cancer Ther
, vol.7
, pp. 1851-1863
-
-
Maira, S.M.1
Stauffer, F.2
Brueggen, J.3
-
23
-
-
57349194139
-
Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers
-
Engelman JA, Chen L, Tan X, et al. Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers. Nat Med 2008; 14: 1351-6.
-
(2008)
Nat Med
, vol.14
, pp. 1351-1356
-
-
Engelman, J.A.1
Chen, L.2
Tan, X.3
-
24
-
-
51849111524
-
NVP-BEZ235, a dual PI3K/mTOR inhibitor, prevents PI3K signaling and inhibits the growth of cancer cells with activating PI3K mutations
-
Serra V, Markman B, Scaltriti M, et al. NVP-BEZ235, a dual PI3K/mTOR inhibitor, prevents PI3K signaling and inhibits the growth of cancer cells with activating PI3K mutations. Cancer Res 2008; 68: 8022-30.
-
(2008)
Cancer Res
, vol.68
, pp. 8022-8030
-
-
Serra, V.1
Markman, B.2
Scaltriti, M.3
-
25
-
-
84856988295
-
A dose-escalation study with the novel formulation of the oral pan-class I PI3K inhibitor BEZ235, solid dispersion system (SDS) sachet, in patients with advanced solid tumors
-
Peyton JD, Rodon Ahnert J, Burris H, et al. A dose-escalation study with the novel formulation of the oral pan-class I PI3K inhibitor BEZ235, solid dispersion system (SDS) sachet, in patients with advanced solid tumors. ASCO Meeting Abstr 2011; 29: 3066.
-
(2011)
ASCO Meeting Abstr
, vol.29
, pp. 3066
-
-
Peyton, J.D.1
Rodon Ahnert, J.2
Burris, H.3
-
26
-
-
77956602070
-
First-in-human phase I study of the oral PI3K inhibitor BEZ235 in patients (pts) with advanced solid tumors
-
Burris H, Rodon J, Sharma S, et al. First-in-human phase I study of the oral PI3K inhibitor BEZ235 in patients (pts) with advanced solid tumors. ASCO Meeting Abstr 2010; 28: 3005.
-
(2010)
ASCO Meeting Abstr
, vol.28
, pp. 3005
-
-
Burris, H.1
Rodon, J.2
Sharma, S.3
-
27
-
-
84874661918
-
A phase I/IB doseescalation study of BEZ235 in combination with trastuzumab in patients with PI3-kinase or PTEN altered HER2+ metastatic breast cancer
-
Krop IE, Saura C, Rodon Ahnert J, et al. A phase I/IB doseescalation study of BEZ235 in combination with trastuzumab in patients with PI3-kinase or PTEN altered HER2+ metastatic breast cancer. ASCO Meeting Abstr 2012; 30: 508.
-
(2012)
ASCO Meeting Abstr
, vol.30
, pp. 508
-
-
Krop, I.E.1
Saura, C.2
Rodon Ahnert, J.3
-
28
-
-
70350176755
-
A phase I doseescalation study of the safety, pharmacokinetics (PK), and pharmacodynamics of XL765, a PI3K/TORC1/TORC2 inhibitor administered orally to patients (pts) with advanced solid tumors
-
LoRusso P, Markman B, Tabernero J, et al. A phase I doseescalation study of the safety, pharmacokinetics (PK), and pharmacodynamics of XL765, a PI3K/TORC1/TORC2 inhibitor administered orally to patients (pts) with advanced solid tumors. ASCO Meeting Abstr 2009; 27: 3502.
-
(2009)
ASCO Meeting Abstr
, vol.27
, pp. 3502
-
-
LoRusso, P.1
Markman, B.2
Tabernero, J.3
-
29
-
-
83355163329
-
GDC-0980 is a novel class I PI3K/mTOR kinase inhibitor with robust activity in cancer models driven by the PI3K pathway
-
Wallin JJ, Edgar KA, Guan J, et al. GDC-0980 is a novel class I PI3K/mTOR kinase inhibitor with robust activity in cancer models driven by the PI3K pathway. Mol Cancer Ther 2011; 10: 2426-36.
-
(2011)
Mol Cancer Ther
, vol.10
, pp. 2426-2436
-
-
Wallin, J.J.1
Edgar, K.A.2
Guan, J.3
-
30
-
-
80054740282
-
A first-in-human phase I study to evaluate GDC-0980, an oral PI3K/mTOR inhibitor, administered QD in patients with advanced solid tumors
-
Wagner AJ, Bendell JC, Dolly S, et al. A first-in-human phase I study to evaluate GDC-0980, an oral PI3K/mTOR inhibitor, administered QD in patients with advanced solid tumors. ASCO Meeting Abstr 2011; 29: 3020.
-
(2011)
ASCO Meeting Abstr
, vol.29
, pp. 3020
-
-
Wagner, A.J.1
Bendell, J.C.2
Dolly, S.3
-
31
-
-
81055149891
-
PF-04691502, a potent and selective oral inhibitor of PI3K and mTOR kinases with antitumor activity
-
Yuan J, Mehta PP, Yin MJ, et al. PF-04691502, a potent and selective oral inhibitor of PI3K and mTOR kinases with antitumor activity. Mol Cancer Ther 2011; 10: 2189-99.
-
(2011)
Mol Cancer Ther
, vol.10
, pp. 2189-2199
-
-
Yuan, J.1
Mehta, P.P.2
Yin, M.J.3
-
32
-
-
84876725817
-
Abstract B163: First-inpatient study of PF-04691502, a small molecule intravenous dual inhibitor of PI3K and mTOR in patients with advanced cancer: Update on safety, efficacy, and pharmacology
-
Millham R, Houk B, Borzillo G, et al. Abstract B163: First-inpatient study of PF-04691502, a small molecule intravenous dual inhibitor of PI3K and mTOR in patients with advanced cancer: Update on safety, efficacy, and pharmacology. Mol Cancer Ther 2011; 10: B163.
-
(2011)
Mol Cancer Ther
, vol.10
-
-
Millham, R.1
Houk, B.2
Borzillo, G.3
-
33
-
-
84876727756
-
Abstract A167: First-inpatient study of PF-05212384, a small molecule intravenous dual inhibitor of PI3K and mTOR in patients with advanced cancer: Update on safety, efficacy, and pharmacology
-
Millham R, Houk B, Borzillo G, et al. Abstract A167: First-inpatient study of PF-05212384, a small molecule intravenous dual inhibitor of PI3K and mTOR in patients with advanced cancer: Update on safety, efficacy, and pharmacology. Mol Cancer Ther 2011; 10: A167.
-
(2011)
Mol Cancer Ther
, vol.10
-
-
Millham, R.1
Houk, B.2
Borzillo, G.3
-
34
-
-
80054748915
-
Phase I first-inhuman study of the PI3 kinase inhibitor GSK2126458 (GSK458) in patients with advanced solid tumors (study P3K112826)
-
Munster PN, van der Noll R, Voest EE, et al. Phase I first-inhuman study of the PI3 kinase inhibitor GSK2126458 (GSK458) in patients with advanced solid tumors (study P3K112826). ASCO Meeting Abstr 2011; 29: 3018.
-
(2011)
ASCO Meeting Abstr
, vol.29
, pp. 3018
-
-
Munster, P.N.1
van der Noll, R.2
Voest, E.E.3
-
35
-
-
85039654947
-
Abstract B160: PWT33597 promotes apoptosis in tumor cells through balanced dual inhibition of PI3K alpha and mTOR
-
Matthews DJ, Ventura R, Tai A, Holst C, O'Farrell M. Abstract B160: PWT33597 promotes apoptosis in tumor cells through balanced dual inhibition of PI3K alpha and mTOR. Mol Cancer Ther 2011; 10: B160.
-
(2011)
Mol Cancer Ther
, vol.10
-
-
Matthews, D.J.1
Ventura, R.2
Tai, A.3
Holst, C.4
O'Farrell, M.5
-
36
-
-
84876214814
-
Abstract 3737: The PI3K/mTOR inhibitor PWT33597 regresses 786-0 renal xenografts
-
O'Farrell M, Ventura R, Tai A, Matthews DJ. Abstract 3737: The PI3K/mTOR inhibitor PWT33597 regresses 786-0 renal xenografts. Cancer Research 2012; 72: 3737.
-
(2012)
Cancer Research
, vol.72
, pp. 3737
-
-
O'Farrell, M.1
Ventura, R.2
Tai, A.3
Matthews, D.J.4
-
37
-
-
84856826293
-
Identification and characterization of NVP-BKM120, an orally available pan-class I PI3-kinase inhibitor
-
Maira SM, Pecchi S, Huang A, et al. Identification and characterization of NVP-BKM120, an orally available pan-class I PI3-kinase inhibitor. Mol Cancer Ther 2012; 11: 317-28.
-
(2012)
Mol Cancer Ther
, vol.11
, pp. 317-328
-
-
Maira, S.M.1
Pecchi, S.2
Huang, A.3
-
38
-
-
84864885418
-
Characterization of the mechanism of action of the pan class I PI3K inhibitor NVPBKM120 across a broad range of concentrations
-
Brachmann SM, Kleylein-Sohn J, Gaulis S, et al. Characterization of the mechanism of action of the pan class I PI3K inhibitor NVPBKM120 across a broad range of concentrations. Mol Cancer Ther 2012.
-
(2012)
Mol Cancer Ther
-
-
Brachmann, S.M.1
Kleylein-Sohn, J.2
Gaulis, S.3
-
39
-
-
84856071447
-
Phase I, dose-escalation study of BKM120, an oral pan-Class I PI3K inhibitor, in patients with advanced solid tumors
-
Bendell JC, Rodon J, Burris HA, et al. Phase I, dose-escalation study of BKM120, an oral pan-Class I PI3K inhibitor, in patients with advanced solid tumors. J Clin Oncol 2012; 30: 282-90.
-
(2012)
J Clin Oncol
, vol.30
, pp. 282-290
-
-
Bendell, J.C.1
Rodon, J.2
Burris, H.A.3
-
40
-
-
77956566979
-
A phase I dose-escalation study of XL147 (SAR245408), a PI3K inhibitor administered orally to patients (pts) with advanced malignancies
-
Edelman G, Bedell C, Shapiro G, et al. A phase I dose-escalation study of XL147 (SAR245408), a PI3K inhibitor administered orally to patients (pts) with advanced malignancies. ASCO Meeting Abstr 2010; 28: 3004.
-
(2010)
ASCO Meeting Abstr
, vol.28
, pp. 3004
-
-
Edelman, G.1
Bedell, C.2
Shapiro, G.3
-
41
-
-
4444223702
-
Molecular pharmacology and antitumor activity of PX-866, a novel inhibitor of phosphoinositide-3-kinase signaling
-
Ihle NT, Williams R, Chow S, et al. Molecular pharmacology and antitumor activity of PX-866, a novel inhibitor of phosphoinositide-3-kinase signaling. Mol Cancer Ther 2004; 3: 763-72.
-
(2004)
Mol Cancer Ther
, vol.3
, pp. 763-772
-
-
Ihle, N.T.1
Williams, R.2
Chow, S.3
-
42
-
-
58249120506
-
Mutations in the phosphatidylinositol-3-kinase pathway predict for antitumor activity of the inhibitor PX-866 whereas oncogenic Ras is a dominant predictor for resistance
-
Ihle NT, Lemos R, Jr., Wipf P, et al. Mutations in the phosphatidylinositol-3-kinase pathway predict for antitumor activity of the inhibitor PX-866 whereas oncogenic Ras is a dominant predictor for resistance. Cancer Res 2009; 69: 143-50.
-
(2009)
Cancer Res
, vol.69
, pp. 143-150
-
-
Ihle, N.T.1
Lemos Jr., R.2
Wipf, P.3
-
43
-
-
84864493357
-
A Multicenter Phase 1 Trial of PX-866, an Oral Irreversible Phosphatidylinositol 3-Kinase Inhibitor, in Patients with Advanced Solid Tumors
-
Hong DS, Bowles DW, Falchook GS, et al. A Multicenter Phase 1 Trial of PX-866, an Oral Irreversible Phosphatidylinositol 3-Kinase Inhibitor, in Patients with Advanced Solid Tumors. Clin Cancer Res 2012; 18(15): 4173-82.
-
(2012)
Clin Cancer Res
, vol.18
, Issue.15
, pp. 4173-4182
-
-
Hong, D.S.1
Bowles, D.W.2
Falchook, G.S.3
-
44
-
-
52449106253
-
The identification of 2-(1H-indazol-4-yl)-6-(4-methanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer
-
Folkes AJ, Ahmadi K, Alderton WK, et al. The identification of 2-(1H-indazol-4-yl)-6-(4-methanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer. J Med Chem 2008; 51: 5522-32.
-
(2008)
J Med Chem
, vol.51
, pp. 5522-5532
-
-
Folkes, A.J.1
Ahmadi, K.2
Alderton, W.K.3
-
45
-
-
84861963385
-
A phase I doseescalation study to evaluate GDC-0941, a pan-PI3K inhibitor, administered QD or BID in patients with advanced or metastatic solid tumors
-
Von Hoff DD, LoRusso P, Demetri GD, et al. A phase I doseescalation study to evaluate GDC-0941, a pan-PI3K inhibitor, administered QD or BID in patients with advanced or metastatic solid tumors. ASCO Meeting Abstr 2011; 29: 3052.
-
(2011)
ASCO Meeting Abstr
, vol.29
, pp. 3052
-
-
von Hoff, D.D.1
LoRusso, P.2
Demetri, G.D.3
-
46
-
-
84861992072
-
A phase I study evaluating GDC-0941, an oral phosphoinositide-3 kinase (PI3K) inhibitor, in patients with advanced solid tumors or multiple myeloma
-
Moreno Garcia V, Baird RD, Shah KJ, et al. A phase I study evaluating GDC-0941, an oral phosphoinositide-3 kinase (PI3K) inhibitor, in patients with advanced solid tumors or multiple myeloma. ASCO Meeting Abstr 2011; 29: 3021.
-
(2011)
ASCO Meeting Abstr
, vol.29
, pp. 3021
-
-
Moreno Garcia, V.1
Baird, R.D.2
Shah, K.J.3
-
47
-
-
79960253536
-
A first-in-human phase I study of intravenous PI3K inhibitor BAY 80-6946 in patients with advanced solid tumors: Results of dose-escalation phase
-
Patnaik A, Appleman LJ, Mountz JM, et al. A first-in-human phase I study of intravenous PI3K inhibitor BAY 80-6946 in patients with advanced solid tumors: Results of dose-escalation phase. ASCO Meeting Abstr 2011; 29: 3035.
-
(2011)
ASCO Meeting Abstr
, vol.29
, pp. 3035
-
-
Patnaik, A.1
Appleman, L.J.2
Mountz, J.M.3
-
48
-
-
84876725174
-
Phase I study of intravenous PI3K inhibitor BAY 80-6946: Activity in patients (pts) with advanced solid tumors and non-Hodgkin lymphoma treated in MTD expansion cohorts
-
Lotze MT, Appleman LJ, Ramanathan RK, et al. Phase I study of intravenous PI3K inhibitor BAY 80-6946: Activity in patients (pts) with advanced solid tumors and non-Hodgkin lymphoma treated in MTD expansion cohorts. ASCO Meeting Abstr 2012; 30: 3019.
-
(2012)
ASCO Meeting Abstr
, vol.30
, pp. 3019
-
-
Lotze, M.T.1
Appleman, L.J.2
Ramanathan, R.K.3
-
49
-
-
79955983369
-
The selective class I PI3K inhibitor CH5132799 targets human cancers harboring oncogenic PIK3CA mutations
-
Tanaka H, Yoshida M, Tanimura H, et al. The selective class I PI3K inhibitor CH5132799 targets human cancers harboring oncogenic PIK3CA mutations. Clin Cancer Res 2011; 17: 3272-81.
-
(2011)
Clin Cancer Res
, vol.17
, pp. 3272-3281
-
-
Tanaka, H.1
Yoshida, M.2
Tanimura, H.3
-
50
-
-
84874648611
-
A pharmacokinetic (PK) pharmacodynamic (PD) driven first-in-human study of the oral class I PI3K inhibitor CH5132799, in patients with advanced solid tumors
-
Omlin AG, Spicer JF, Sarker D, et al. A pharmacokinetic (PK) pharmacodynamic (PD) driven first-in-human study of the oral class I PI3K inhibitor CH5132799, in patients with advanced solid tumors. ASCO Meeting Abstr 2012; 30: 3022.
-
(2012)
ASCO Meeting Abstr
, vol.30
, pp. 3022
-
-
Omlin, A.G.1
Spicer, J.F.2
Sarker, D.3
-
51
-
-
34548189038
-
ZSTK474 is an ATP-competitive inhibitor of class I phosphatidylinositol 3 kinase isoforms
-
Kong D, Yamori T. ZSTK474 is an ATP-competitive inhibitor of class I phosphatidylinositol 3 kinase isoforms. Cancer Sci 2007; 98: 1638-42.
-
(2007)
Cancer Sci
, vol.98
, pp. 1638-1642
-
-
Kong, D.1
Yamori, T.2
-
52
-
-
77952931508
-
Abstract B148: INK128 is a potent and selective TORC1/2 inhibitor with broad oral antitumor activity
-
Jessen K, Wang S, Kessler L, et al. Abstract B148: INK128 is a potent and selective TORC1/2 inhibitor with broad oral antitumor activity. Mol Cancer Ther 2009; 8: B148.
-
(2009)
Mol Cancer Ther
, vol.8
-
-
Jessen, K.1
Wang, S.2
Kessler, L.3
-
53
-
-
80051590039
-
Preclinical characterization of OSI-027, a potent and selective inhibitor of mTORC1 and mTORC2: Distinct from rapamycin
-
Bhagwat SV, Gokhale PC, Crew AP, et al. Preclinical characterization of OSI-027, a potent and selective inhibitor of mTORC1 and mTORC2: distinct from rapamycin. Mol Cancer Ther 2011; 10: 1394-406.
-
(2011)
Mol Cancer Ther
, vol.10
, pp. 1394-1406
-
-
Bhagwat, S.V.1
Gokhale, P.C.2
Crew, A.P.3
-
54
-
-
79951651465
-
First-in-human phase I study exploring three schedules of OSI-027, a novel small molecule TORC1/TORC2 inhibitor, in patients with advanced solid tumors and lymphoma
-
Tan DS, Dumez H, Olmos D, et al. First-in-human phase I study exploring three schedules of OSI-027, a novel small molecule TORC1/TORC2 inhibitor, in patients with advanced solid tumors and lymphoma. ASCO Meeting Abstr 2010; 28: 3006.
-
(2010)
ASCO Meeting Abstr
, vol.28
, pp. 3006
-
-
Tan, D.S.1
Dumez, H.2
Olmos, D.3
-
55
-
-
75149112670
-
AZD8055 is a potent, selective, and orally bioavailable ATP-competitive mammalian target of rapamycin kinase inhibitor with in vitro and in vivo antitumor activity
-
Chresta CM, Davies BR, Hickson I, et al. AZD8055 is a potent, selective, and orally bioavailable ATP-competitive mammalian target of rapamycin kinase inhibitor with in vitro and in vivo antitumor activity. Cancer Res 2010; 70: 288-98.
-
(2010)
Cancer Res
, vol.70
, pp. 288-298
-
-
Chresta, C.M.1
Davies, B.R.2
Hickson, I.3
-
56
-
-
80054752120
-
First results from a phase I trial of AZD8055, a dual mTORC1 and mTORC2 inhibitor
-
Banerji U, Aghajanian C, Raymond E, et al. First results from a phase I trial of AZD8055, a dual mTORC1 and mTORC2 inhibitor. ASCO Meeting Abstr 2011; 29: 3096.
-
(2011)
ASCO Meeting Abstr
, vol.29
, pp. 3096
-
-
Banerji, U.1
Aghajanian, C.2
Raymond, E.3
-
57
-
-
84876703624
-
Abstract 917: AZD2014, a dual mTORC1 and mTORC2 inhibitor is differentiated from allosteric inhibitors of mTORC1 in ER+ breast cancer
-
Guichard SM, Howard Z, Heathcote D, et al. Abstract 917: AZD2014, a dual mTORC1 and mTORC2 inhibitor is differentiated from allosteric inhibitors of mTORC1 in ER+ breast cancer. Cancer Res 2012; 72: 917.
-
(2012)
Cancer Res
, vol.72
, pp. 917
-
-
Guichard, S.M.1
Howard, Z.2
Heathcote, D.3
-
58
-
-
84876276597
-
First-in-human phase I trial of the dual mTORC1 and mTORC2 inhibitor AZD2014 in solid tumors
-
Banerji U, Dean EJ, Gonzalez M, et al. First-in-human phase I trial of the dual mTORC1 and mTORC2 inhibitor AZD2014 in solid tumors. ASCO Meeting Abstr 2012; 30: 3004.
-
(2012)
ASCO Meeting Abstr
, vol.30
, pp. 3004
-
-
Banerji, U.1
Dean, E.J.2
Gonzalez, M.3
-
59
-
-
84874656719
-
Phase I trial of an oral TORC1/TORC2 inhibitor (CC-223) in advanced solid and hematologic cancers
-
Shih KC, Bendell JC, Reinert A, et al. Phase I trial of an oral TORC1/TORC2 inhibitor (CC-223) in advanced solid and hematologic cancers. ASCO Meeting Abstr 2012; 30: 3006.
-
(2012)
ASCO Meeting Abstr
, vol.30
, pp. 3006
-
-
Shih, K.C.1
Bendell, J.C.2
Reinert, A.3
-
60
-
-
83255162603
-
First-in-man clinical trial of the oral pan-AKT inhibitor MK-2206 in patients with advanced solid tumors
-
Yap TA, Yan L, Patnaik A, Fearen I, et al. First-in-man clinical trial of the oral pan-AKT inhibitor MK-2206 in patients with advanced solid tumors. J Clin Oncol 2011; 29: 4688-95.
-
(2011)
J Clin Oncol
, vol.29
, pp. 4688-4695
-
-
Yap, T.A.1
Yan, L.2
Patnaik, A.3
Fearen, I.4
-
61
-
-
80054741601
-
First-in-human phase I study evaluating the safety, pharmacokinetics (PK), and intratumor pharmacodynamics (PD) of the novel, oral, ATP-competitive Akt inhibitor GDC-0068
-
Tabernero J, Saura C, Roda Perez D, et al. First-in-human phase I study evaluating the safety, pharmacokinetics (PK), and intratumor pharmacodynamics (PD) of the novel, oral, ATP-competitive Akt inhibitor GDC-0068. ASCO Meeting Abstr 2011; 29: 3022.
-
(2011)
ASCO Meeting Abstr
, vol.29
, pp. 3022
-
-
Tabernero, J.1
Saura, C.2
Roda Perez, D.3
-
62
-
-
42049115641
-
Characterization of an Akt kinase inhibitor with potent pharmacodynamic and antitumor activity
-
Rhodes N, Heerding DA, Duckett DR, et al. Characterization of an Akt kinase inhibitor with potent pharmacodynamic and antitumor activity. Cancer Res 2008; 68: 2366-74.
-
(2008)
Cancer Res
, vol.68
, pp. 2366-2374
-
-
Rhodes, N.1
Heerding, D.A.2
Duckett, D.R.3
-
63
-
-
80054747639
-
Safety, pharmacokinetics (PK), pharmacodynamics (PD), and clinical activity of the oral AKT inhibitor GSK2141795 (GSK795) in a phase I first-in-human study
-
Burris HA, Siu LL, Infante JR, et al. Safety, pharmacokinetics (PK), pharmacodynamics (PD), and clinical activity of the oral AKT inhibitor GSK2141795 (GSK795) in a phase I first-in-human study. ASCO Meeting Abstr 2011; 29: 3003.
-
(2011)
ASCO Meeting Abstr
, vol.29
, pp. 3003
-
-
Burris, H.A.1
Siu, L.L.2
Infante, J.R.3
-
64
-
-
84862738897
-
Preclinical pharmacology of AZD5363, an inhibitor of AKT: Pharmacodynamics, antitumor activity, and correlation of monotherapy activity with genetic background
-
Davies BR, Greenwood H, Dudley P, et al. Preclinical pharmacology of AZD5363, an inhibitor of AKT: pharmacodynamics, antitumor activity, and correlation of monotherapy activity with genetic background. Mol Cancer Ther 2012; 11: 873-87.
-
(2012)
Mol Cancer Ther
, vol.11
, pp. 873-887
-
-
Davies, B.R.1
Greenwood, H.2
Dudley, P.3
-
65
-
-
84876726023
-
First-in-human phase I study of LY2780301, an oral P70S6K/AKT inhibitor, in patients with refractory solid tumors
-
Calvo E, Benhadji KA, Azaro A, et al. First-in-human phase I study of LY2780301, an oral P70S6K/AKT inhibitor, in patients with refractory solid tumors. ASCO Meeting Abstr 2012; 30: 3005.
-
(2012)
ASCO Meeting Abstr
, vol.30
, pp. 3005
-
-
Calvo, E.1
Benhadji, K.A.2
Azaro, A.3
-
66
-
-
84873338382
-
Final results of a first-in-human phase I trial of PBI-05204, an inhibitor of AKT, FGF-2, NF-Kb, and p70S6K in advanced cancer patients
-
Henary HA, Kurzrock R, Falchook GS, et al. Final results of a first-in-human phase I trial of PBI-05204, an inhibitor of AKT, FGF-2, NF-Kb, and p70S6K in advanced cancer patients. ASCO Meeting Abstr 2011; 29: 3023.
-
(2011)
ASCO Meeting Abstr
, vol.29
, pp. 3023
-
-
Henary, H.A.1
Kurzrock, R.2
Falchook, G.S.3
-
67
-
-
60349088457
-
Perifosine: Update on a novel Akt inhibitor
-
Gills JJ, Dennis PA. Perifosine: update on a novel Akt inhibitor. Curr Oncol Rep 2009; 11: 102-10.
-
(2009)
Curr Oncol Rep
, vol.11
, pp. 102-110
-
-
Gills, J.J.1
Dennis, P.A.2
-
68
-
-
49649087385
-
Essential roles of PI(3)K-p110beta in cell growth, metabolism and tumorigenesis
-
Jia S, Liu Z, Zhang S, et al. Essential roles of PI(3)K-p110beta in cell growth, metabolism and tumorigenesis. Nature 2008; 454: 776-9.
-
(2008)
Nature
, vol.454
, pp. 776-779
-
-
Jia, S.1
Liu, Z.2
Zhang, S.3
-
69
-
-
84875950102
-
Abstract CT-01: BYL719, a next generation PI3K alpha specific inhibitor: Preliminary safety, PK, and efficacy results from the first-in-human study
-
CT-01
-
Juric D, Rodon J, Gonzalez-Angulo AM, et al. Abstract CT-01: BYL719, a next generation PI3K alpha specific inhibitor: Preliminary safety, PK, and efficacy results from the first-in-human study. Cancer Res 2012; 72: CT-01.
-
(2012)
Cancer Res
, vol.72
-
-
Juric, D.1
Rodon, J.2
Gonzalez-Angulo, A.M.3
-
70
-
-
84874294680
-
Abstract A171: A potent and selective PI3K inhibitor, INK1117, targets human cancers harboring oncogenic PIK3CA mutations
-
Jessen K, Kessler L, Kucharski J, et al. Abstract A171: A potent and selective PI3K inhibitor, INK1117, targets human cancers harboring oncogenic PIK3CA mutations. Mol Cancer Ther 2011; 10: A171.
-
(2011)
Mol Cancer Ther
, vol.10
-
-
Jessen, K.1
Kessler, L.2
Kucharski, J.3
-
71
-
-
84875143933
-
Abstract 2913: Identification of GSK2636771, a potent and selective, orally bioavailable inhibitor of phosphatidylinositol 3-kinase-beta (PI3K{alpha}) for the treatment of PTEN deficient tumors
-
Rivero RA, Hardwicke MA. Abstract 2913: Identification of GSK2636771, a potent and selective, orally bioavailable inhibitor of phosphatidylinositol 3-kinase-beta (PI3K{alpha}) for the treatment of PTEN deficient tumors. Cancer Res 2012; 72: 2913.
-
(2012)
Cancer Res
, vol.72
, pp. 2913
-
-
Rivero, R.A.1
Hardwicke, M.A.2
-
72
-
-
78751553221
-
CAL-101, a p110delta selective phosphatidylinositol-3-kinase inhibitor for the treatment of B-cell malignancies, inhibits PI3K signaling and cellular viability
-
Lannutti BJ, Meadows SA, Herman SE, et al. CAL-101, a p110delta selective phosphatidylinositol-3-kinase inhibitor for the treatment of B-cell malignancies, inhibits PI3K signaling and cellular viability. Blood 2011; 117: 591-4.
-
(2011)
Blood
, vol.117
, pp. 591-594
-
-
Lannutti, B.J.1
Meadows, S.A.2
Herman, S.E.3
-
73
-
-
77957203544
-
Interim results from a phase I study of CAL-101, a selective oral inhibitor of phosphatidylinositol 3-kinase p110d isoform, in patients with relapsed or refractory hematologic malignancies
-
Furman RR, Byrd JC, Flinn IW, et al. Interim results from a phase I study of CAL-101, a selective oral inhibitor of phosphatidylinositol 3-kinase p110d isoform, in patients with relapsed or refractory hematologic malignancies. ASCO Meeting Abstr 2010; 28: 3032.
-
(2010)
ASCO Meeting Abstr
, vol.28
, pp. 3032
-
-
Furman, R.R.1
Byrd, J.C.2
Flinn, I.W.3
-
74
-
-
80053079880
-
Phase I study of CAL-101, an isoform-selective inhibitor of phosphatidylinositol 3-kinase P110d, in patients with previously treated chronic lymphocytic leukemia
-
Coutre SE, Byrd JC, Furman RR, et al. Phase I study of CAL-101, an isoform-selective inhibitor of phosphatidylinositol 3-kinase P110d, in patients with previously treated chronic lymphocytic leukemia. ASCO Meeting Abstr 2011; 29: 6631.
-
(2011)
ASCO Meeting Abstr
, vol.29
, pp. 6631
-
-
Coutre, S.E.1
Byrd, J.C.2
Furman, R.R.3
-
75
-
-
81755162797
-
Phosphatidylinositol 3-kinase and antiestrogen resistance in breast cancer
-
Miller TW, Balko JM, Arteaga CL. Phosphatidylinositol 3-kinase and antiestrogen resistance in breast cancer. J Clin Oncol 2011; 29: 4452-61.
-
(2011)
J Clin Oncol
, vol.29
, pp. 4452-4461
-
-
Miller, T.W.1
Balko, J.M.2
Arteaga, C.L.3
-
76
-
-
38849091433
-
Tamoxifen resistance in breast tumors is driven by growth factor receptor signaling with repression of classic estrogen receptor genomic function
-
Massarweh S, Osborne CK, Creighton CJ, et al. Tamoxifen resistance in breast tumors is driven by growth factor receptor signaling with repression of classic estrogen receptor genomic function. Cancer Res 2008; 68: 826-33.
-
(2008)
Cancer Res
, vol.68
, pp. 826-833
-
-
Massarweh, S.1
Osborne, C.K.2
Creighton, C.J.3
-
77
-
-
67549088394
-
Determination of HER2 phosphorylation at tyrosine 1221/1222 improves prediction of poor survival for breast cancer patients with hormone receptor-positive tumors
-
Frogne T, Laenkholm AV, Lyng MB, Henriksen KL, Lykkesfeldt AE. Determination of HER2 phosphorylation at tyrosine 1221/1222 improves prediction of poor survival for breast cancer patients with hormone receptor-positive tumors. Breast Cancer Res 2009; 11: R11.
-
(2009)
Breast Cancer Res
, vol.11
-
-
Frogne, T.1
Laenkholm, A.V.2
Lyng, M.B.3
Henriksen, K.L.4
Lykkesfeldt, A.E.5
-
78
-
-
77954974573
-
Hyperactivation of phosphatidylinositol-3 kinase promotes escape from hormone dependence in estrogen receptor-positive human breast cancer
-
Miller TW, Hennessy BT, Gonzalez-Angulo AM, et al. Hyperactivation of phosphatidylinositol-3 kinase promotes escape from hormone dependence in estrogen receptor-positive human breast cancer. J Clin Invest 2010; 120: 2406-13.
-
(2010)
J Clin Invest
, vol.120
, pp. 2406-2413
-
-
Miller, T.W.1
Hennessy, B.T.2
Gonzalez-Angulo, A.M.3
-
79
-
-
33748068094
-
Mechanisms of tumor regression and resistance to estrogen deprivation and fulvestrant in a model of estrogen receptor-positive, HER-2/neu-positive breast cancer
-
Massarweh S, Osborne CK, Jiang S, et al. Mechanisms of tumor regression and resistance to estrogen deprivation and fulvestrant in a model of estrogen receptor-positive, HER-2/neu-positive breast cancer. Cancer Res 2006; 66: 8266-73.
-
(2006)
Cancer Res
, vol.66
, pp. 8266-8273
-
-
Massarweh, S.1
Osborne, C.K.2
Jiang, S.3
-
80
-
-
33846207899
-
Diverse gene expression and DNA methylation profiles correlate with differential adaptation of breast cancer cells to the antiestrogens tamoxifen and fulvestrant
-
Fan M, Yan PS, Hartman-Frey C, et al. Diverse gene expression and DNA methylation profiles correlate with differential adaptation of breast cancer cells to the antiestrogens tamoxifen and fulvestrant. Cancer Res 2006; 66: 11954-66.
-
(2006)
Cancer Res
, vol.66
, pp. 11954-11966
-
-
Fan, M.1
Yan, P.S.2
Hartman-Frey, C.3
-
81
-
-
34249050833
-
Inhibition of the phosphatidylinositol 3-kinase/Akt pathway improves response of long-term estrogen-deprived breast cancer xenografts to antiestrogens
-
Sabnis G, Goloubeva O, Jelovac D, Schayowitz A, Brodie A. Inhibition of the phosphatidylinositol 3-kinase/Akt pathway improves response of long-term estrogen-deprived breast cancer xenografts to antiestrogens. Clin Cancer Res 2007; 13: 2751-7.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 2751-2757
-
-
Sabnis, G.1
Goloubeva, O.2
Jelovac, D.3
Schayowitz, A.4
Brodie, A.5
-
82
-
-
84860390340
-
Preclinical modeling of combined phosphatidylinositol-3-kinase inhibition with endocrine therapy for estrogen receptor-positive breast cancer
-
Sanchez CG, Ma CX, Crowder RJ, et al. Preclinical modeling of combined phosphatidylinositol-3-kinase inhibition with endocrine therapy for estrogen receptor-positive breast cancer. Breast Cancer Res 2011; 13: R21.
-
(2011)
Breast Cancer Res
, vol.13
-
-
Sanchez, C.G.1
Ma, C.X.2
Crowder, R.J.3
-
83
-
-
82055187255
-
ERalpha-dependent E2F transcription can mediate resistance to estrogen deprivation in human breast cancer
-
Miller TW, Balko JM, Fox EM, et al. ERalpha-dependent E2F transcription can mediate resistance to estrogen deprivation in human breast cancer. Cancer Discov 2011; 1: 338-51.
-
(2011)
Cancer Discov
, vol.1
, pp. 338-351
-
-
Miller, T.W.1
Balko, J.M.2
Fox, E.M.3
-
84
-
-
22344446415
-
Dual inhibition of mTOR and estrogen receptor signaling in vitro induces cell death in models of breast cancer
-
Boulay A, Rudloff J, Ye J, et al. Dual inhibition of mTOR and estrogen receptor signaling in vitro induces cell death in models of breast cancer. Clin Cancer Res 2005; 11: 5319-28.
-
(2005)
Clin Cancer Res
, vol.11
, pp. 5319-5328
-
-
Boulay, A.1
Rudloff, J.2
Ye, J.3
-
85
-
-
65949110376
-
PIK3CA and PIK3CB inhibition produce synthetic lethality when combined with estrogen deprivation in estrogen receptor-positive breast cancer
-
Crowder RJ, Phommaly C, Tao Y, et al. PIK3CA and PIK3CB inhibition produce synthetic lethality when combined with estrogen deprivation in estrogen receptor-positive breast cancer. Cancer Res 2009; 69: 3955-62.
-
(2009)
Cancer Res
, vol.69
, pp. 3955-3962
-
-
Crowder, R.J.1
Phommaly, C.2
Tao, Y.3
-
86
-
-
84863078767
-
Everolimus in postmenopausal hormone-receptor-positive advanced breast cancer
-
Baselga J, Campone M, Piccart M, et al. Everolimus in postmenopausal hormone-receptor-positive advanced breast cancer. N Engl J Med 2012; 366: 520-9.
-
(2012)
N Engl J Med
, vol.366
, pp. 520-529
-
-
Baselga, J.1
Campone, M.2
Piccart, M.3
-
87
-
-
84864558874
-
Randomized Phase II Trial of Everolimus in Combination With Tamoxifen in Patients With Hormone Receptor-Positive, Human Epidermal Growth Factor Receptor 2-Negative Metastatic Breast Cancer With Prior Exposure to Aromatase Inhibitors: A GINECO Study
-
Bachelot T, Bourgier C, Cropet C, et al. Randomized Phase II Trial of Everolimus in Combination With Tamoxifen in Patients With Hormone Receptor-Positive, Human Epidermal Growth Factor Receptor 2-Negative Metastatic Breast Cancer With Prior Exposure to Aromatase Inhibitors: A GINECO Study. J Clin Oncol 2012.
-
(2012)
J Clin Oncol
-
-
Bachelot, T.1
Bourgier, C.2
Cropet, C.3
-
88
-
-
66849136781
-
Phase II randomized study of neoadjuvant everolimus plus letrozole compared with placebo plus letrozole in patients with estrogen receptor-positive breast cancer
-
Baselga J, Semiglazov V, van Dam P, et al. Phase II randomized study of neoadjuvant everolimus plus letrozole compared with placebo plus letrozole in patients with estrogen receptor-positive breast cancer. J Clin Oncol 2009; 27: 2630-7.
-
(2009)
J Clin Oncol
, vol.27
, pp. 2630-2637
-
-
Baselga, J.1
Semiglazov, V.2
van Dam, P.3
-
89
-
-
56449111358
-
Phosphatidylinositol 3-kinase hyperactivation results in lapatinib resistance that is reversed by the mTOR/phosphatidylinositol 3-kinase inhibitor NVPBEZ235
-
Eichhorn PJ, Gili M, Scaltriti M, et al. Phosphatidylinositol 3-kinase hyperactivation results in lapatinib resistance that is reversed by the mTOR/phosphatidylinositol 3-kinase inhibitor NVPBEZ235. Cancer Res 2008; 68: 9221-30.
-
(2008)
Cancer Res
, vol.68
, pp. 9221-9230
-
-
Eichhorn, P.J.1
Gili, M.2
Scaltriti, M.3
-
90
-
-
35148885729
-
A functional genetic approach identifies the PI3K pathway as a major determinant of trastuzumab resistance in breast cancer
-
Berns K, Horlings HM, Hennessy BT, et al. A functional genetic approach identifies the PI3K pathway as a major determinant of trastuzumab resistance in breast cancer. Cancer Cell 2007; 12: 395-402.
-
(2007)
Cancer Cell
, vol.12
, pp. 395-402
-
-
Berns, K.1
Horlings, H.M.2
Hennessy, B.T.3
-
91
-
-
5144226211
-
PTEN activation contributes to tumor inhibition by trastuzumab, and loss of PTEN predicts trastuzumab resistance in patients
-
Nagata Y, Lan KH, Zhou X, et al. PTEN activation contributes to tumor inhibition by trastuzumab, and loss of PTEN predicts trastuzumab resistance in patients. Cancer Cell 2004; 6: 117-27.
-
(2004)
Cancer Cell
, vol.6
, pp. 117-127
-
-
Nagata, Y.1
Lan, K.H.2
Zhou, X.3
-
92
-
-
79958765919
-
PI3K pathway activation results in low efficacy of both trastuzumab and lapatinib
-
Wang L, Zhang Q, Zhang J, et al. PI3K pathway activation results in low efficacy of both trastuzumab and lapatinib. BMC Cancer 2011; 11: 11:248.
-
(2011)
BMC Cancer
, vol.11
, Issue.11
, pp. 248
-
-
Wang, L.1
Zhang, Q.2
Zhang, J.3
-
93
-
-
80052962211
-
Akt, FoxO and regulation of apoptosis
-
Zhang X, Tang N, Hadden TJ, Rishi AK. Akt, FoxO and regulation of apoptosis. Biochim Biophys Acta 2011; 1813: 1978-86.
-
(2011)
Biochim Biophys Acta
, vol.1813
, pp. 1978-1986
-
-
Zhang, X.1
Tang, N.2
Hadden, T.J.3
Rishi, A.K.4
-
94
-
-
73149101585
-
Inhibition of mammalian target of rapamycin is required for optimal antitumor effect of HER2 inhibitors against HER2-overexpressing cancer cells
-
Miller TW, Forbes JT, Shah C, et al. Inhibition of mammalian target of rapamycin is required for optimal antitumor effect of HER2 inhibitors against HER2-overexpressing cancer cells. Clin Cancer Res 2009; 15: 7266-76.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 7266-7276
-
-
Miller, T.W.1
Forbes, J.T.2
Shah, C.3
-
95
-
-
84860532107
-
Dual mTORC1/2 and HER2 Blockade Results in Antitumor Activity in Preclinical Models of Breast Cancer Resistant to Anti-HER2 Therapy
-
Garcia-Garcia C, Ibrahim YH, Serra V, et al. Dual mTORC1/2 and HER2 Blockade Results in Antitumor Activity in Preclinical Models of Breast Cancer Resistant to Anti-HER2 Therapy. Clin Cancer Res 2012.
-
(2012)
Clin Cancer Res
-
-
Garcia-Garcia, C.1
Ibrahim, Y.H.2
Serra, V.3
-
96
-
-
78650984926
-
Phase I study of everolimus plus weekly paclitaxel and trastuzumab in patients with metastatic breast cancer pretreated with trastuzumab
-
Andre F, Campone M, O'Regan R, et al. Phase I study of everolimus plus weekly paclitaxel and trastuzumab in patients with metastatic breast cancer pretreated with trastuzumab. J Clin Oncol 2010; 28: 5110-5.
-
(2010)
J Clin Oncol
, vol.28
, pp. 5110-5115
-
-
Andre, F.1
Campone, M.2
O'Regan, R.3
-
97
-
-
78650967232
-
Phase I trial of oral mTOR inhibitor everolimus in combination with trastuzumab and vinorelbine in pre-treated patients with HER2-overexpressing metastatic breast cancer
-
Jerusalem G, Fasolo A, Dieras V, et al. Phase I trial of oral mTOR inhibitor everolimus in combination with trastuzumab and vinorelbine in pre-treated patients with HER2-overexpressing metastatic breast cancer. Breast Cancer Res Treat 2011; 125: 447-55.
-
(2011)
Breast Cancer Res Treat
, vol.125
, pp. 447-455
-
-
Jerusalem, G.1
Fasolo, A.2
Dieras, V.3
-
98
-
-
79960599214
-
Phase I/II trial of everolimus (RAD001) and trastuzumab in patients with trastuzumab-resistant, HER2-overexpressing breast cancer
-
Morrow PH, Wulf GM, Booser DJ, et al. Phase I/II trial of everolimus (RAD001) and trastuzumab in patients with trastuzumab-resistant, HER2-overexpressing breast cancer. J Clin Oncol 2010; 28: abstr 1014.
-
(2010)
J Clin Oncol
, vol.28
-
-
Morrow, P.H.1
Wulf, G.M.2
Booser, D.J.3
-
99
-
-
79959712087
-
Ras/Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR inhibitors: Rationale and importance to inhibiting these pathways in human health
-
Chappell WH, Steelman LS, Long JM, et al. Ras/Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR inhibitors: rationale and importance to inhibiting these pathways in human health. Oncotarget 2011; 2: 135-64.
-
(2011)
Oncotarget
, vol.2
, pp. 135-164
-
-
Chappell, W.H.1
Steelman, L.S.2
Long, J.M.3
-
100
-
-
78649831949
-
Crosstalk between the PI3K/mTOR and MEK/ERK pathways involved in the maintenance of self-renewal and tumorigenicity of glioblastoma stem-like cells
-
Sunayama J, Matsuda K, Sato A, et al. Crosstalk between the PI3K/mTOR and MEK/ERK pathways involved in the maintenance of self-renewal and tumorigenicity of glioblastoma stem-like cells. Stem Cells 2010; 28: 1930-9.
-
(2010)
Stem Cells
, vol.28
, pp. 1930-1939
-
-
Sunayama, J.1
Matsuda, K.2
Sato, A.3
-
101
-
-
70449995469
-
Identifying genotypedependent efficacy of single and combined PI3K-and MAPKpathway inhibition in cancer
-
Sos ML, Fischer S, Ullrich R, et al. Identifying genotypedependent efficacy of single and combined PI3K-and MAPKpathway inhibition in cancer. Proc Natl Acad Sci USA 2009; 106: 18351-6.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 18351-18356
-
-
Sos, M.L.1
Fischer, S.2
Ullrich, R.3
-
102
-
-
84863596086
-
MEK Inhibition Leads to PI3K/AKT Activation by Relieving a Negative Feedback on ERBB Receptors
-
Turke AB, Song Y, Costa C, et al. MEK Inhibition Leads to PI3K/AKT Activation by Relieving a Negative Feedback on ERBB Receptors. Cancer Res 2012; 72(13): 3228-37.
-
(2012)
Cancer Res
, vol.72
, Issue.13
, pp. 3228-3237
-
-
Turke, A.B.1
Song, Y.2
Costa, C.3
-
103
-
-
68049085887
-
In vivo antitumor activity of MEK and phosphatidylinositol 3-kinase inhibitors in basal-like breast cancer models
-
Hoeflich KP, O'Brien C, Boyd Z, et al. In vivo antitumor activity of MEK and phosphatidylinositol 3-kinase inhibitors in basal-like breast cancer models. Clin Cancer Res 2009; 15: 4649-64.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 4649-4664
-
-
Hoeflich, K.P.1
O'Brien, C.2
Boyd, Z.3
-
104
-
-
77956280407
-
PIK3CA mutation uncouples tumor growth and cyclin D1 regulation from MEK/ERK and mutant KRAS signaling
-
Halilovic E, She QB, Ye Q, et al. PIK3CA mutation uncouples tumor growth and cyclin D1 regulation from MEK/ERK and mutant KRAS signaling. Cancer Res 2010; 70: 6804-14.
-
(2010)
Cancer Res
, vol.70
, pp. 6804-6814
-
-
Halilovic, E.1
She, Q.B.2
Ye, Q.3
-
105
-
-
66249116702
-
PI3K pathway activation mediates resistance to MEK inhibitors in KRAS mutant cancers
-
Wee S, Jagani Z, Xiang KX, et al. PI3K pathway activation mediates resistance to MEK inhibitors in KRAS mutant cancers. Cancer Res 2009; 69: 4286-93.
-
(2009)
Cancer Res
, vol.69
, pp. 4286-4293
-
-
Wee, S.1
Jagani, Z.2
Xiang, K.X.3
-
106
-
-
84862649725
-
The mitogenactivated protein kinase (MAPK) cascade controls phosphatase and tensin homolog (PTEN) expression through multiple mechanisms
-
Ciuffreda L, Di Sanza C, Cesta Incani U, et al. The mitogenactivated protein kinase (MAPK) cascade controls phosphatase and tensin homolog (PTEN) expression through multiple mechanisms. J Mol Med (Berl) 2012; 90: 667-79.
-
(2012)
J Mol Med (Berl)
, vol.90
, pp. 667-679
-
-
Ciuffreda, L.1
Di Sanza, C.2
Cesta Incani, U.3
-
107
-
-
73349129405
-
Differential induction of apoptosis in HER2 and EGFR addicted cancers following PI3K inhibition
-
Faber AC, Li D, Song Y, et al. Differential induction of apoptosis in HER2 and EGFR addicted cancers following PI3K inhibition. Proc Natl Acad Sci USA 2009; 106: 19503-8.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 19503-19508
-
-
Faber, A.C.1
Li, D.2
Song, Y.3
-
108
-
-
84871183627
-
A first-in-human phase Ib study to evaluate the MEK inhibitor GDC-0973, combined with the pan-PI3K inhibitor GDC-0941, in patients with advanced solid tumors
-
LoRusso P, Shapiro G, Pandya SS, et al. A first-in-human phase Ib study to evaluate the MEK inhibitor GDC-0973, combined with the pan-PI3K inhibitor GDC-0941, in patients with advanced solid tumors. ASCO Meeting Abstr 2012; 30: 2566.
-
(2012)
ASCO Meeting Abstr
, vol.30
, pp. 2566
-
-
LoRusso, P.1
Shapiro, G.2
Pandya, S.S.3
-
109
-
-
84867073064
-
A phase lb, open-label, multicenter, dose-escalation study of the oral pan-PI3K inhibitor BKM120 in combination with the oral MEK1/2 inhibitor GSK1120212 in patients (pts) with selected advanced solid tumors
-
Bedard P, Tabernero J, Kurzrock R, et al. A phase lb, open-label, multicenter, dose-escalation study of the oral pan-PI3K inhibitor BKM120 in combination with the oral MEK1/2 inhibitor GSK1120212 in patients (pts) with selected advanced solid tumors. ASCO Meeting Abstr 2012; 30: 3003.
-
(2012)
ASCO Meeting Abstr
, vol.30
, pp. 3003
-
-
Bedard, P.1
Tabernero, J.2
Kurzrock, R.3
-
110
-
-
80051761743
-
The role of Bcl-2 and its pro-survival relatives in tumourigenesis and cancer therapy
-
Kelly PN, Strasser A. The role of Bcl-2 and its pro-survival relatives in tumourigenesis and cancer therapy. Cell Death Differ 2011; 18: 1414-24.
-
(2011)
Cell Death Differ
, vol.18
, pp. 1414-1424
-
-
Kelly, P.N.1
Strasser, A.2
-
111
-
-
84856989746
-
Inhibition of PI3K/mTOR leads to adaptive resistance in matrix-attached cancer cells
-
Muranen T, Selfors LM, Worster DT, et al. Inhibition of PI3K/mTOR leads to adaptive resistance in matrix-attached cancer cells. Cancer Cell 2012; 21: 227-39.
-
(2012)
Cancer Cell
, vol.21
, pp. 227-239
-
-
Muranen, T.1
Selfors, L.M.2
Worster, D.T.3
-
112
-
-
84859481137
-
Co-targeting of the PI3K pathway improves the response of BRCA1 deficient breast cancer cells to PARP1 inhibition
-
Kimbung S, Biskup E, Johansson I, et al. Co-targeting of the PI3K pathway improves the response of BRCA1 deficient breast cancer cells to PARP1 inhibition. Cancer Lett 2012; 319: 232-41.
-
(2012)
Cancer Lett
, vol.319
, pp. 232-241
-
-
Kimbung, S.1
Biskup, E.2
Johansson, I.3
-
113
-
-
84866709651
-
Combining a PI3K inhibitor with a PARP inhibitor provides an effective therapy for a mouse model of BRCA1-related breast cancer
-
in press
-
Juvekar A, Burga LN, Hu H, et al. Combining a PI3K inhibitor with a PARP inhibitor provides an effective therapy for a mouse model of BRCA1-related breast cancer. Cancer Discov 2012; in press.
-
(2012)
Cancer Discov
-
-
Juvekar, A.1
Burga, L.N.2
Hu, H.3
-
114
-
-
84866681744
-
PI3K inhibition impairs BRCA1/2 expression and sensitizes BRCA proficient triple negative breast cancer to PARP inhibition
-
(in press)
-
Ibrahim YH, García-García C, Serra V, et al. PI3K inhibition impairs BRCA1/2 expression and sensitizes BRCA proficient triple negative breast cancer to PARP inhibition. Cancer Discov 2012; (in press).
-
(2012)
Cancer Discov
-
-
Ibrahim, Y.H.1
García-García, C.2
Serra, V.3
|