Accession Number : ADA464063


Title :   ErbB4 Overexpression as an Antagonist of ErbB2/HER2/Neu Induced Human Breast Cancer Cell Proliferation


Descriptive Note : Annual summary 1 Aug 2003-31 Jul 2006


Corporate Author : TULANE UNIV NEW ORLEANS LA


Personal Author(s) : Long, Weiwen ; Duplessis, Tamika


Full Text : https://apps.dtic.mil/dtic/tr/fulltext/u2/a464063.pdf


Report Date : Aug 2006


Pagination or Media Count : 24


Abstract : To test the hypothesis that ERBB4 signaling suppresses ERBB2-mediated cell proliferation in breast cancer, we introduced ERBB4 into SKBR-3 and MCF-7 breast cancer cell lines, which overexpress and express normal levels of ErbB2, respectively. We found that ERBB4 induces apoptosis in over 40% of both SKBR-3 and MCF-7 cells. Significantly, the normal human mammary epithelial cell line hTERT-HME was resistant to ERBB4 induced apoptosis. Although ERBB4 apoptotic function requires kinase activity, neither MAPK nor Pl3-K signaling is involved in ERBB4 induced apoptosis. Further studies indicate that ERBB4 couples to the intrinsic apoptotic pathway through the mitochondrial proapoptotic protein Bak. A search for proapoptotic domains in ERBB4 revealed a putative BH3 domain within ERBB4 intracellular domain (410D). We found that 4lCD exhibits equivalent level of apoptotic activity as holoreceptor of ERBB4 and, in contrast, does not require the kinase activity. These findings suggest that ERBB4 kinase activity contributes to apoptosis by generating 4lCD from the cell membrane upon proteolytic cleavage. Mutation of the BH3 domain of 4lCD significantly decreases 4lCD-induced apoptosis. Taken together, our data indicate that ERBB4 functions as a proapoptotic BH3-only protein. The specificity of ERBB4 cell- killing for malignant cells further supports a tumor suppressor function for ERBB4.


Descriptors :   *BREAST CANCER , FUNCTIONS , MEMBRANES(BIOLOGY) , PROTEINS , NEOPLASMS , HYPOTHESES , CELLS(BIOLOGY) , PHARMACOLOGICAL ANTAGONISTS , CANCER , SUPPRESSORS , PEPTIDE HYDROLASES , PHOSPHORUS TRANSFERASES


Subject Categories : Anatomy and Physiology
      Medicine and Medical Research


Distribution Statement : APPROVED FOR PUBLIC RELEASE