-
1
-
-
51849111556
-
PI3K pathway alterations in cancer: Variations on a theme
-
Yuan TL, Cantley LC. PI3K pathway alterations in cancer: variations on a theme. Oncogene 2008;27:5497-510.
-
(2008)
Oncogene
, vol.27
, pp. 5497-5510
-
-
Yuan, T.L.1
Cantley, L.C.2
-
2
-
-
13844273087
-
PI3K-Akt pathway: Its functions and alterations in human cancer
-
DOI 10.1023/B:APPT.0000045801.15585.dd
-
Osaki M, Oshimura M, Ito H. PI3K-Akt pathway: its functions and alterations in human cancer. Apoptosis 2004;9:667-76. (Pubitemid 40941196)
-
(2004)
Apoptosis
, vol.9
, Issue.6
, pp. 667-676
-
-
Osaki, M.1
Oshimura, M.2
Ito, H.3
-
3
-
-
28844448182
-
Oncogenic PI3K deregulates transcription and translation
-
DOI 10.1038/nrc1753
-
Bader AG, Kang S, Zhao L, Vogt PK. Oncogenic PI3K deregulates transcription and translation. Nat Rev Cancer 2005;5:921-9. (Pubitemid 41766781)
-
(2005)
Nature Reviews Cancer
, vol.5
, Issue.12
, pp. 921-929
-
-
Bader, A.G.1
Kang, S.2
Zhao, L.3
Vogt, P.K.4
-
4
-
-
32044466838
-
Exploiting the PI3K/ AKT pathway for cancer drug discovery
-
Hennessy BT, Smith DL, Ram PT, Lu Y, Mills GB. Exploiting the PI3K/ AKT pathway for cancer drug discovery. Nat Rev Drug Discov 2005;4:988-1004.
-
(2005)
Nat Rev Drug Discov
, vol.4
, pp. 988-1004
-
-
Hennessy, B.T.1
Smith, D.L.2
Ram, P.T.3
Lu, Y.4
Mills, G.B.5
-
5
-
-
77956236877
-
PI(3)king apart PTEN's role in cancer
-
Zhang S, Yu D. PI(3)king apart PTEN's role in cancer. Clin Cancer Res 2010;16:4325-30.
-
(2010)
Clin Cancer Res
, vol.16
, pp. 4325-4330
-
-
Zhang, S.1
Yu, D.2
-
6
-
-
28244479028
-
Breast cancer-associated PIK3CA mutations are oncogenic in mammary epithelial cells
-
DOI 10.1158/0008-5472.CAN-05-2612
-
Isakoff SJ, Engelman JA, Irie HY, Luo J, Brachmann SM, Pearline RV, et al. Breast cancer-associated PIK3CA mutations are oncogenic in mammary epithelial cells. Cancer Res 2005;65:10992-1000. (Pubitemid 41713369)
-
(2005)
Cancer Research
, vol.65
, Issue.23
, pp. 10992-11000
-
-
Isakoff, S.J.1
Engelman, J.A.2
Irie, H.Y.3
Luo, J.4
Brachmann, S.M.5
Pearline, R.V.6
Cantley, L.C.7
Brugge, J.S.8
-
7
-
-
80052641904
-
Inactivation of PTEN is responsible for the survival of Hep G2 cells in response to etoposide-induced damage
-
Mukherjee A, Samanta S, Karmakar P. Inactivation of PTEN is responsible for the survival of Hep G2 cells in response to etoposide-induced damage. Mutat Res 2011;715:42-51.
-
(2011)
Mutat Res
, vol.715
, pp. 42-51
-
-
Mukherjee, A.1
Samanta, S.2
Karmakar, P.3
-
8
-
-
49249121067
-
Purification, crystallization and crystallographic analysis of Clostridium thermocellum endo-1,4-beta-D-xylanase 10B in complex with xylohexaose
-
Najmudin S, Pinheiro BA, Romao MJ, Prates JA, Fontes CM. Purification, crystallization and crystallographic analysis of Clostridium thermocellum endo-1,4-beta-D-xylanase 10B in complex with xylohexaose. Acta Crystallogr Sect F Struct Biol Cryst Commun 2008;64:715-8.
-
(2008)
Acta Crystallogr Sect F Struct Biol Cryst Commun
, vol.64
, pp. 715-718
-
-
Najmudin, S.1
Pinheiro, B.A.2
Romao, M.J.3
Prates, J.A.4
Fontes, C.M.5
-
9
-
-
33846694864
-
Activation of Akt predicts poor outcome in neuroblastoma
-
DOI 10.1158/0008-5472.CAN-06-2201
-
Opel D, Poremba C, Simon T, Debatin KM, Fulda S. Activation of Akt predicts poor outcomein neuroblastoma. Cancer Res 2007;67:735-45. (Pubitemid 46192214)
-
(2007)
Cancer Research
, vol.67
, Issue.2
, pp. 735-745
-
-
Opel, D.1
Poremba, C.2
Simon, T.3
Debatin, K.-M.4
Fulda, S.5
-
10
-
-
79959733118
-
Evaluation of the association of PIK3CA mutations and PTEN loss with efficacy of trastuzumab therapy in metastatic breast cancer
-
Razis E,Bobos M, Kotoula V, Eleftheraki AG, Kalofonos HP, Pavlakis K, et al. Evaluation of the association of PIK3CA mutations and PTEN loss with efficacy of trastuzumab therapy in metastatic breast cancer. Breast Cancer Res Treat 2011;128:447-56.
-
(2011)
Breast Cancer Res Treat
, vol.128
, pp. 447-456
-
-
Razis, E.1
Bobos, M.2
Kotoula, V.3
Eleftheraki, A.G.4
Kalofonos, H.P.5
Pavlakis, K.6
-
11
-
-
33846569938
-
Targeting mammalian target of rapamycin (mTOR) for health and diseases
-
DOI 10.1016/j.drudis.2006.12.008, PII S1359644606004910
-
Tsang CK, Qi H, Liu LF, Zheng XF. Targeting mammalian target of rapamycin (mTOR) for health and diseases. Drug Discov Today 2007;12:112-24. (Pubitemid 46176669)
-
(2007)
Drug Discovery Today
, vol.12
, Issue.3-4
, pp. 112-124
-
-
Tsang, C.K.1
Qi, H.2
Liu, L.F.3
Zheng, X.F.S.4
-
12
-
-
70449900928
-
TOR complex 2: A signaling pathway of its own
-
Cybulski N, Hall MN. TOR complex 2: a signaling pathway of its own. Trends Biochem Sci 2009;34:620-7.
-
(2009)
Trends Biochem Sci
, vol.34
, pp. 620-627
-
-
Cybulski, N.1
Hall, M.N.2
-
13
-
-
72049117072
-
Mammalian target of rapamycin: Discovery of rapamycin reveals a signaling pathway important for normal and cancer cell growth
-
Gibbons JJ, Abraham RT, Yu K. Mammalian target of rapamycin: discovery of rapamycin reveals a signaling pathway important for normal and cancer cell growth. Semin Oncol 2009;36(Suppl 3): S3-17.
-
(2009)
Semin Oncol
, vol.36
, Issue.SUPPL. 3
-
-
Gibbons, J.J.1
Abraham, R.T.2
Yu, K.3
-
14
-
-
52449106253
-
The identification of 2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin- 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, Alix S, Baker SJ, Box G, et al. The identification of 2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin- 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
Alix, S.4
Baker, S.J.5
Box, G.6
-
15
-
-
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, Furet P, Schnell C, Fritsch C, 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
Furet, P.4
Schnell, C.5
Fritsch, C.6
-
17
-
-
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, Cavet G, Guerrero S, Jung K, 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
Cavet, G.4
Guerrero, S.5
Jung, K.6
-
18
-
-
65549165975
-
Genetic alterations and oncogenic pathways associated with breast cancer subtypes
-
Hu X, Stern HM, Ge L, O'Brien C, Haydu L, Honchell CD, et al. Genetic alterations and oncogenic pathways associated with breast cancer subtypes. Mol Cancer Res 2009;7:511-22.
-
(2009)
Mol Cancer Res
, vol.7
, pp. 511-522
-
-
Hu, X.1
Stern, H.M.2
Ge, L.3
O'Brien, C.4
Haydu, L.5
Honchell, C.D.6
-
19
-
-
77954645651
-
-
WO2008/073785
-
Castanedo GD, Dotson J, Goldsmith R, Gunzner J, Heffron T, Mathieu S, et al. Inventor phosphoinositide 3-kinase inhibitor compounds and methods of use. 2008;WO2008/073785:A2.
-
(2008)
Inventor Phosphoinositide 3-kinase Inhibitor Compounds and Methods of Use
-
-
Castanedo, G.D.1
Dotson, J.2
Goldsmith, R.3
Gunzner, J.4
Heffron, T.5
Mathieu, S.6
-
20
-
-
34250823572
-
Pharmacologic characterization of a potent inhibitor of class I phosphatidylinositide 3-kinases
-
DOI 10.1158/0008-5472.CAN-06-4615
-
Raynaud FI, Eccles S, Clarke PA, Hayes A, Nutley B, Alix S, et al. Pharmacologic characterization of a potent inhibitor of class I phosphatidylinositide 3-kinases. Cancer Res 2007;67:5840-50. (Pubitemid 46985018)
-
(2007)
Cancer Research
, vol.67
, Issue.12
, pp. 5840-5850
-
-
Raynaud, F.I.1
Eccles, S.2
Clarke, P.A.3
Hayes, A.4
Nutley, B.5
Alix, S.6
Henley, A.7
Di-Stefano, F.8
Ahmad, Z.9
Guillard, S.10
Bjerke, L.M.11
Kelland, L.12
Valenti, M.13
Patterson, L.14
Gowan, S.15
Brandon, A.D.H.16
Hayakawa, M.17
Kaizawa, H.18
Koizumi, T.19
Ohishi, T.20
Patel, S.21
Saghir, N.22
Parker, P.23
Waterfield, M.24
Workman, P.25
more..
-
21
-
-
0029071264
-
TOR kinase domains are required for two distinct functions, only one of which is inhibited by rapamycin
-
Zheng XF, Florentino D, Chen J, Crabtree GR, Schreiber SL. TOR kinase domains are required for two distinct functions, only one of which is inhibited by rapamycin. Cell 1995;82:121-30.
-
(1995)
Cell
, vol.82
, pp. 121-130
-
-
Zheng, X.F.1
Florentino, D.2
Chen, J.3
Crabtree, G.R.4
Schreiber, S.L.5
-
22
-
-
77954755623
-
Predictive biomarkers of sensitivity to the phosphatidylinositol 30 kinase inhibitor GDC-0941 in breast cancer preclinical models
-
O'Brien C, Wallin JJ, Sampath D, GuhaThakurta D, Savage H, Punnoose EA, et al. Predictive biomarkers of sensitivity to the phosphatidylinositol 30 kinase inhibitor GDC-0941 in breast cancer preclinical models. Clin Cancer Res 2010;16:3670-83.
-
(2010)
Clin Cancer Res
, vol.16
, pp. 3670-3683
-
-
O'Brien, C.1
Wallin, J.J.2
Sampath, D.3
GuhaThakurta, D.4
Savage, H.5
Punnoose, E.A.6
-
23
-
-
9444236895
-
Minireview: Cyclin D1: Normal and abnormal functions
-
DOI 10.1210/en.2004-0959
-
Fu M, Wang C, Li Z, Sakamaki T, Pestell RG. Minireview: Cyclin D1: normal and abnormal functions. Endocrinology 2004;145:5439-47. (Pubitemid 39564581)
-
(2004)
Endocrinology
, vol.145
, Issue.12
, pp. 5439-5447
-
-
Fu, M.1
Wang, C.2
Li, Z.3
Sakamaki, T.4
Pestell, R.G.5
-
24
-
-
0032509239
-
Importance of poly(ADP-ribose) polymerase and its cleavage in apoptosis: Lesson from an uncleavable mutant
-
DOI 10.1074/jbc.273.50.33533
-
Oliver FJ, de la Rubia G, Rolli V, Ruiz-Ruiz MC, de Murcia G, Murcia JM. Importance of poly(ADP-ribose) polymerase and its cleavage in apoptosis. Lesson from an uncleavable mutant. J Biol Chem 1998;273: 33533-9. (Pubitemid 29005737)
-
(1998)
Journal of Biological Chemistry
, vol.273
, Issue.50
, pp. 33533-33539
-
-
Oliver, F.J.1
De La, R.G.2
Rolli, V.3
Ruiz-Ruiz, M.C.4
De Murcia, G.5
Menissier-De, M.J.6
-
26
-
-
77956586823
-
Nuclear phospho-Akt increase predicts synergy of PI3K inhibition and doxorubicin in breast and ovarian cancer
-
Wallin JJ, Guan J, Prior WW, Edgar KA, Kassees R, Sampath D, et al. Nuclear phospho-Akt increase predicts synergy of PI3K inhibition and doxorubicin in breast and ovarian cancer. Sci Transl Med 2010;2: 48ra66.
-
(2010)
Sci Transl Med
, vol.2
-
-
Wallin, J.J.1
Guan, J.2
Prior, W.W.3
Edgar, K.A.4
Kassees, R.5
Sampath, D.6
-
27
-
-
28144445570
-
Docetaxel: A review of its use in metastatic breast cancer
-
DOI 10.2165/00003495-200565170-00007
-
Lyseng-Williamson KA, Fenton C. Docetaxel: a review of its use in metastatic breast cancer. Drugs 2005;65:2513-31. (Pubitemid 41697318)
-
(2005)
Drugs
, vol.65
, Issue.17
, pp. 2513-2531
-
-
Lyseng-Williamson, K.A.1
Fenton, C.2
-
28
-
-
77950355502
-
Pharmacogenomics of taxane/platinum therapy in ovarian cancer
-
Marsh S. Pharmacogenomics of taxane/platinum therapy in ovarian cancer. Int J Gynecol Cancer 2009;19(Suppl 2):S30-4.
-
(2009)
Int J Gynecol Cancer
, vol.19
, Issue.SUPPL. 2
-
-
Marsh, S.1
-
29
-
-
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, Harding T, Consulich S, Critchlow SE, 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
Harding, T.4
Consulich, S.5
Critchlow, S.E.6
|