Department of Biochemistry, University of Illinois, Urbana, Illinios, IL 61801, USA

Correspondence to: Z Huang, Department of Biochemistry, University of Illinois, Urbana, Illinios, IL 61801, USA

Bcl-2 family proteins are key regulators of programmed cell death or apoptosis that is implicated in many human diseases, particularly cancer. In recent years, they have attracted intensive interest in both basic research to understand the fundamental principles of cell survival and cell death and drug discovery to develop a new class of anticancer agents. The Bcl-2 family includes both anti- and pro-apoptotic proteins with opposing biological functions in either inhibiting or promoting cell death. High expression of anti-apoptotic members such as Bcl-2 and Bcl-x_L commonly found in human cancers contributes to neoplastic cell expansion and interferes with the therapeutic action of many chemotherapeutic drugs. The functional blockade of Bcl-2 or Bcl-x_L could either restore the apoptotic process in tumor cells or sensitize these tumors for chemo- and radiotherapies. This article reviews the recent progress in the design and discovery of small molecules that block the anti-apoptotic function of Bcl-2 or Bcl-x_L. These chemical inhibitors are effective modulators of apoptosis and promising leads for the further development of new anticancer agents. Oncogene (2000) 19, 6627-6631.

Bcl-2; apoptosis; caspase; cancer; chemoresistance; drug design