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      Ethnic differences in TGFβ-signaling pathway may contribute to prostate cancer health disparity

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          Abstract

          Epidemiological studies show that the incidence and mortality rates of prostate cancer (PCa) are significantly higher in African-American (AA) men when compared with Caucasian (CA) men in the United States. Transforming growth factor β (TGFβ) signaling pathway is linked to health disparities in AAs. Recent studies suggest a role of TGFβ3 in cancer metastases and its effect on the migratory and invasive behavior; however, its role in PCa in AA men has not been studied. We determined the circulating levels of TGFβ3 in AA and CA men diagnosed with PCa using ELISA. We analyzed serum samples from both AA and CA men diagnosed with and without PCa. We show that AA PCa patients had higher levels of TGFβ3 protein compared with AA controls and CA patients. In fact, TGFβ3 protein levels in serum were higher in AA men without PCa compared with the CA population, which may correlate with more aggressive disease seen in AA men. Studies on AA-derived PCa cell lines revealed that TGFβ3 protein levels were also higher in these cells compared with CA-derived PCa cell lines. Our studies also reveal that TGFβ does not inhibit cell proliferation in AA-derived PCa cell lines, but it does induce migration and invasion through activation of PI3K pathway. We suggest that increased TGFβ3 levels are responsible for development of aggressive PCa in AA patients as a consequence of development of resistance to inhibitory effects of TGFβ on cell proliferation and induction of invasive metastatic behavior.

          Abstract

          Circulating levels of TGFβ3 are much higher in AA PCa patients compared with those in CA patients. AA-derived PCa cell lines also express high levels of TGFβ3 and exert significant stimulatory effects on cell migration and invasion.

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          Author and article information

          Journal
          Carcinogenesis
          Carcinogenesis
          carcin
          Carcinogenesis
          Oxford University Press (UK )
          0143-3334
          1460-2180
          April 2018
          21 February 2018
          05 April 2019
          : 39
          : 4
          : 546-555
          Affiliations
          [1 ]Center for Cancer Research and Therapeutic Development, Atlanta, GA, USA
          [2 ]Department of Mathematical Sciences, Clark Atlanta University, Atlanta, GA, USA
          [3 ]Fox Chase Cancer Center-Temple Health, Philadelphia, PA, USA
          Author notes
          To whom correspondence should be addressed. Tel: +1 404 880 6795; Fax: +1 404 880 6756; Email: skhan@ 123456cau.edu
          Article
          PMC5889036 PMC5889036 5889036 bgy020
          10.1093/carcin/bgy020
          5889036
          29474521
          2fcd1aa7-1568-4781-9cc3-adbf88abde9b
          © The Author(s) 2018. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

          This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model ( https://academic.oup.com/journals/pages/about_us/legal/notices)

          History
          : 12 September 2017
          : 12 December 2017
          : 02 February 2018
          Page count
          Pages: 10
          Funding
          Funded by: National Institutes of Health 10.13039/100000002
          Award ID: G12MD007590
          Award ID: 5P20MD002285
          Categories
          Biology, Genetics and Epigenetics

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