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TP53/miR-34a-associated signaling targets SERPINE1 expression in human pancreatic cancer
Author(s) -
Shaw M. Akula,
Peter P. Ruvolo,
James A. McCubrey
Publication year - 2020
Publication title -
aging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 90
ISSN - 1945-4589
DOI - 10.18632/aging.102776
Subject(s) - pancreatic cancer , cancer research , expression (computer science) , signal transduction , microrna , medicine , cancer , oncology , biology , microbiology and biotechnology , computer science , genetics , gene , programming language
Pancreatic ductal adenocarcinoma (PDAC) is a disease of aging. The TP53 gene product regulates cell growth, aging, and cancer. To determine the important targets of TP53 in PDAC, we examined the expression of 440 proteins on a reverse phase protein array (RPPA) in PDAC-derived MIA-PaCa-2 cells which either had WT- TP53 or lacked WT- TP53 . MIA-PaCa-2 cells have a TP53 mutation as well as mutant KRAS and represent a good in vitro model to study PDAC. RPPA analysis demonstrated expression of tumor promoting proteins in cells that lacked WT- TP53 ; and this feature could be reversed significantly when the cells were transfected with vector encoding WT- TP53 or treated with berberine or a modified berberine (BBR). Expression of miR-34a-associated signaling was elevated in cells expressing WT- TP53 compared to cells expressing mTP53 . Results from in vivo studies using human PDAC specimens confirmed the in vitro results as the expression of miR-34a and associated signaling was significantly decreased in PDAC specimens compared to non-cancerous tissues. This study determined SERPINE1 as a miR-34a target with relevance to the biology of PDAC. Thus, we have identified a key target ( SERPINE1 ) of the TP53/miR-34a axis that may serve as a potential biomarker for early detection of pancreatic cancer.

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