Literature DB >> 26306734

New directions for drug-resistant breast cancer: the CDK4/6 inhibitors.

Mark Nichols1.   

Abstract

Many breast cancers are treated with selective estrogen receptor modulators (SERMs) if the cancers are estrogen and progesterone hormone receptor positive. However, some 30% are not responsive or later become resistant to such therapies. There has been continued interest in developing new and more effective SERMs that target the estrogen receptors for therapeutic benefit. This article will focus on therapies directed against other molecular targets to improve outcomes, as preventing growth of breast cancer cells by an unrelated mechanism is most likely to yield success against resistance, or synergize in a combination therapy with SERMs or aromatase inhibitors. New drugs in development that target the cyclin-dependent kinases CDK4/CDK6 have 'breakthrough therapy' designation at the US FDA and may provide an exciting and realistic new avenue to patients in the near future.

Entities:  

Mesh:

Substances:

Year:  2015        PMID: 26306734      PMCID: PMC4625900          DOI: 10.4155/fmc.15.86

Source DB:  PubMed          Journal:  Future Med Chem        ISSN: 1756-8919            Impact factor:   3.808


  14 in total

1.  Third-generation SERMs may face uphill battle.

Authors:  Charlie Schmidt
Journal:  J Natl Cancer Inst       Date:  2010-11-08       Impact factor: 13.506

2.  CDK inhibitors in cancer therapy: what is next?

Authors:  Marcos Malumbres; Paolo Pevarello; Mariano Barbacid; James R Bischoff
Journal:  Trends Pharmacol Sci       Date:  2007-12-04       Impact factor: 14.819

3.  Requirement for CDK4 kinase function in breast cancer.

Authors:  Qunyan Yu; Ewa Sicinska; Yan Geng; Marie Ahnström; Agnieszka Zagozdzon; Yinxin Kong; Humphrey Gardner; Hiroaki Kiyokawa; Lyndsay N Harris; Olle Stål; Piotr Sicinski
Journal:  Cancer Cell       Date:  2006-01       Impact factor: 31.743

Review 4.  Understanding the role of thyroid hormone in Sertoli cell development: a mechanistic hypothesis.

Authors:  Denise R Holsberger; Paul S Cooke
Journal:  Cell Tissue Res       Date:  2005-11-03       Impact factor: 5.249

5.  Dual CDK4/CDK6 inhibition induces cell-cycle arrest and senescence in neuroblastoma.

Authors:  Julieann Rader; Mike R Russell; Lori S Hart; Michael S Nakazawa; Lili T Belcastro; Daniel Martinez; Yimei Li; Erica L Carpenter; Edward F Attiyeh; Sharon J Diskin; Sunkyu Kim; Sudha Parasuraman; Giordano Caponigro; Robert W Schnepp; Andrew C Wood; Bruce Pawel; Kristina A Cole; John M Maris
Journal:  Clin Cancer Res       Date:  2013-09-17       Impact factor: 12.531

6.  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.

Authors:  Richard S Finn; Judy Dering; Dylan Conklin; Ondrej Kalous; David J Cohen; Amrita J Desai; Charles Ginther; Mohammad Atefi; Isan Chen; Camilla Fowst; Gerret Los; Dennis J Slamon
Journal:  Breast Cancer Res       Date:  2009       Impact factor: 6.466

Review 7.  Update on raloxifene: role in reducing the risk of invasive breast cancer in postmenopausal women.

Authors:  Victor G Vogel
Journal:  Breast Cancer (Dove Med Press)       Date:  2011-10-20

8.  PD-0332991, a potent and selective inhibitor of cyclin-dependent kinase 4/6, demonstrates inhibition of proliferation in renal cell carcinoma at nanomolar concentrations and molecular markers predict for sensitivity.

Authors:  Joshua E Logan; Nikayeh Mostofizadeh; Amrita J Desai; Erika VON Euw; Dylan Conklin; Veerauo Konkankit; Habib Hamidi; Mark Eckardt; Lee Anderson; Hsiao-Wang Chen; Charles Ginther; Eileen Taschereau; Peter H Bui; James G Christensen; Arie S Belldegrun; Dennis J Slamon; Fairooz F Kabbinavar
Journal:  Anticancer Res       Date:  2013-08       Impact factor: 2.480

Review 9.  Use of SERMs for treatment in postmenopausal women.

Authors:  Joann V Pinkerton; Semara Thomas
Journal:  J Steroid Biochem Mol Biol       Date:  2013-12-25       Impact factor: 4.292

10.  Combination anastrozole and fulvestrant in metastatic breast cancer.

Authors:  Rita S Mehta; William E Barlow; Kathy S Albain; Ted A Vandenberg; Shaker R Dakhil; Nagendra R Tirumali; Danika L Lew; Daniel F Hayes; Julie R Gralow; Robert B Livingston; Gabriel N Hortobagyi
Journal:  N Engl J Med       Date:  2012-08-02       Impact factor: 91.245

View more
  3 in total

1.  Dopamine D2 receptor antagonist sulpiride enhances dexamethasone responses in the treatment of drug-resistant and metastatic breast cancer.

Authors:  Jian Li; Qing-Yu Yao; Jun-Sheng Xue; Li-Jie Wang; Yin Yuan; Xiu-Yun Tian; Hong Su; Si-Yuan Wang; Wen-Jun Chen; Wei Lu; Tian-Yan Zhou
Journal:  Acta Pharmacol Sin       Date:  2017-06-26       Impact factor: 6.150

2.  Ganoderiol F purified from Ganoderma leucocontextum retards cell cycle progression by inhibiting CDK4/CDK6.

Authors:  Xiangmin Li; Yizhen Xie; Juanjuan Peng; Huiping Hu; Qingping Wu; Burton B Yang
Journal:  Cell Cycle       Date:  2019-09-22       Impact factor: 4.534

Review 3.  Breakthroughs in modern cancer therapy and elusive cardiotoxicity: Critical research-practice gaps, challenges, and insights.

Authors:  Ping-Pin Zheng; Jin Li; Johan M Kros
Journal:  Med Res Rev       Date:  2017-09-01       Impact factor: 12.944

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.