메뉴 건너뛰기




Volumn 22, Issue 6, 2015, Pages e498-e501

Does CDKN2A loss predict palbociclib benefit?

Author keywords

Breast cancer; Medical oncology

Indexed keywords

ALPHA TOCOPHEROL; ANASTROZOLE; CAPECITABINE; CYCLIN DEPENDENT KINASE INHIBITOR 2A; EPIDERMAL GROWTH FACTOR RECEPTOR 2; FULVESTRANT; GAMMA UROGASTRONE; LETROZOLE; PALBOCICLIB; PENTOXIFYLLINE; PROGESTERONE RECEPTOR;

EID: 84951806875     PISSN: None     EISSN: 17187729     Source Type: Journal    
DOI: 10.3747/co.22.2700     Document Type: Article
Times cited : (16)

References (13)
  • 1
    • 84922369296 scopus 로고    scopus 로고
    • 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 randomized phase 2 study
    • 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 randomized phase 2 study. Lancet Oncol 2015;16:25-35.
    • (2015) Lancet Oncol , vol.16 , pp. 25-35
    • Finn, R.S.1    Crown, J.P.2    Lang, I.3
  • 2
    • 84937042338 scopus 로고    scopus 로고
    • Palbociclib in hormone-receptor- positive advanced breast cancer
    • Turner NC, Ro J, Andre F, et al. Palbociclib in hormone-receptor- positive advanced breast cancer. N Engl J Med 2015;373:209-19.
    • (2015) N Engl J Med , vol.373 , pp. 209-219
    • Turner, N.C.1    Ro, J.2    Andre, F.3
  • 3
    • 77954997865 scopus 로고    scopus 로고
    • Mitigation of hematologic radiation toxicity in mice through pharmacological quiescence induced by cdk4/6 inhibition
    • Johnson SM, Torrice CD, Bell JF, et al. Mitigation of hematologic radiation toxicity in mice through pharmacological quiescence induced by cdk4/6 inhibition. J Clin Invest 2010;120:2528-36.
    • (2010) J Clin Invest , vol.120 , pp. 2528-2536
    • Johnson, S.M.1    Torrice, C.D.2    Bell, J.F.3
  • 4
    • 30344470210 scopus 로고    scopus 로고
    • Requirement for cdk4 kinase function in breast cancer
    • Yu Q, Sicinska E, Geng Y, et al. Requirement for cdk4 kinase function in breast cancer. Cancer Cell 2006;9:23-32.
    • (2006) Cancer Cell , vol.9 , pp. 23-32
    • Yu, Q.1    Sicinska, E.2    Geng, Y.3
  • 5
    • 84920591660 scopus 로고    scopus 로고
    • cdk6 as a key regulator of hematopoietic and leukemic stem cell activation
    • Scheicher R, Hoelbl-Kovacic A, Bellutti F, et al. cdk6 as a key regulator of hematopoietic and leukemic stem cell activation. Blood 2015;125:90-101.
    • (2015) Blood , vol.125 , pp. 90-101
    • Scheicher, R.1    Hoelbl-Kovacic, A.2    Bellutti, F.3
  • 6
    • 84951805439 scopus 로고    scopus 로고
    • Molecular features that determine the sensitivity of cancer cells to abemaciclib, an inhibitor of cdk4 and cdk6 [abstract 3104]
    • Gong X, Chiou LC, Lallena M, et al. Molecular features that determine the sensitivity of cancer cells to abemaciclib, an inhibitor of cdk4 and cdk6 [abstract 3104]. Cancer Res 2015;75:3104.
    • (2015) Cancer Res , vol.75 , pp. 3104
    • Gong, X.1    Chiou, L.C.2    Lallena, M.3
  • 7
    • 84951754985 scopus 로고    scopus 로고
    • Clinical activity of LY2835219, a novel cell cycle inhibitor selective for cdk4 and cdk6, in patients with metastatic breast cancer [abstract CT232]
    • Patnaik A, Rosen LS, Tolaney SM, et al. Clinical activity of LY2835219, a novel cell cycle inhibitor selective for cdk4 and cdk6, in patients with metastatic breast cancer [abstract CT232]. Cancer Res 2014;74:.
    • (2014) Cancer Res , vol.74
    • Patnaik, A.1    Rosen, L.S.2    Tolaney, S.M.3
  • 8
    • 84888082787 scopus 로고    scopus 로고
    • Dual cdk4/cdk6 inhibition induces cell-cycle arrest and senescence in neuroblastoma
    • Rader J, Russell MR, Hart LS, et al. Dual cdk4/cdk6 inhibition induces cell-cycle arrest and senescence in neuroblastoma. Clin Cancer Res 2013;19:6173-82.
    • (2013) Clin Cancer Res , vol.19 , pp. 6173-6182
    • Rader, J.1    Russell, M.R.2    Hart, L.S.3
  • 9
    • 84885416415 scopus 로고    scopus 로고
    • p16 and p53 play distinct roles in different subtypes of breast cancer
    • Shan M, Zhang X, Liu X, et al. p16 and p53 play distinct roles in different subtypes of breast cancer. PLoS One 2013;8:e76408.
    • (2013) PLoS One , vol.8
    • Shan, M.1    Zhang, X.2    Liu, X.3
  • 10
    • 84874091851 scopus 로고    scopus 로고
    • Methylation and immunoexpression of p16(INK4a) tumor suppressor gene in primary breast cancer tissue and their quantitative p16(INK4a) hypermethylation in plasma by real-time pcr
    • Lee JJ, Ko E, Cho J, et al. Methylation and immunoexpression of p16(INK4a) tumor suppressor gene in primary breast cancer tissue and their quantitative p16(INK4a) hypermethylation in plasma by real-time pcr. Korean J Pathol 2012;46:554-61.
    • (2012) Korean J Pathol , vol.46 , pp. 554-561
    • Lee, J.J.1    Ko, E.2    Cho, J.3
  • 11
    • 84893748029 scopus 로고    scopus 로고
    • p16 but not retinoblastoma expression is related to clinical outcome in no-special-type triple-negative breast carcinomas
    • Bogina GS, Lunardi G, Marcolini L et al. p16 but not retinoblastoma expression is related to clinical outcome in no-special-type triple-negative breast carcinomas. Mod Pathol 2014;27:204-13.
    • (2014) Mod Pathol , vol.27 , pp. 204-213
    • Bogina, G.S.1    Lunardi, G.2    Marcolini, L.3
  • 13
    • 76049104235 scopus 로고    scopus 로고
    • PD0332991, a selective cycl in D kinase 4/6 inhibitor, preferent ial ly inhibits proliferation of luminal estrogen receptor-positive human breast cancer cell lines in vitro
    • Finn R, Dering J, Conklin D, et al. PD0332991, a selective cycl in D kinase 4/6 inhibitor, preferent ial ly inhibits proliferation of luminal estrogen receptor-positive human breast cancer cell lines in vitro. Breast Cancer Res 2009;11:R77.
    • (2009) Breast Cancer Res , vol.11
    • Finn, R.1    Dering, J.2    Conklin, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.