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microRNA-107 functions as a candidate tumor-suppressor gene in head and neck squamous cell carcinoma by downregulation of protein kinase Cɛ

Abstract

Head and neck squamous cell carcinoma (HNSCC) is the sixth most prevalent cancer worldwide with about 600 000 new cases diagnosed each year. Understanding the molecular pathways that lead to HNSCC is crucial to identify new targets for anti-cancer drug development. Protein kinase Cɛ (PKCɛ) is elevated in HNSCC and regulates the activation of Akt, Stat3 and Rho GTPases. To date, the molecular mechanism of PKCɛ dysregulation in HNSCC remains to be elucidated. In silico analysis identified three putative microRNA-107 (miR-107) binding sites in the 3′-untranslated region (UTR) of PKCɛ. An inverse relationship was revealed between miR-107 and PKCɛ in HNSCC cell lines. Delivery of miR-107 reduced PKCɛ levels in SCC15, SCC25 and CAL27, three HNSCC cell lines with high PKCɛ and low miR-107. The activity of a luciferase reporter construct containing the 3′-UTR of PKCɛ was downregulated by miR-107 and mutations in the three cognate miR-107 binding sites completely ablated the regulation by miR-107. Treatment with miR-107 significantly blocked cell proliferation, DNA replication, colony formation and invasion in SCC25 and CAL27 cells. Ectopic expression of miR-resistant PKCɛ was sufficient to partially rescue the loss-of-function phenotype in miR-107-overexpressing SCC25 cells. Tumor growth in nude mice was retarded by 93±7% in CAL27/miR-107 cells compared with CAL27/miR-control cells. Last, human primary HNSCC tumors with elevated PKCɛ had reduced miR-107 expression. Our results demonstrate that PKCɛ is directly regulated by miR-107 and, moreover, suggest that miR-107 may be a potential anti-cancer therapeutic for HNSCC.

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References

  • Avissar M, Christensen BC, Kelsey KT, Marsit CJ . (2009). MicroRNA expression ratio is predictive of head and neck squamous cell carcinoma. Clin Cancer Res 15: 2850–2855.

    Article  CAS  Google Scholar 

  • Ayala de la Pena F, Kanasaki K, Kanasaki M, Tangirala N, Maeda G, Kalluri R . (2011). Loss of p53 and acquisition of angiogenic microRNA profile is insufficient to facilitate progression of bladder urothelial carcinoma in situ to invasive carcinoma. J Biol Chem 286: 20778–20787.

    Article  CAS  Google Scholar 

  • Aziz MH, Hafeez BB, Sand JM, Pierce DB, Aziz SW, Dreckschmidt NE et al. (2010). Protein kinase C varepsilon mediates Stat3Ser727 phosphorylation, Stat3-regulated gene expression, and cell invasion in various human cancer cell lines through integration with MAPK cascade (RAF-1, MEK1/2, and ERK1/2). Oncogene 29: 3100–3109.

    Article  CAS  Google Scholar 

  • Bonner JA, Harari PM, Giralt J, Cohen RB, Jones CU, Sur RK et al. (2010). Radiotherapy plus cetuximab for locoregionally advanced head and neck cancer: 5-year survival data from a phase 3 randomised trial, and relation between cetuximab-induced rash and survival. Lancet Oncol 11: 21–28.

    Article  CAS  Google Scholar 

  • Calin GA, Croce CM . (2006). MicroRNA signatures in human cancers. Nat Rev Cancer 6: 857–866.

    Article  CAS  Google Scholar 

  • Cohen EE, Lingen MW, Zhu B, Zhu H, Straza MW, Pierce C et al. (2006). Protein kinase C zeta mediates epidermal growth factor-induced growth of head and neck tumor cells by regulating mitogen-activated protein kinase. Cancer Res 66: 6296–6303.

    Article  CAS  Google Scholar 

  • Cohen EE, Zhu H, Lingen MW, Martin LE, Kuo WL, Choi EA et al. (2009). A feed-forward loop involving protein kinase Calpha and microRNAs regulates tumor cell cycle. Cancer Res 69: 65–74.

    Article  CAS  Google Scholar 

  • Croce CM . (2009). Causes and consequences of microRNA dysregulation in cancer. Nat Rev Genet 10: 704–714.

    Article  CAS  Google Scholar 

  • Datta J, Kutay H, Nasser MW, Nuovo GJ, Wang B, Majumder S et al. (2008). Methylation mediated silencing of MicroRNA-1 gene and its role in hepatocellular carcinogenesis. Cancer Res 68: 5049–5058.

    Article  CAS  Google Scholar 

  • Dempsey EC, Newton AC, Mochly-Rosen D, Fields AP, Reyland ME, Insel PA et al. (2000). Protein kinase C isozymes and the regulation of diverse cell responses. Am J Physiol Lung Cell Mol Physiol 279: L429–L438.

    Article  CAS  Google Scholar 

  • Feng L, Xie Y, Zhang H, Wu Y . (2011). miR-107 targets cyclin-dependent kinase 6 expression, induces cell cycle G1 arrest and inhibits invasion in gastric cancer cells. Med Oncol (doi:10.1007/s12032-011-9823-1).

    Article  Google Scholar 

  • Filipowicz W, Bhattacharyya SN, Sonenberg N . (2008). Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight? Nat Rev Genet 9: 102–114.

    Article  CAS  Google Scholar 

  • Gutcher I, Webb PR, Anderson NG . (2003). The isoform-specific regulation of apoptosis by protein kinase C. Cell Mol Life Sci 60: 1061–1070.

    Article  CAS  Google Scholar 

  • Hwang HW, Mendell JT . (2006). MicroRNAs in cell proliferation, cell death, and tumorigenesis. Br J Cancer 94: 776–780.

    Article  CAS  Google Scholar 

  • Jaken S, Parker PJ . (2000). Protein kinase C binding partners. Bioessays 22: 245–254.

    Article  CAS  Google Scholar 

  • Kamangar F, Dores GM, Anderson WF . (2006). Patterns of cancer incidence, mortality, and prevalence across five continents: defining priorities to reduce cancer disparities in different geographic regions of the world. J Clin Oncol 24: 2137–2150.

    Article  Google Scholar 

  • Kozaki K, Imoto I, Mogi S, Omura K, Inazawa J . (2008). Exploration of tumor-suppressive microRNAs silenced by DNA hypermethylation in oral cancer. Cancer Res 68: 2094–2105.

    Article  CAS  Google Scholar 

  • Laramore GE, Scott CB, al-Sarraf M, Haselow RE, Ervin TJ, Wheeler R et al. (1992). Adjuvant chemotherapy for resectable squamous cell carcinomas of the head and neck: report on Intergroup Study 0034. Int J Radiat Oncol Biol Phys 23: 705–713.

    Article  CAS  Google Scholar 

  • Lee KH, Lotterman C, Karikari C, Omura N, Feldmann G, Habbe N et al. (2009). Epigenetic silencing of microRNA miR-107 regulates cyclin-dependent kinase 6 expression in pancreatic cancer. Pancreatology 9: 293–301.

    Article  CAS  Google Scholar 

  • Leemans CR, Braakhuis BJ, Brakenhoff RH . (2011). The molecular biology of head and neck cancer. Nat Rev Cancer 11: 9–22.

    Article  CAS  Google Scholar 

  • Li X, Zhang Y, Shi Y, Dong G, Liang J, Han Y et al. (2010). MicroRNA-107, an oncogene microRNA that regulates tumor invasion and metastasis by targeting DICER1 in gastric cancer: MiR-107 promotes gastric cancer invasion and metastasis. J Cell Mol Med 15: 1887–1895.

    Article  Google Scholar 

  • Liu X, Jiang L, Wang A, Yu J, Shi F, Zhou X . (2009). MicroRNA-138 suppresses invasion and promotes apoptosis in head and neck squamous cell carcinoma cell lines. Cancer Lett 286: 217–222.

    Article  CAS  Google Scholar 

  • Martello G, Rosato A, Ferrari F, Manfrin A, Cordenonsi M, Dupont S et al. (2010). A microRNA targeting dicer for metastasis control. Cell 141: 1195–1207.

    Article  CAS  Google Scholar 

  • Martinez-Gimeno C, Diaz-Meco MT, Dominguez I, Moscat J . (1995). Alterations in levels of different protein kinase C isotypes and their influence on behavior of squamous cell carcinoma of the oral cavity: epsilon PKC, a novel prognostic factor for relapse and survival. Head Neck 17: 516–525.

    Article  CAS  Google Scholar 

  • Nasser MW, Datta J, Nuovo G, Kutay H, Motiwala T, Majumder S et al. (2008). Down-regulation of micro-RNA-1 (miR-1) in lung cancer. Suppression of tumorigenic property of lung cancer cells and their sensitization to doxorubicin-induced apoptosis by miR-1. J Biol Chem 283: 33394–33405.

    Article  CAS  Google Scholar 

  • Pan Q, Bao LW, Teknos TN, Merajver SD . (2006). Targeted disruption of protein kinase C epsilon reduces cell invasion and motility through inactivation of RhoA and RhoC GTPases in head and neck squamous cell carcinoma. Cancer Res 66: 9379–9384.

    Article  CAS  Google Scholar 

  • Parkin DM . (2001). Global cancer statistics in the year 2000. Lancet Oncol 2: 533–543.

    Article  CAS  Google Scholar 

  • Wong TS, Liu XB, Wong BY, Ng RW, Yuen AP, Wei WI . (2008). Mature miR-184 as potential oncogenic microRNA of squamous cell carcinoma of tongue. Clin Cancer Res 14: 2588–2592.

    Article  CAS  Google Scholar 

  • Yamakuchi M, Lotterman CD, Bao C, Hruban RH, Karim B, Mendell JT et al. (2010). P53-induced microRNA-107 inhibits HIF-1 and tumor angiogenesis. Proc Natl Acad Sci USA 107: 6334–6339.

    Article  CAS  Google Scholar 

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Acknowledgements

This work was supported in part by the National Cancer Institute at the National Institutes of Health (R01CA135096); American Cancer Society (RSG0821901); the Michelle Theado Memorial Grant and the John Young Memorial Grant from the Joan Bisesi Fund for Head and Neck Oncology Research and the Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University Comprehensive Cancer Center.

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Datta, J., Smith, A., Lang, J. et al. microRNA-107 functions as a candidate tumor-suppressor gene in head and neck squamous cell carcinoma by downregulation of protein kinase Cɛ. Oncogene 31, 4045–4053 (2012). https://doi.org/10.1038/onc.2011.565

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