| Literature DB >> 33042443 |
Zachary M Connelly1, Renjie Jin2, Jianghong Zhang2, Shu Yang1, Siyuan Cheng1, Mingxia Shi3, Justin Mm Cates4, Runhua Shi5, David J DeGraff6, Peter S Nelson7, Yunlong Liu8, Colm Morrissey9, Eva Corey9, Xiuping Yu1,10.
Abstract
Bone metastasis frequently occurs in advanced-stage prostate cancer (PCa) patients. Understanding the mechanisms that promote PCa-mediated bone destruction is important for the identification of therapeutic targets against this lethal disease. We found that forkhead box A2 (FOXA2) is expressed in a subset of PCa bone metastasis specimens. To determine the functional role of FOXA2 in PCa metastasis, we knocked down the expression of FOXA2 in PCa PC3 cells, which can grow in bones and elicit an osteolytic reaction. The PC3/FOXA2-knockdown cells generated fewer bone lesions following intra-tibial injection compared to control cells. Further, we found that FOXA2 knockdown decreased the expression of PTHLH, which encodes PTHrP, a well-established factor that regulates bone remodeling. These results indicate that FOXA2 is involved in PCa bone metastasis. AJTREntities:
Keywords: FOXA2; PTHrP; bone; prostate cancer
Year: 2020 PMID: 33042443 PMCID: PMC7540102
Source DB: PubMed Journal: Am J Transl Res ISSN: 1943-8141 Impact factor: 4.060