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Clinical significance and biological roles of TRIM24 in human bladder carcinoma

  • Research Article
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Tumor Biology

Abstract

Tripartite motif-containing 24 (TRIM24), also known as transcription intermediary factor 1-alpha (TIF1α), is a chromatin-associated protein which as been has been implicated in carcinogenesis. However, its expression profile and biological roles in human bladder carcinoma has not been investigated. In this study, we examined its expression in 95 bladder cancer specimens. We found that TRIM24 expression was upregulated in 39 of 95 (41.1 %) specimens compared with normal control. TRIM24 overexpression was associated with local invasion and advanced grade of bladder cancer. In addition, we transfected TRIM24 plasmid into BIU-87 cell line and TRIM24 siRNA into 5637 cell line. Colony formation, CCK-8, and transwell assay were used to assess its biological roles in bladder cancer cells. The result showed that TRIM24 could facilitate cancer cell growth and invading ability. Western blot analysis demonstrated that TRIM24 upregulated cyclin D1, cyclin E, p-IκBα, and p-AKT expression, suggesting TRIM24 activates NF-κB and AKT pathways. In addition, NF-κB inhibitor reversed the effect of TRIM24 on cyclin D1. In conclusion, TRIM24 is overexpressed in human bladder cancer and facilitates bladder cancer growth and invasion, possibly through NF-κB and AKT signaling pathways.

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References

  1. Siegel R, Naishadham D, Jemal A. Cancer statistics, 2012. CA Cancer J Clin. 2012;62(1):10–29.

    Article  PubMed  Google Scholar 

  2. Meng XD et al. Increased SPHK1 expression is associated with poor prognosis in bladder cancer. Tumour Biol. 2014;35(3):2075–80.

    Article  CAS  PubMed  Google Scholar 

  3. Liu J et al. Clinical significance of UNC5B expression in bladder cancer. Tumour Biol. 2013;34(4):2099–108.

    Article  CAS  PubMed  Google Scholar 

  4. Le Douarin B et al. The N-terminal part of TIF1, a putative mediator of the ligand-dependent activation function (AF-2) of nuclear receptors, is fused to B-raf in the oncogenic protein T18. EMBO J. 1995;14(9):2020–33.

    PubMed  PubMed Central  Google Scholar 

  5. Le Douarin B et al. A possible involvement of TIF1 alpha and TIF1 beta in the epigenetic control of transcription by nuclear receptors. EMBO J. 1996;15(23):6701–15.

    PubMed  PubMed Central  Google Scholar 

  6. Le Douarin B et al. TIF1 alpha: a chromatin-specific mediator for the ligand-dependent activation function AF-2 of nuclear receptors? Biochem Soc Trans. 1997;25(2):605–12.

    Article  PubMed  Google Scholar 

  7. Tsai WW et al. TRIM24 links a non-canonical histone signature to breast cancer. Nature. 2010;468(7326):927–32.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Khetchoumian K et al. Loss of Trim24 (Tif1alpha) gene function confers oncogenic activity to retinoic acid receptor alpha. Nat Genet. 2007;39(12):1500–6.

    Article  CAS  PubMed  Google Scholar 

  9. Chambon M et al. Prognostic significance of TRIM24/TIF-1alpha gene expression in breast cancer. Am J Pathol. 2011;178(4):1461–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Li H et al. Overexpression of TRIM24 correlates with tumor progression in non-small cell lung cancer. PLoS One. 2012;7(5):e37657.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Cui Z et al. TRIM24 overexpression is common in locally advanced head and neck squamous cell carcinoma and correlates with aggressive malignant phenotypes. PLoS One. 2013;8(5):e63887.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Liu X et al. Overexpression of TRIM24 is associated with the onset and progress of human hepatocellular carcinoma. PLoS One. 2014;9(1):e85462.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Chambon M et al. Prognostic significance of TRIM24/TIF-1alpha gene expression in breast cancer. Am J Pathol. 2011;178(4):1461–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Zhang LH, et al. TRIM24 promotes glioma progression and enhances chemoresistance through activation of the PI3K/Akt signaling pathway. Oncogene. 2014.

  15. Tashiro E, Tsuchiya A, Imoto M. Functions of cyclin D1 as an oncogene and regulation of cyclin D1 expression. Cancer Sci. 2007;98(5):629–35.

    Article  CAS  PubMed  Google Scholar 

  16. Witzel II, Koh LF, Perkins ND. Regulation of cyclin D1 gene expression. Biochem Soc Trans. 2010;38(Pt 1):217–22.

    Article  CAS  PubMed  Google Scholar 

  17. Fristrup N et al. Multicenter validation of cyclin D1, MCM7, TRIM29, and UBE2C as prognostic protein markers in non-muscle-invasive bladder cancer. Am J Pathol. 2013;182(2):339–49.

    Article  CAS  PubMed  Google Scholar 

  18. Hennessy BT et al. Exploiting the PI3K/AKT pathway for cancer drug discovery. Nat Rev Drug Discov. 2005;4(12):988–1004.

    Article  CAS  PubMed  Google Scholar 

  19. Lu B et al. Tumor suppressor TSLC1 is implicated in cell proliferation, invasion and apoptosis in laryngeal squamous cell carcinoma by regulating Akt signaling pathway. Tumour Biol. 2012;33(6):2007–17.

    Article  CAS  PubMed  Google Scholar 

  20. Yu Y et al. AKT signaling pathway activated by HIN-1 methylation in non-small cell lung cancer. Tumour Biol. 2012;33(2):307–14.

    Article  CAS  PubMed  Google Scholar 

  21. Man X et al. Clinical significance and biological roles of CARMA3 in human bladder carcinoma. Tumour Biol. 2014;35(5):4131–6.

    Article  CAS  PubMed  Google Scholar 

  22. Tang ZP et al. Ataxia-telangiectasia group D complementing gene (ATDC) upregulates matrix metalloproteinase 9 (MMP-9) to promote lung cancer cell invasion by activating ERK and JNK pathways. Tumour Biol. 2013;34(5):2835–42.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

This work was supported by the grants from the Scientific Research Fund of Liaoning Provincial Education Department, China (No. L2014318).

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Correspondence to Ping Wang.

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Xue, D., Zhang, X., Zhang, X. et al. Clinical significance and biological roles of TRIM24 in human bladder carcinoma. Tumor Biol. 36, 6849–6855 (2015). https://doi.org/10.1007/s13277-015-3393-3

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  • DOI: https://doi.org/10.1007/s13277-015-3393-3

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