Alternative splicing of estrogen receptor alpha in hepatocellular carcinoma.

BMC Cancer

Department of Surgery, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, New Territories, Hong Kong, Special Administrative Region of China.

Published: November 2016

AI Article Synopsis

  • The study investigates the roles of estrogen receptor alpha (ERa), estrogen receptor beta (ERb), and a variant called ERa36 in hepatocellular carcinoma (HCC) using three patient cohorts.
  • It finds that in primary HCC, WtERa levels are downregulated while ERa36 levels are upregulated, contrasting with secondary HCC where ERa36 is downregulated.
  • The research suggests that these expression patterns of ERa36 may help differentiate between primary and secondary HCC types, with implications for patient prognosis and treatment strategies.

Article Abstract

Background: The role of estrogen receptor alpha (ERa), estrogen receptor beta (ERb) and ERa36 signaling in hepatocellular carcinoma (HCC) is not fully addressed.

Methods: In this study, three cohorts were included: (i) primary HCC patients (N = 76, cohort P), (ii) colorectal liver metastasis (mCRC) (N = 32, cohort S), and (iii) HCC from The Cancer Genome Atlas (TCGA) (N = 121). The levels of ERa36 and wtER36 were measured and their correlation with clinicopathologic features was determined.

Results: WtERa was downregulated and that ERa36 was upregulated in tumor tissues in both cohort P and TCGA data set. ERa36 was downregulated in tumor tissues in cohort S. In cohort P, wtERa was differentially expressed in gender (P < 0.000), age (P = 0.004), tumor number (P = 0.043), tumor size (P = 0.002), intrahepatic recurrence (P = 0.054). ERa36 was unequally expressed in different non-tumor liver status (P = 0.040). WtERa was negatively associated with overall survival (OS) and disease free survival (DFS) in cohort P. Compared with non-tumor tissues, the expression of ERa36 was increased in primary HCC but decreased in secondary HCC, showing opposite expression patterns of ERa36 between primary HCC and secondary HCC.

Conclusions: Primary HCC is associated with the decreased WtERa but increased ERa36. The expression pattern of ERa36 is different between primary HCC and secondary HCC, as the former with the increased ERa36 but the latter with the decreased ERa36. Therefore, the expression of ERa36 may be used to differentiate the primary HCC and the secondary one.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129602PMC
http://dx.doi.org/10.1186/s12885-016-2928-3DOI Listing

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