Identification and Characterization of a Small Molecule Bcl-2 Functional Converter

Author:

Kopparapu Prasad R.1ORCID,Pearce Martin C.1ORCID,Löhr Christiane V.2ORCID,Duong Cathy1ORCID,Jang Hyo Sang1ORCID,Tyavanagimatt Shanthakumar1ORCID,O'Donnell Edmond F.1ORCID,Nakshatri Harikrishna3ORCID,Kolluri Siva K.14ORCID

Affiliation:

1. 1Cancer Research Laboratory, Department of Environmental and Molecular Toxicology, Oregon State University, Corvallis, Oregon.

2. 2Department of Biomedical Sciences, Carlson College of Veterinary Medicine, Oregon State University, Corvallis, Oregon.

3. 3Department of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.

4. 4Linus Pauling Institute, Oregon State University, Corvallis, Oregon.

Abstract

Abstract Cancer cells exploit the expression of anti-apoptotic protein Bcl-2 to evade apoptosis and develop resistance to therapeutics. High levels of Bcl-2 leads to sequestration of pro-apoptotic proteins causing the apoptotic machinery to halt. In this study, we report discovery of a small molecule, BFC1108 (5-chloro-N-(2-ethoxyphenyl)-2-[(4-methoxybenzyol)amino]benzamide), which targets Bcl-2 and converts it into a pro-apoptotic protein. The apoptotic effect of BFC1108 is not inhibited, but rather potentiated, by Bcl-2 overexpression. BFC1108 induces a conformational change in Bcl-2, resulting in the exposure of its BH3 domain both in vitro and in vivo. BFC1108 suppresses the growth of triple-negative breast cancer xenografts with high Bcl-2 expression and inhibits breast cancer lung metastasis. This study demonstrates a novel approach to targeting Bcl-2 using BFC1108, a small molecule Bcl-2 functional converter that effectively induces apoptosis in Bcl-2–expressing cancers. Significance: We report the identification of a small molecule that exposes the Bcl-2 killer conformation and induces death in Bcl-2–expressing cancer cells. Selective targeting of Bcl-2 and elimination of cancer cells expressing Bcl-2 opens up new therapeutic avenues.

Funder

HHS | NIH | National Cancer Institute

DOD | USA | MEDCOM | Congressionally Directed Medical Research Programs

U.S. Department of Agriculture

Publisher

American Association for Cancer Research (AACR)

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