Exploiting selective BCL-2 family inhibitors to dissect cell survival dependencies and define improved strategies for cancer therapy

Author:

Leverson Joel D.1,Phillips Darren C.1,Mitten Michael J.1,Boghaert Erwin R.1,Diaz Dolores2,Tahir Stephen K.1,Belmont Lisa D.2,Nimmer Paul1,Xiao Yu1,Ma Xiaoju Max2,Lowes Kym N.34,Kovar Peter1,Chen Jun1,Jin Sha1,Smith Morey1,Xue John1,Zhang Haichao1,Oleksijew Anatol1,Magoc Terrance J.1,Vaidya Kedar S.1,Albert Daniel H.1,Tarrant Jacqueline M.2,La Nghi2,Wang Le1,Tao Zhi-Fu1,Wendt Michael D.1,Sampath Deepak2,Rosenberg Saul H.1,Tse Chris1,S. Huang David C.34,Fairbrother Wayne J.2,Elmore Steven W.1,Souers Andrew J.1

Affiliation:

1. AbbVie Inc., North Chicago, IL 60064, USA.

2. Genentech Inc., South San Francisco, CA 94080, USA.

3. Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia.

4. Department of Medical Biology, University of Melbourne, Parkville, Victoria 3010, Australia.

Abstract

Selective inhibition of BCL-X L synergizes with docetaxel to inhibit the growth of solid tumors but does not inhibit granulopoiesis.

Funder

Leukemia and Lymphoma Society

Medical Research Council

Australian Cancer Research Foundation

Cancer Council Victoria

Australian National Health

Independent Research Institutes Infrastructure Support Scheme

Victorian State Government Operational Infrastructure Support

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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