Cell permeable Bcl-2 binding peptides: a chemical approach to apoptosis induction in tumor cells

  • Cancer Res. 2000 Mar 15;60(6):1498-502.
J L Wang  1 ,  Z J Zhang ,  S Choksi ,  S Shan ,  Z Lu ,  C M Croce ,  E S Alnemri ,  R Korngold ,  Z Huang
Affiliations
  • 1. Kimmel Cancer Center, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
PMID: 10749111
Abstract

Bcl-2 is a potent suppressor of Apoptosis, and its overexpression contributes to tumorigenesis in many types of human cancers. To test the possibility of modulating Bcl-2 function as an Anticancer strategy, a cell permeable Bcl-2 binding peptide, cell permeable moiety (cpm)-1285, was designed by chemically attaching a fatty acid to a peptide derived from the proapoptotic protein Bad. cpm-1285 entered HL-60 tumor cells, bound Bcl-2 protein, and induced Apoptosis in vitro. In contrast, cpm-1285 had little effect on normal human peripheral blood lymphocytes. Furthermore, cpm-1285 had in vivo activity in slowing human myeloid leukemia growth in severe combined immunodeficient mice. These results demonstrate a novel approach for therapeutic intervention of tumor growth in vivo with small molecule inhibitors of Bcl-2.

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