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Expression and prognostic value of Ars2 in hepatocellular carcinoma

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Abstract

Background

Hepatocellular carcinoma (HCC) is one of the most common malignant tumors in China. Arsenic resistance protein 2 (Asr2) was reported to be important for microRNA (miR) biogenesis, and its depletion could reduce the levels of several miRs, including miR-21, which is over-expressed in HCC. We hypothesized that Ars2 is also overexpressed in HCC and may be involved in the biological properties of HCC.

Methods

Ars2 immunolabeling was evaluated in 132 HCCs. Ars2 immunolabeling, Ars2 qRT-PCR and miR-21 were evaluated in 20 HCCs and in paired normal tissues. Ars2 shRNA was transfected into SMCC-7721 and HepG2 HCC cells. The cell proliferation and expression of Ars2 and miR-21 were subsequently evaluated.

Results

Ars2 was expressed primarily in the nucleus of HCC cells. The expression of Ars2 was statistically correlated with the loss of HCC differentiation and pathological stage. The survival rates of patients with low Ars2 expression in HCC were statistically higher than patients with overexpressed Ars2 in HCC. Ars2 and miR-21 were more highly expressed in HCC specimens than normal tissues, and they were also correlated. The knockdown of Ars2 in HCC cells inhibited miR-21 expression and cell proliferation.

Conclusions

Ars2 is overexpressed in HCC and may have prognostic value; it might play an important role in HCC proliferation and miR-21 expression.

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References

  1. Fares N, Peron JM (2013) Epidemiology, natural history, and risk factors of hepatocellular carcinoma. La Revue du praticien 63:216–217, 220–212

    Google Scholar 

  2. Tang ZY (2001) Hepatocellular carcinoma: cause, treatment and metastasis. World J Gastroenterol 7:445–454

    PubMed  CAS  Google Scholar 

  3. Deshmukh M, Hoshida Y (2013) Genomic profiling of cell lines for personalized targeted therapy for hepatocellular carcinoma. Hepatology. doi:10.1002/hep.26407

    PubMed  PubMed Central  Google Scholar 

  4. Gruber JJ, Zatechka DS, Sabin LR et al (2009) Ars2 links the nuclear cap-binding complex to RNA interference and cell proliferation. Cell 138:328–339

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  5. Sabin LR, Zhou R, Gruber JJ et al (2009) Ars2 regulates both miRNA- and siRNA- dependent silencing and suppresses RNA virus infection in Drosophila. Cell 138:340–351

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  6. Beezhold KJ, Castranova V, Chen F (2010) Microprocessor of microRNAs: regulation and potential for therapeutic intervention. Mol Cancer 9:134

    Article  PubMed  PubMed Central  Google Scholar 

  7. Gramantieri L, Fornari F, Callegari E et al (2008) MicroRNA involvement in hepatocellular carcinoma. J Cell Mol Med 12:2189–2204

    Article  PubMed  CAS  Google Scholar 

  8. You N, Liu W, Wang T et al (2012) Swainsonine inhibits growth and potentiates the cytotoxic effect of paclitaxel in hepatocellular carcinoma in vitro and in vivo. Oncol Rep 28:2091–2100

    PubMed  CAS  Google Scholar 

  9. Matuo MC, de Oliveira Takamoto RT, Kikuchi IS et al (2013) Effect of bixin and norbixin on the expression of cytochrome P450 in HepG2 cell line. Cell Biol Int 37:843–848

    Article  PubMed  CAS  Google Scholar 

  10. He Q, Cai L, Shuai L et al (2013) Ars2 is overexpressed in human cholangiocarcinomas and its depletion increases PTEN and PDCD4 by decreasing microRNA-21. Mol Carcinog 52:286–296

    Article  PubMed  CAS  Google Scholar 

  11. Soman G, Yang X, Jiang H et al (2009) MTS dye based colorimetric CTLL-2 cell proliferation assay for product release and stability monitoring of interleukin-15: assay qualification, standardization and statistical analysis. J Immunol Methods 348:83–94

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  12. Andreu-Agullo C, Maurin T (2012) Ars2, an essential player in neural stem cell identity. Med Sci 28:459–462

    Google Scholar 

  13. Wilson MD, Wang D, Wagner R et al (2008) ARS2 is a conserved eukaryotic gene essential for early mammalian development. Mol Cell Biol 28:1503–1514

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  14. Bentwich I, Avniel A, Karov Y et al (2005) Identification of hundreds of conserved and nonconserved human microRNAs. Nat Genet 37:766–770

    Article  PubMed  CAS  Google Scholar 

  15. Lewis BP, Burge CB, Bartel DP (2005) Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets. Cell 120:15–20

    Article  PubMed  CAS  Google Scholar 

  16. Friedman RC, Farh KK, Burge CB et al (2009) Most mammalian mRNAs are conserved targets of microRNAs. Genome Res 19:92–105

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  17. Lim LP, Lau NC, Weinstein EG et al (2003) The microRNAs of Caenorhabditis elegans. Genes Dev 17:991–1008

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  18. Morrisey EE (2010) The magic and mystery of miR-21. J Clin Invest 120:3817–3819

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  19. Bhatti I, Lee A, James V et al (2011) Knockdown of microRNA-21 inhibits proliferation and increases cell death by targeting programmed cell death 4 (PDCD4) in pancreatic ductal adenocarcinoma. J Gastrointest Surg 15:199–208

    Article  PubMed  Google Scholar 

  20. Selaru FM, Olaru AV, Kan T et al (2009) MicroRNA-21 is overexpressed in human cholangiocarcinoma and regulates programmed cell death 4 and tissue inhibitor of metalloproteinase 3. Hepatology 49:1595–1601

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  21. Pezzolesi MG, Platzer P, Waite KA et al (2008) Differential expression of PTEN-targeting microRNAs miR-19a and miR-21 in Cowden syndrome. Am J Hum Genet 82:1141–1149

    Article  PubMed  CAS  PubMed Central  Google Scholar 

Download references

Acknowledgments

This work was partially supported by the National Science Foundation of China (NSFC) grants 81201948/H1617.

Conflict of interest

No author has any conflict of interest.

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Authors

Corresponding author

Correspondence to Chenghua Zhang.

Additional information

Q. He and Y. Huang contributed equally to this work.

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He, Q., Huang, Y., Cai, L. et al. Expression and prognostic value of Ars2 in hepatocellular carcinoma. Int J Clin Oncol 19, 880–888 (2014). https://doi.org/10.1007/s10147-013-0642-6

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  • DOI: https://doi.org/10.1007/s10147-013-0642-6

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