Literature DB >> 27573352

TSC22D2 interacts with PKM2 and inhibits cell growth in colorectal cancer.

Fang Liang1, Qiao Li1, Xiayu Li2, Zheng Li1, Zhaojian Gong3, Hao Deng2, Bo Xiang1, Ming Zhou1, Xiaoling Li1, Guiyuan Li1, Zhaoyang Zeng1, Wei Xiong1.   

Abstract

We previously identified TSC22D2 (transforming growth factor β-stimulated clone 22 domain family, member 2) as a novel cancer-associated gene in a rare multi-cancer family. However, its role in tumor development remains completely unknown. In this study, we found that TSC22D2 was significantly downregulated in colorectal cancer (CRC) and that TSC22D2 overexpression inhibited cell growth. Using a co-immunoprecipitation (co-IP) assay combined with mass spectrometry analysis to identify TSC22D2-interacting proteins, we demonstrated that TSC22D2 interacts with pyruvate kinase isoform M2 (PKM2). These findings were confirmed by the results of immunoprecipitation and immunofluorescence assays. Moreover, overexpression of TSC22D2 reduced the level of nuclear PKM2 and suppressed cyclin D1 expression. Collectively, our study reveals a growth suppressor function of TSC22D2 that is at least partially dependent on the TSC22D2-PKM2-cyclinD1 regulatory axis. In addition, our data provide important clues that might contribute to future studies evaluating the role of TSC22D2.

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Year:  2016        PMID: 27573352     DOI: 10.3892/ijo.2016.3599

Source DB:  PubMed          Journal:  Int J Oncol        ISSN: 1019-6439            Impact factor:   5.650


  23 in total

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5.  BPIFB1 (LPLUNC1) inhibits migration and invasion of nasopharyngeal carcinoma by interacting with VTN and VIM.

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Review 7.  Role of long non-coding RNAs in glucose metabolism in cancer.

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Review 8.  Linking long non-coding RNAs and SWI/SNF complexes to chromatin remodeling in cancer.

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Review 9.  LncRNAs regulate cancer metastasis via binding to functional proteins.

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Review 10.  The role of exosomal non-coding RNAs in cancer metastasis.

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Journal:  Oncotarget       Date:  2017-12-21
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