-
1
-
-
79952284127
-
Hallmarks of cancer: the next generation
-
COI: 1:CAS:528:DC%2BC3MXjsFeqtrk%3D, PID: 21376230
-
Hanahan D, Weinberg RA. Hallmarks of cancer: the next generation. Cell. 2011;144:646–74.
-
(2011)
Cell
, vol.144
, pp. 646-674
-
-
Hanahan, D.1
Weinberg, R.A.2
-
2
-
-
84903843882
-
Molecular pathways: CDK4 inhibitors for cancer therapy
-
COI: 1:CAS:528:DC%2BC2cXhtVKksr3O, PID: 24795392
-
Dickson MA. Molecular pathways: CDK4 inhibitors for cancer therapy. Clin Cancer Res. 2014;20:3379–83.
-
(2014)
Clin Cancer Res
, vol.20
, pp. 3379-3383
-
-
Dickson, M.A.1
-
3
-
-
84905699926
-
Palbociclib: an evidence-based review of its potential in the treatment of breast cancer
-
COI: 1:CAS:528:DC%2BC2cXhvFSksLnO
-
Cadoo KA, Gucalp A, Traina TA. Palbociclib: an evidence-based review of its potential in the treatment of breast cancer. Breast Cancer (Dove Med Press). 2014;6:123–33.
-
(2014)
Breast Cancer (Dove Med Press)
, vol.6
, pp. 123-133
-
-
Cadoo, K.A.1
Gucalp, A.2
Traina, T.A.3
-
4
-
-
0001510491
-
The RB and p53 pathways in cancer
-
COI: 1:CAS:528:DC%2BD38XmslSks7s%3D, PID: 12204530
-
Sherr CJ, McCormick F. The RB and p53 pathways in cancer. Cancer Cell. 2002;2:103–12.
-
(2002)
Cancer Cell
, vol.2
, pp. 103-112
-
-
Sherr, C.J.1
McCormick, F.2
-
5
-
-
0027280084
-
Expression and amplification of cyclin genes in human breast cancer
-
COI: 1:CAS:528:DyaK3sXlslymtrs%3D, PID: 8336939
-
Buckley MF, Sweeney KJ, Hamilton JA, et al. Expression and amplification of cyclin genes in human breast cancer. Oncogene. 1993;8:2127–33.
-
(1993)
Oncogene
, vol.8
, pp. 2127-2133
-
-
Buckley, M.F.1
Sweeney, K.J.2
Hamilton, J.A.3
-
6
-
-
0033926203
-
INK4a gene expression and methylation in primary breast cancer: overexpression of p16INK4a messenger RNA is a marker of poor prognosis
-
COI: 1:CAS:528:DC%2BD3cXlslentLs%3D, PID: 10914724
-
Hui R, Macmillan RD, Kenny FS, et al. INK4a gene expression and methylation in primary breast cancer: overexpression of p16INK4a messenger RNA is a marker of poor prognosis. Clin Cancer Res. 2000;6:2777–87.
-
(2000)
Clin Cancer Res
, vol.6
, pp. 2777-2787
-
-
Hui, R.1
Macmillan, R.D.2
Kenny, F.S.3
-
7
-
-
76049104235
-
PD 0332991, a selective cyclin D kinase 4/6 inhibitor, preferentially inhibits proliferation of luminal estrogen receptor-positive human breast cancer cell lines in vitro
-
PID: 19874578, Preclinical evidence supports preferential activity of palbociclib in luminal (hormone receptor positive) subtype breast cancer, as well as describes synergistic interactions when palbociclib is combined with tamoxifen and trastuzumab
-
Finn RS, Dering J, Conklin D, et al. PD 0332991, a selective cyclin D kinase 4/6 inhibitor, preferentially inhibits proliferation of luminal estrogen receptor-positive human breast cancer cell lines in vitro. Breast Cancer Res: BCR. 2009;11:R77. Preclinical evidence supports preferential activity of palbociclib in luminal (hormone receptor positive) subtype breast cancer, as well as describes synergistic interactions when palbociclib is combined with tamoxifen and trastuzumab.
-
(2009)
Breast Cancer Res: BCR
, vol.11
, pp. 77
-
-
Finn, R.S.1
Dering, J.2
Conklin, D.3
-
8
-
-
0028786916
-
Antiestrogen inhibition of cell cycle progression in breast cancer cells in associated with inhibition of cyclin-dependent kinase activity and decreased retinoblastoma protein phosphorylation
-
COI: 1:CAS:528:DyaK2MXhtVSjtLvE, PID: 8614416
-
Watts CK, Brady A, Sarcevic B, et al. Antiestrogen inhibition of cell cycle progression in breast cancer cells in associated with inhibition of cyclin-dependent kinase activity and decreased retinoblastoma protein phosphorylation. Mol Endocrinol. 1995;9:1804–13.
-
(1995)
Mol Endocrinol
, vol.9
, pp. 1804-1813
-
-
Watts, C.K.1
Brady, A.2
Sarcevic, B.3
-
9
-
-
79960100823
-
Therapeutically activating RB: reestablishing cell cycle control in endocrine therapy-resistant breast cancer
-
COI: 1:CAS:528:DC%2BC3MXpslKmsLs%3D, PID: 21367843
-
Thangavel C, Dean JL, Ertel A, et al. Therapeutically activating RB: reestablishing cell cycle control in endocrine therapy-resistant breast cancer. Endocrine-Related Cancer. 2011;18:333–45.
-
(2011)
Endocrine-Related Cancer
, vol.18
, pp. 333-345
-
-
Thangavel, C.1
Dean, J.L.2
Ertel, A.3
-
10
-
-
0030968438
-
CDK-independent activation of estrogen receptor by cyclin D1
-
COI: 1:CAS:528:DyaK2sXhtFagtbw%3D, PID: 9039267
-
Zwijsen RM, Wientjens E, Klompmaker R, et al. CDK-independent activation of estrogen receptor by cyclin D1. Cell. 1997;88:405–15.
-
(1997)
Cell
, vol.88
, pp. 405-415
-
-
Zwijsen, R.M.1
Wientjens, E.2
Klompmaker, R.3
-
11
-
-
3042536038
-
Preclinical and clinical development of the cyclin-dependent kinase inhibitor flavopiridol
-
COI: 1:CAS:528:DC%2BD2cXltFWls7o%3D, PID: 15217973
-
Shapiro GI. Preclinical and clinical development of the cyclin-dependent kinase inhibitor flavopiridol. Clin Cancer Res. 2004;10:4270s–5s.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 4270-4275
-
-
Shapiro, G.I.1
-
12
-
-
84878252263
-
Cyclin-dependent kinase inhibitor therapy for hematologic malignancies
-
COI: 1:CAS:528:DC%2BC3sXot1elu70%3D, PID: 23647051
-
Bose P, Simmons GL, Grant S. Cyclin-dependent kinase inhibitor therapy for hematologic malignancies. Expert Opin Investig Drugs. 2013;22:723–38.
-
(2013)
Expert Opin Investig Drugs
, vol.22
, pp. 723-738
-
-
Bose, P.1
Simmons, G.L.2
Grant, S.3
-
13
-
-
84906063822
-
Dinaciclib for the treatment of breast cancer
-
COI: 1:CAS:528:DC%2BC2cXhtlansr3N, PID: 25107301
-
Criscitiello C, Viale G, Esposito A, et al. Dinaciclib for the treatment of breast cancer. Expert Opin Investig Drugs. 2014;23:1305–12.
-
(2014)
Expert Opin Investig Drugs
, vol.23
, pp. 1305-1312
-
-
Criscitiello, C.1
Viale, G.2
Esposito, A.3
-
14
-
-
79952710710
-
Expression of p16 and retinoblastoma determines response to CDK4/6 inhibition in ovarian cancer
-
COI: 1:CAS:528:DC%2BC3MXjtFChtrc%3D
-
Konecny GE, Winterhoff B, Kolarova T, et al. Expression of p16 and retinoblastoma determines response to CDK4/6 inhibition in ovarian cancer. Clin Cancer Res: Off J Am Assoc Cancer Res. 2011;17:1591–602.
-
(2011)
Clin Cancer Res: Off J Am Assoc Cancer Res
, vol.17
, pp. 1591-1602
-
-
Konecny, G.E.1
Winterhoff, B.2
Kolarova, T.3
-
15
-
-
9444228344
-
Specific inhibition of cyclin-dependent kinase 4/6 by PD 0332991 and associated antitumor activity in human tumor xenografts
-
COI: 1:CAS:528:DC%2BD2cXpslCkt7c%3D, PID: 15542782
-
Fry DW, Harvey PJ, Keller PR, et al. Specific inhibition of cyclin-dependent kinase 4/6 by PD 0332991 and associated antitumor activity in human tumor xenografts. Mol Cancer Ther. 2004;3:1427–38.
-
(2004)
Mol Cancer Ther
, vol.3
, pp. 1427-1438
-
-
Fry, D.W.1
Harvey, P.J.2
Keller, P.R.3
-
16
-
-
84862877673
-
p16-Cdk4-Rb axis controls sensitivity to a cyclin-dependent kinase inhibitor PD0332991 in glioblastoma xenograft cells
-
COI: 1:CAS:528:DC%2BC38Xhtl2iu7%2FJ, PID: 22711607
-
Cen L, Carlson BL, Schroeder MA, et al. p16-Cdk4-Rb axis controls sensitivity to a cyclin-dependent kinase inhibitor PD0332991 in glioblastoma xenograft cells. Neuro-Oncology. 2012;14:870–81.
-
(2012)
Neuro-Oncology
, vol.14
, pp. 870-881
-
-
Cen, L.1
Carlson, B.L.2
Schroeder, M.A.3
-
17
-
-
84861210266
-
Selective CDK4/6 inhibition with tumor responses by PD0332991 in patients with mantle cell lymphoma
-
COI: 1:CAS:528:DC%2BC38XnsVKhtbY%3D, PID: 22383795
-
Leonard JP, LaCasce AS, Smith MR, et al. Selective CDK4/6 inhibition with tumor responses by PD0332991 in patients with mantle cell lymphoma. Blood. 2012;119:4597–607.
-
(2012)
Blood
, vol.119
, pp. 4597-4607
-
-
Leonard, J.P.1
LaCasce, A.S.2
Smith, M.R.3
-
18
-
-
79958149971
-
Phase I study of PD 0332991, a cyclin-dependent kinase inhibitor, administered in 3-week cycles (Schedule 2/1)
-
COI: 1:CAS:528:DC%2BC3MXntV2hsLc%3D, PID: 21610706
-
Schwartz GK, LoRusso PM, Dickson MA, et al. Phase I study of PD 0332991, a cyclin-dependent kinase inhibitor, administered in 3-week cycles (Schedule 2/1). Br J Cancer. 2011;104:1862–8.
-
(2011)
Br J Cancer
, vol.104
, pp. 1862-1868
-
-
Schwartz, G.K.1
LoRusso, P.M.2
Dickson, M.A.3
-
19
-
-
84855983664
-
Phase I, dose-escalation trial of the oral cyclin-dependent kinase 4/6 inhibitor PD 0332991, administered using a 21-day schedule in patients with advanced cancer
-
COI: 1:CAS:528:DC%2BC38XhtVGqs7o%3D
-
Flaherty KT, Lorusso PM, Demichele A, et al. Phase I, dose-escalation trial of the oral cyclin-dependent kinase 4/6 inhibitor PD 0332991, administered using a 21-day schedule in patients with advanced cancer. Clin Cancer Res:Off J Am Assoc Cancer Res. 2012;18:568–76.
-
(2012)
Clin Cancer Res:Off J Am Assoc Cancer Res
, vol.18
, pp. 568-576
-
-
Flaherty, K.T.1
Lorusso, P.M.2
Demichele, A.3
-
20
-
-
80054733690
-
Phase I study of PD 0332991, cyclin-D kinase (CDK) 4/6 inhibitor in combination with letrozole for first-line treatment of patients with ER-positive, HER2-negative breast cancer
-
Slamon DJ, Hurvitz SA, Applebaum S, et al. Phase I study of PD 0332991, cyclin-D kinase (CDK) 4/6 inhibitor in combination with letrozole for first-line treatment of patients with ER-positive, HER2-negative breast cancer. J Clin Oncol. 2010;15s:A3060.
-
(2010)
J Clin Oncol
, vol.15s
, pp. 3060
-
-
Slamon, D.J.1
Hurvitz, S.A.2
Applebaum, S.3
-
21
-
-
84923818100
-
A phase I trial of palbociclib and paclitaxel in metastatic breast cancer
-
Clark AS, O'Dwyer PJ, Heitjan D, et al. A phase I trial of palbociclib and paclitaxel in metastatic breast cancer. ASCO Meeting Abstracts. 2014;5s:A527.
-
(2014)
ASCO Meeting Abstracts
, vol.5s
, pp. 527
-
-
Clark, A.S.1
O'Dwyer, P.J.2
Heitjan, D.3
-
22
-
-
84864378859
-
CDK4/6 inhibition antagonizes the cytotoxic response to anthracycline therapy
-
COI: 1:CAS:528:DC%2BC38Xht1Oks7zL, PID: 22751436
-
McClendon AK, Dean JL, Rivadeneira DB, et al. CDK4/6 inhibition antagonizes the cytotoxic response to anthracycline therapy. Cell Cycle. 2012;11:2747–55.
-
(2012)
Cell Cycle
, vol.11
, pp. 2747-2755
-
-
McClendon, A.K.1
Dean, J.L.2
Rivadeneira, D.B.3
-
24
-
-
84923788537
-
-
Finn RS, Crown JP, Lang I, et al. The cyclin-dependent kinase 4/6 inhibitor palbociclib in combination with letrozole versus letrozole alone as first-line treatment of oestrogen receptor-positive, HER2-negative, advanced breast cancer (PALOMA-1/TRIO-18): a randomised phase 2 study. Lancet Oncol. 2014. The PALOMA 1 randomized phase 2 trial established the activity of the CDK 4/6 inhibitor palbociclib, described the toxicity profile in metastatic disease, and suggested superiority over standard first-line therapy with aromatase inhibitor
-
Finn RS, Crown JP, Lang I, et al. The cyclin-dependent kinase 4/6 inhibitor palbociclib in combination with letrozole versus letrozole alone as first-line treatment of oestrogen receptor-positive, HER2-negative, advanced breast cancer (PALOMA-1/TRIO-18): a randomised phase 2 study. Lancet Oncol. 2014. The PALOMA 1 randomized phase 2 trial established the activity of the CDK 4/6 inhibitor palbociclib, described the toxicity profile in metastatic disease, and suggested superiority over standard first-line therapy with aromatase inhibitor.
-
-
-
-
25
-
-
84930696140
-
Preclinical characterization of the CDK4/6 inhibitor LY2835219: in-vivo cell cycle-dependent/independent anti-tumor activities alone/in combination with gemcitabine
-
COI: 1:CAS:528:DC%2BC2cXhtVWrt7%2FN, PID: 24919854
-
Gelbert LM, Cai S, Lin X, et al. Preclinical characterization of the CDK4/6 inhibitor LY2835219: in-vivo cell cycle-dependent/independent anti-tumor activities alone/in combination with gemcitabine. Invest New Drugs. 2014;32:825–37.
-
(2014)
Invest New Drugs
, vol.32
, pp. 825-837
-
-
Gelbert, L.M.1
Cai, S.2
Lin, X.3
-
26
-
-
84904402837
-
Semi-mechanistic pharmacokinetic/pharmacodynamic modeling of the antitumor activity of LY2835219, a new cyclin-dependent kinase 4/6 inhibitor, in mice bearing human tumor xenografts
-
COI: 1:CAS:528:DC%2BC2cXhtFKlsrzE, PID: 24850847
-
Tate SC, Cai S, Ajamie RT, et al. Semi-mechanistic pharmacokinetic/pharmacodynamic modeling of the antitumor activity of LY2835219, a new cyclin-dependent kinase 4/6 inhibitor, in mice bearing human tumor xenografts. Clin Cancer Res. 2014;20:3763–74.
-
(2014)
Clin Cancer Res
, vol.20
, pp. 3763-3774
-
-
Tate, S.C.1
Cai, S.2
Ajamie, R.T.3
-
27
-
-
84903842102
-
LY2835219, a potent oral inhibitor of the cyclin-dependent kinases 4 and 6 (CDK4/6) that crosses the blood-brain barrier and demonstrates in vivo activity against intracranial human brain tumor xenografts
-
Abemaciclib, a CDK 4/6 inhibitor, has a differentiated activity and tolerability profile in comparison to palbociclib, and in particular, the potential ability to cross the blood brain barrier
-
Sanchez-Martinez C, Gelbert L, Shannon H, et al. LY2835219, a potent oral inhibitor of the cyclin-dependent kinases 4 and 6 (CDK4/6) that crosses the blood-brain barrier and demonstrates in vivo activity against intracranial human brain tumor xenografts. Mol Cancer Ther. 2011;10:B234. Abemaciclib, a CDK 4/6 inhibitor, has a differentiated activity and tolerability profile in comparison to palbociclib, and in particular, the potential ability to cross the blood brain barrier.
-
(2011)
Mol Cancer Ther
, vol.10
, pp. 234
-
-
Sanchez-Martinez, C.1
Gelbert, L.2
Shannon, H.3
-
28
-
-
84923794403
-
LY2835219, a novel cell cycle inhibitor selective for CDK4/6, in combination with fulvestrant for patients with hormone receptor positive (HR+) metastatic breast cancer
-
Patnaik A, Rosen L, Tolaney S, et al. LY2835219, a novel cell cycle inhibitor selective for CDK4/6, in combination with fulvestrant for patients with hormone receptor positive (HR+) metastatic breast cancer. J Clin Oncol. 2014;325s:A534.
-
(2014)
J Clin Oncol
, vol.325s
, pp. 534
-
-
Patnaik, A.1
Rosen, L.2
Tolaney, S.3
-
29
-
-
84905669286
-
A phase I study of the single-agent CDK4/6 inhibitor LEE011 in pts with advanced solid tumors and lymphomas
-
Infante JR, Shapiro G, Witteveen P, et al. A phase I study of the single-agent CDK4/6 inhibitor LEE011 in pts with advanced solid tumors and lymphomas. J Clin Oncol. 2014;5s:A2528.
-
(2014)
J Clin Oncol
, vol.5s
, pp. 2528
-
-
Infante, J.R.1
Shapiro, G.2
Witteveen, P.3
-
30
-
-
84904259645
-
CDK 4/6 inhibitors sensitize PIK3CA mutant breast cancer to PI3K inhibitors
-
COI: 1:CAS:528:DC%2BC2cXhtFans7rE, PID: 25002028, A complex relationship exists between PI3 kinase, Rb, and CDK 4/6. This preclinical experience suggests the combination of targeted biologics: a PI3K inhibitor and a CDK 4/6 inhibitor, is active and can overcome aspects of tumor resistance to therapy
-
Vora SR, Juric D, Kim N, et al. CDK 4/6 inhibitors sensitize PIK3CA mutant breast cancer to PI3K inhibitors. Cancer Cell. 2014;26:136–49. A complex relationship exists between PI3 kinase, Rb, and CDK 4/6. This preclinical experience suggests the combination of targeted biologics: a PI3K inhibitor and a CDK 4/6 inhibitor, is active and can overcome aspects of tumor resistance to therapy.
-
(2014)
Cancer Cell
, vol.26
, pp. 136-149
-
-
Vora, S.R.1
Juric, D.2
Kim, N.3
-
32
-
-
84886438147
-
The cell-cycle regulator CDK4: an emerging therapeutic target in melanoma
-
COI: 1:CAS:528:DC%2BC3sXhsFyns7bO, PID: 24089445
-
Sheppard KE, McArthur GA. The cell-cycle regulator CDK4: an emerging therapeutic target in melanoma. Clin Cancer Res. 2013;19:5320–8.
-
(2013)
Clin Cancer Res
, vol.19
, pp. 5320-5328
-
-
Sheppard, K.E.1
McArthur, G.A.2
|