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PKM2‐regulated STAT3 promotes esophageal squamous cell carcinoma progression via TGF‐β1‐induced EMT
Author(s) -
Ma Rong,
Liu Qing,
Zheng Shutao,
Liu Tao,
Tan Doudou,
Lu Xiaomei
Publication year - 2019
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.28434
Subject(s) - cancer research , pkm2 , cell migration , epithelial–mesenchymal transition , gene knockdown , downregulation and upregulation , small hairpin rna , biology , vimentin , cell growth , metastasis , gene silencing , transforming growth factor , cell , cancer , microbiology and biotechnology , cell culture , immunology , pyruvate kinase , immunohistochemistry , endocrinology , glycolysis , biochemistry , genetics , metabolism , gene
Recent studies have demonstrated pleiotropic roles of pyruvate kinase isoenzyme type M2 (PKM2) in tumor progression. However, the precise mechanisms underlying the effects of PKM2 on esophageal squamous cell carcinoma (ESCC) metastasis and transforming growth factor β1 (TGF‐β1)‐induced epithelial‐mesenchymal transition (EMT) remain to be established. In this study, we observed upregulation of PKM2 in ESCC tissues that was markedly associated with lymph node metastasis and poor prognosis. High PKM2 expression in tumor tissues frequently coincided with the high pSTAT3Tyr705 expression and low E‐cadherin expression. Furthermore, altered PKM2 expression was significantly associated with proliferation, migration, and invasion of ESCC cells, in addition to expression patterns of EMT markers (Snail, E‐cadherin, and vimentin) and pSTAT3 Tyr705 /STAT3 ratio. Overexpression of STAT3 significantly attenuated the effects of PKM2 knockdown on cell proliferation and motility as well as expression of pSTAT3 Tyr705 and EMT markers. Consistently, stable short hairpin RNA (shRNA)‐mediated silencing of PKM2 reversed the effects of TGF‐β1 treatment, specifically, upregulation of PKM2, phosphorylation of STAT3 at Tyr705, and increased EMT, migration, and invasion. We propose that PKM2 regulates cell proliferation, migration, and invasion via phosphorylation of STAT3 through TGF‐β1‐induced EMT. Our findings collectively provide mechanistic insights into the tumor‐promoting role of PKM2, supporting its prognostic value and the therapeutic utility of PKM2 inhibitors as potential antitumor agents in ESCC.