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Fem1b, a proapoptotic protein, mediates proteasome inhibitor‐induced apoptosis of human colon cancer cells
Author(s) -
Subauste M. Cecilia,
Sansom Owen J.,
Porecha Nehal,
Raich Natacha,
Du Liqin,
Maher Joseph F.
Publication year - 2010
Publication title -
molecular carcinogenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.254
H-Index - 97
eISSN - 1098-2744
pISSN - 0899-1987
DOI - 10.1002/mc.20594
Subject(s) - biology , proteasome inhibitor , apoptosis , downregulation and upregulation , cancer research , inhibitor of apoptosis , proteasome , cancer , cancer cell , transfection , microbiology and biotechnology , programmed cell death , cell culture , gene , biochemistry , genetics
In the treatment of colon cancer, the development of resistance to apoptosis is a major factor in resistance to therapy. New molecular approaches to overcome apoptosis resistance, such as selectively upregulating proapoptotic proteins, are needed in colon cancer therapy. In a mouse model with inactivation of the adenomatous polyposis coli ( Apc ) tumor suppressor gene, reflecting the pathogenesis of most human colon cancers, the gene encoding feminization‐1 homolog b (Fem1b) is upregulated in intestinal epithelium following Apc inactivation. Fem1b is a proapoptotic protein that interacts with apoptosis‐inducing proteins Fas, tumor necrosis factor receptor‐1 (TNFR1), and apoptotic protease activating factor‐1 (Apaf‐1). Increasing Fem1b expression induces apoptosis of cancer cells, but effects on colon cancer cells have not been reported. Fem1b is a homolog of feminization‐1 (FEM‐1), a protein in Caenorhabditis elegans that is regulated by proteasomal degradation, but whether Fem1b is likewise regulated by proteasomal degradation is unknown. Herein, we found that Fem1b protein is expressed in primary human colon cancer specimens, and in malignant SW620, HCT‐116, and DLD‐1 colon cancer cells. Increasing Fem1b expression, by transfection of a Fem1b expression construct, induced apoptosis of these cells. We found that proteasome inhibitor treatment of SW620, HCT‐116, and DLD‐1 cells caused upregulation of Fem1b protein levels, associated with induction of apoptosis. Blockade of Fem1b upregulation with morpholino antisense oligonucleotide suppressed the proteasome inhibitor‐induced apoptosis of these cells. In conclusion, the proapoptotic protein Fem1b is downregulated by the proteasome in malignant colon cancer cells and mediates proteasome inhibitor‐induced apoptosis of these cells. Therefore, Fem1b could represent a novel molecular target to overcome apoptosis resistance in therapy of colon cancer. © 2009 Wiley‐Liss, Inc.