| Literature DB >> 29695515 |
Mary K McKenna1,2, Sunil K Noothi1,2,3, Sara S Alhakeem1,2, Karine Z Oben1,2, Joseph T Greene4,5, Rajeswaran Mani4,5, Kathryn L Perry1, James P Collard1,2, Jacqueline R Rivas1,2, Gerhard C Hildebrandt2,6, Roger A Fleischman2,6, Eric B Durbin2, John C Byrd4,5, Chi Wang2, Natarajan Muthusamy4,5, Vivek M Rangnekar1,2,3, Subbarao Bondada1,2.
Abstract
Prostate apoptosis response-4 (Par-4), a proapoptotic tumor suppressor protein, is downregulated in many cancers including renal cell carcinoma, glioblastoma, endometrial, and breast cancer. Par-4 induces apoptosis selectively in various types of cancer cells but not normal cells. We found that chronic lymphocytic leukemia (CLL) cells from human patients and from Eµ-Tcl1 mice constitutively express Par-4 in greater amounts than normal B-1 or B-2 cells. Interestingly, knockdown of Par-4 in human CLL-derived Mec-1 cells results in a robust increase in p21/WAF1 expression and decreased growth due to delayed G1-to-S cell-cycle transition. Lack of Par-4 also increased the expression of p21 and delayed CLL growth in Eμ-Tcl1 mice. Par-4 expression in CLL cells required constitutively active B-cell receptor (BCR) signaling, as inhibition of BCR signaling with US Food and Drug Administration (FDA)-approved drugs caused a decrease in Par-4 messenger RNA and protein, and an increase in apoptosis. In particular, activities of Lyn, a Src family kinase, spleen tyrosine kinase, and Bruton tyrosine kinase are required for Par-4 expression in CLL cells, suggesting a novel regulation of Par-4 through BCR signaling. Together, these results suggest that Par-4 may play a novel progrowth rather than proapoptotic role in CLL and could be targeted to enhance the therapeutic effects of BCR-signaling inhibitors.Entities:
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Year: 2018 PMID: 29695515 PMCID: PMC6024641 DOI: 10.1182/blood-2017-10-813931
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113