Thyroid hormone suppresses expression of stathmin and associated tumor growth in hepatocellular carcinoma

Yi Hsin Tseng, Ya Hui Huang, Tzu Kang Lin, Sheng Ming Wu, Hsiang Cheng Chi, Chung Ying Tsai, Ming Chieh Tsai, Yang Hsiang Lin, Wei Chun Chang, Ya Ting Chang, Wei Jan Chen, Kwang Huei Lin

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18 Citations (Scopus)


Stathmin (STMN1), a recognized oncoprotein upregulated in various solid tumors, promotes microtubule disassembly and modulates tumor growth and migration activity. However, the mechanisms underlying the genetic regulation of STMN1 have yet to be elucidated. In the current study, we report that thyroid hormone receptor (THR) expression is negatively correlated with STMN1 expression in a subset of clinical hepatocellular carcinoma (HCC) specimens. We further identified the STMN1 gene as a target of thyroid hormone (T 3) in the HepG2 hepatoma cell line. An analysis of STMN1 expression profile and mechanism of transcriptional regulation revealed that T 3 significantly suppressed STMN1 mRNA and protein expression, and further showed that THR directly targeted the STMN1 upstream element to regulate STMN1 transcriptional activity. Specific knockdown of STMN1 suppressed cell proliferation and xenograft tumor growth in mice. In addition, T 3 regulation of cell growth arrest and cell cycle distribution were attenuated by overexpression of STMN1. Our results suggest that the oncogene STMN1 is transcriptionally downregulated by T 3 in the liver. This T 3-mediated suppression of STMN1 supports the theory that T 3 plays an inhibitory role in HCC tumor growth, and suggests that the lack of normal THR function leads to elevated STMN1 expression and malignant growth.

Original languageEnglish
Article number38756
JournalScientific Reports
Publication statusPublished - Dec 9 2016
Externally publishedYes

ASJC Scopus subject areas

  • General


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