Skip to main content
Log in

Upregulated HOXC8 Expression Is Associated with Poor Prognosis and Oxaliplatin Resistance in Hepatocellular Carcinoma

  • Original Article
  • Published:
Digestive Diseases and Sciences Aims and scope Submit manuscript

Abstract

Background

Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related deaths worldwide. It is indispensable to understanding molecular mechanisms of HCC progression and to developing clinically useful biomarkers for this disease.

Aim

In this article, we examined whether HOXC8 was associated with the poor prognosis of hepatocellular carcinoma and explored the possible underlying mechanism.

Methods

The HOXC8 and Ki67 expression levels in 86 patients with hepatocellular carcinoma were examined using immunohistochemistry. HOXC8 levels in HCC cells were downregulated by siRNA transfection. The cycle progression and cell proliferation status of HCC cells and the oxaliplatin effectiveness were evaluated by flow cytometry and CCK-8 assay. HOXC8, CyclinD1, PCNA, Nkd2, and cleaved caspase-3 levels were detected by western blot.

Results

HOXC8 was upregulated in HCC tissues, compared with adjacent non-tumor ones. HOXC8 expression levels in 86 patients with hepatocellular carcinoma were positively correlated with histological grade. Univariate and multivariate survival analysis revealed that HOXC8 was a significant predictor for overall survival of HCC patients. HOXC8 siRNA knockdown delayed the G1–S phase transition, inhibited cell proliferation, and attenuated resistance to oxaliplatin.

Conclusions

HOXC8 promoted HCC proliferation and predicted poor prognosis. Furthermore, upregulated HOXC8 expression was associated with oxaliplatin resistance in hepatocellular carcinoma.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  1. Morozov TK, Potekhina VA. Characteristics of performing a periodic medical examination in the transition to annual dispensary care for workers. Gigiena i sanitariia. 1986;2:28–30.

    PubMed  Google Scholar 

  2. Schafer DF, Sorrell MF. Hepatocellular carcinoma. Lancet. 1999;353:1253–1257.

    Article  CAS  PubMed  Google Scholar 

  3. Cao H, Phan H, Yang LX. Improved chemotherapy for hepatocellular carcinoma. Anticancer Res. 2012;32:1379–1386.

    CAS  PubMed  Google Scholar 

  4. Montero J, Morales A, Llacuna L, et al. Mitochondrial cholesterol contributes to chemotherapy resistance in hepatocellular carcinoma. Cancer Res. 2008;68:5246–5256.

    Article  CAS  PubMed  Google Scholar 

  5. Asghar U, Meyer T. Are there opportunities for chemotherapy in the treatment of hepatocellular cancer? J Hepatol. 2012;56:686–695.

    Article  PubMed  Google Scholar 

  6. Du H, Yang W, Chen L, et al. Role of autophagy in resistance to oxaliplatin in hepatocellular carcinoma cells. Oncol Rep. 2012;27:143–150.

    CAS  PubMed  Google Scholar 

  7. Gehring WJ, Hiromi Y. Homeotic genes and the homeobox. Annu Rev Genet. 1986;20:147–173.

    Article  CAS  PubMed  Google Scholar 

  8. Pearson JC, Lemons D, McGinnis W. Modulating Hox gene functions during animal body patterning. Nat Rev Genet. 2005;6:893–904.

    Article  CAS  PubMed  Google Scholar 

  9. Mann RS, Morata G. The developmental and molecular biology of genes that subdivide the body of Drosophila. Annu Rev Cell Dev Biol. 2000;16:243–271.

    Article  CAS  PubMed  Google Scholar 

  10. McGinnis W, Krumlauf R. Homeobox genes and axial patterning. Cell. 1992;68:283–302.

    Article  CAS  PubMed  Google Scholar 

  11. Tiret L, Le Mouellic H, Maury M, Brulet P. Increased apoptosis of motoneurons and altered somatotopic maps in the brachial spinal cord of Hoxc-8-deficient mice. Development. 1998;125:279–291.

    CAS  PubMed  Google Scholar 

  12. Kamel S, Kruger C, Salbaum JM, Kappen C. Morpholino-mediated knockdown in primary chondrocytes implicates Hoxc8 in regulation of cell cycle progression. Bone. 2009;44:708–716.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  13. Yang X, Ji X, Shi X, Cao X. Smad1 domains interacting with Hoxc-8 induce osteoblast differentiation. J Biol Chem. 2000;275:1065–1072.

    Article  CAS  PubMed  Google Scholar 

  14. Min H, Lee JY, Bok J, Chung HJ, Kim MH. Proliferating cell nuclear antigen (Pcna) as a direct downstream target gene of Hoxc8. Biochem Biophys Res Commun. 2010;392:543–547.

    Article  CAS  PubMed  Google Scholar 

  15. Miller GJ, Miller HL, van Bokhoven A, et al. Aberrant HOXC expression accompanies the malignant phenotype in human prostate. Cancer Res. 2003;63:5879–5888.

    CAS  PubMed  Google Scholar 

  16. Alami Y, Castronovo V, Belotti D, Flagiello D, Clausse N. HOXC5 and HOXC8 expression are selectively turned on in human cervical cancer cells compared to normal keratinocytes. Biochem Biophys Res Commun. 1999;257:738–745.

    Article  CAS  PubMed  Google Scholar 

  17. Waltregny D, Alami Y, Clausse N, de Leval J, Castronovo V. Overexpression of the homeobox gene HOXC8 in human prostate cancer correlates with loss of tumor differentiation. Prostate. 2002;50:162–169.

    Article  CAS  PubMed  Google Scholar 

  18. Axlund SD, Lambert JR, Nordeen SK. HOXC8 inhibits androgen receptor signaling in human prostate cancer cells by inhibiting SRC-3 recruitment to direct androgen target genes. Mol Cancer Res MCR. 2010;8:1643–1655.

    Article  CAS  PubMed  Google Scholar 

  19. Li Y, Guo Z, Chen H, et al. HOXC8-dependent cadherin 11 expression facilitates breast cancer cell migration through Trio and Rac. Genes Cancer. 2011;2:880–888.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  20. Li Y, Zhang M, Chen H, et al. Ratio of miR-196s to HOXC8 messenger RNA correlates with breast cancer cell migration and metastasis. Cancer Res. 2010;70:7894–7904.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  21. Wan C, Hou S, Ni R, et al. MIF4G domain containing protein regulates cell cycle and hepatic carcinogenesis by antagonizing CDK2-dependent p27 stability. Oncogene. 2015;34:237–245.

    Article  CAS  PubMed  Google Scholar 

  22. Lei H, Juan AH, Kim MS, Ruddle FH. Mouse naked cuticle 2 (mNkd2) as a direct transcriptional target of Hoxc8 in vivo. J Exp Zool Part A Ecol Genet Physiol. 2007;307:1–6.

    Article  Google Scholar 

  23. Zhang S, Cagatay T, Amanai M, et al. Viable mice with compound mutations in the Wnt/Dvl pathway antagonists nkd1 and nkd2. Mol Cell Biol. 2007;27:4454–4464.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  24. Rousset R, Mack JA, Wharton KA Jr, et al. Naked cuticle targets dishevelled to antagonize Wnt signal transduction. Genes Dev. 2001;15:658–671.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  25. Yuzugullu H, Benhaj K, Ozturk N, et al. Canonical Wnt signaling is antagonized by noncanonical Wnt5a in hepatocellular carcinoma cells. Mol Cancer. 2009;8:90.

    Article  PubMed Central  PubMed  Google Scholar 

  26. Katoh M. Molecular cloning, gene structure, and expression analyses of NKD1 and NKD2. Int J Oncol. 2001;19:963–969.

    CAS  PubMed  Google Scholar 

  27. Prasad CP, Gupta SD, Rath G, Ralhan R. Wnt signaling pathway in invasive ductal carcinoma of the breast: relationship between beta-catenin, dishevelled and cyclin D1 expression. Oncology. 2007;73:112–117.

    Article  CAS  PubMed  Google Scholar 

  28. Ohhara Y, Suenaga M, Matsusaka S, Shinozaki E, Mizunuma N, Yamaguchi T. Comparison between three oxaliplatin-based regimens with bevacizumab in patients with metastatic colorectal cancer. OncoTargets Ther. 2015;8:529–537.

    Article  Google Scholar 

  29. Wu P, Zhu X, Jin W, Hao S, Liu Q, Zhang L. Oxaliplatin triggers necrosis as well as apoptosis in gastric cancer SGC-7901 cells. Biochem Biophys Res Commun. 2015;460:183–190.

    Article  CAS  PubMed  Google Scholar 

  30. Wang XH, Meng XW, Sun X, Du YJ, Zhao J, Fan YJ. Wnt/b-catenin signaling pathway affects the protein expressions of caspase-3, XIAP and Grp-78 in hepatocellular carcinoma. Zhonghua gan zang bing za zhi= Zhonghua ganzangbing zazhi= Chinese Journal of Hepatology. 2011;19:599–602.

    CAS  PubMed  Google Scholar 

  31. Pang RW, Poon RT. From molecular biology to targeted therapies for hepatocellular carcinoma: the future is now. Oncology. 2007;72:30–44.

    Article  CAS  PubMed  Google Scholar 

  32. Lee TK, Man K, Ho JW, et al. Significance of the Rac signaling pathway in HCC cell motility: implications for a new therapeutic target. Carcinogenesis. 2005;26:681–687.

    Article  CAS  PubMed  Google Scholar 

  33. Ma WL, Hsu CL, Wu MH et al. Androgen receptor is a new potential therapeutic target for the treatment of hepatocellular carcinoma. Gastroenterology. 2008;135:947–955, 955 e941–945.

  34. Calvo R, West J, Franklin W, et al. Altered HOX and WNT7A expression in human lung cancer. Proc Natl Acad Sci USA. 2000;97:12776–12781.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  35. Ferrell CM, Dorsam ST, Ohta H, et al. Activation of stem-cell specific genes by HOXA9 and HOXA10 homeodomain proteins in CD34+ human cord blood cells. Stem Cells. 2005;23:644–655.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

This study was supported by the National Natural Science Foundation of China (Nos. 81472272, 81472708).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Buyou Chen.

Ethics declarations

Conflict of interest

None.

Additional information

Pan Xu and Xiubing Zhang contributed equally to this work.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Xu, P., Zhang, X., Ni, W. et al. Upregulated HOXC8 Expression Is Associated with Poor Prognosis and Oxaliplatin Resistance in Hepatocellular Carcinoma. Dig Dis Sci 60, 3351–3363 (2015). https://doi.org/10.1007/s10620-015-3774-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10620-015-3774-x

Keywords

Navigation