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Imbalanced expression pattern of steroid receptor coactivator-1 and -3 in liver cancer compared with normal liver: An
Shan Li1,2, Huiyan Zhang3, Yanlan Yu1,2
1Department of Neurobiology, Chongqing Key Laboratory of Neurobiology, Third Military Medical University, Chongqing 400038, P.R. China.
Abstract:
Steroids affect normal and pathological functions of the liver through receptors, which require coactivators for their transcriptional activation. Steroid receptor coactivator (SRC)-1 and SRC-3 have been demonstrated to be regulated in numerous cancers; however, their expression profiles in liver cancer including hepatocellular carcinoma (HCC) and cholangiocellular carcinoma (CCC) remain unclear. Using tissue microarray immunohistochemistry, normal liver tissue and HCC tissue exhibited immunoreactivity of SRC-1, which were predominantly localized within extranuclear components; in CCC, they were detected within the cell nuclei; SRC-3 was also detected in the cell nuclei. Furthermore, no altered expression of SRC-1 and SRC-3 was observed in liver cancer compared with normal liver tissue; however, in CCC, the expression of SRC-3 was significantly increased compared with that detected in HCC. Importantly, although expression of SRC-1 and SRC-3 did not reveal any significant differences (30 vs. 40%) in normal liver tissue, HCC and CCC expression of SRC-1 was significantly decreased compared with that of SRC-3 (9.3 vs. 36%, and 6.7 vs. 67.7% for HCC and CCC, respectively). Further comparative analysis revealed that this discrepancy was detected in males with liver cancer, across all ages of HCC cases, younger CCC cases and all stages of liver cancer. The results suggested the presence of an imbalanced expression pattern of SRC-1 and SRC-3 from normal liver tissue to liver cancer (decreased SRC-1 and increased SRC-3), which may affect hepatic function and therefore promote liver carcinogenesis.
Insights
Steroid receptor coactivator (SRC)-1 and SRC-3 expression is altered in liver cancer. SRC-1 decreases while SRC-3 increases, potentially promoting liver carcinogenesis.
Area of Science:
- Hepatology
- Oncology
- Molecular Biology
Background:
- Steroids regulate liver function via receptors needing coactivators.
- Steroid receptor coactivator (SRC)-1 and SRC-3 are implicated in various cancers.
- SRC-1 and SRC-3 expression in liver cancer (HCC, CCC) is not well understood.
Purpose of the Study:
- To investigate SRC-1 and SRC-3 expression profiles in normal liver tissue, hepatocellular carcinoma (HCC), and cholangiocellular carcinoma (CCC).
- To determine the role of SRC-1 and SRC-3 expression patterns in liver carcinogenesis.
Main Methods:
- Tissue microarray immunohistochemistry was used to analyze SRC-1 and SRC-3 expression.
- Immunoreactivity and localization of SRC-1 and SRC-3 were examined in normal liver, HCC, and CCC tissues.
Main Results:
- SRC-1 and SRC-3 were detected in normal liver, HCC, and CCC tissues, with varying subcellular localizations.
- While overall SRC-1 and SRC-3 expression didn't significantly differ between normal liver and cancer, CCC showed increased SRC-3 compared to HCC.
- SRC-1 expression significantly decreased relative to SRC-3 in both HCC and CCC, a pattern observed across different patient demographics and cancer stages.
Conclusions:
- Liver cancer exhibits an imbalanced SRC-1 and SRC-3 expression pattern (decreased SRC-1, increased SRC-3) compared to normal liver tissue.
- This imbalanced expression may disrupt hepatic function and contribute to liver carcinogenesis.
- Further research into the specific roles of SRC-1 and SRC-3 in liver cancer pathogenesis is warranted.
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