Prognostic Value of MiR-21: An Updated Meta-Analysis in Head and Neck Squamous Cell Carcinoma (HNSCC)
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, přehledy
PubMed
31766478
PubMed Central
PMC6947266
DOI
10.3390/jcm8122041
PII: jcm8122041
Knihovny.cz E-zdroje
- Klíčová slova
- bioinformatics analysis, head and neck cancer, miR-21, prognostic, survival,
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Head and neck squamous cell carcinoma (HNSCC) is a group of malignancies with serious impact on patient quality of life due to a reduced rate of response to chemotherapy or radiation therapy. MiR-21 has been identified as one of the most common proto-oncogenes. It is hypothesized that upregulated miR-21 could serve as a potential biomarker for human cancer diagnosis. Considering the target genes identified for miR-21 in HNSCC, this transcript is an important player in several cellular processes that control carcinogenesis. The abnormal expression of miR-21 in this group of pathologies has been assessed in several publications, but given the heterogeneity of the published results, a meta-analysis and proper bioinformatics analysis of expression databases are needed to correctly establish the prognostic potential of this molecule. The present meta-analysis comprises the published survival data on HNSCC patients, reported as HR and 95% CI, in association with the expression levels of miR-21. Our investigation revealed that miR-21 could be used successfully as a prognostic biomarker in HNSCC patients, confirming its oncogenic potential. Specifically, the upregulation of miR-21 in these patients predicts a worse outcome in terms of survival rate.
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Peltanova B., Raudenska M., Masarik M. Effect of tumor microenvironment on pathogenesis of the head and neck squamous cell carcinoma: A systematic review. Mol. Cancer. 2019;18:63. doi: 10.1186/s12943-019-0983-5. PubMed DOI PMC
Irimie A.I., Braicu C., Cojocneanu-Petric R., Berindan-Neagoe I., Campian R.S. Novel technologies for oral squamous carcinoma biomarkers in diagnostics and prognostics. Acta Odontol. Scand. 2015;73:161–168. doi: 10.3109/00016357.2014.986754. PubMed DOI
Kulasinghe A., Schmidt H., Perry C., Whitfield B., Kenny L., Nelson C., Warkiani M.E., Punyadeera C. A Collective Route to Head and Neck Cancer Metastasis. Sci. Rep. 2018;8:746. doi: 10.1038/s41598-017-19117-9. PubMed DOI PMC
Irimie A.I., Braicu C., Cojocneanu R., Magdo L., Onaciu A., Ciocan C., Mehterov N., Dudea D., Buduru S., Berindan-Neagoe I. Differential Effect of Smoking on Gene Expression in Head and Neck Cancer Patients. Int. J. Environ. Res. Public Health. 2018;15:1558. doi: 10.3390/ijerph15071558. PubMed DOI PMC
Irimie A.I., Sonea L., Jurj A., Mehterov N., Zimta A.A., Budisan L., Braicu C., Berindan-Neagoe I. Future trends and emerging issues for nanodelivery systems in oral and oropharyngeal cancer. Int. J. Nanomed. 2017;12:4593–4606. doi: 10.2147/IJN.S133219. PubMed DOI PMC
Kobayashi K., Hisamatsu K., Suzui N., Hara A., Tomita H., Miyazaki T. A Review of HPV-Related Head and Neck Cancer. J. Clin. Med. 2018;7:241. doi: 10.3390/jcm7090241. PubMed DOI PMC
Braicu C., Catana C., Calin G.A., Berindan-Neagoe I. NCRNA combined therapy as future treatment option for cancer. Curr. Pharm. Des. 2014;20:6565–6574. doi: 10.2174/1381612820666140826153529. PubMed DOI
Irimie A.I., Braicu C., Sonea L., Zimta A.A., Cojocneanu-Petric R., Tonchev K., Mehterov N., Diudea D., Buduru S., Berindan-Neagoe I. A Looking-Glass of Non-coding RNAs in oral cancer. Int. J. Mol. Sci. 2017;18:2620. doi: 10.3390/ijms18122620. PubMed DOI PMC
Ambros V. The functions of animal microRNAs. Nature. 2004;431:350–355. doi: 10.1038/nature02871. PubMed DOI
Bica-Pop C., Cojocneanu-Petric R., Magdo L., Raduly L., Gulei D., Berindan-Neagoe I. Overview upon miR-21 in lung cancer: Focus on NSCLC. Cell. Mol. Life Sci. CMLS. 2018;75:3539–3551. doi: 10.1007/s00018-018-2877-x. PubMed DOI PMC
Redis R.S., Berindan-Neagoe I., Pop V.I., Calin G.A. Non-coding RNAs as theranostics in human cancers. J. Cell. Biochem. 2012;113:1451–1459. doi: 10.1002/jcb.24038. PubMed DOI PMC
Sun S.-S., Zhou X., Huang Y.-Y., Kong L.-P., Mei M., Guo W.-Y., Zhao M.-H., Ren Y., Shen Q., Zhang L. Targeting STAT3/miR-21 axis inhibits epithelial-mesenchymal transition via regulating CDK5 in head and neck squamous cell carcinoma. Mol. Cancer. 2015;14:213. doi: 10.1186/s12943-015-0487-x. PubMed DOI PMC
Gao Y., Dai M., Liu H., He W., Lin S., Yuan T., Chen H., Dai S. Diagnostic value of circulating miR-21: An update meta-analysis in various cancers and validation in endometrial cancer. Oncotarget. 2016;7:68894–68908. doi: 10.18632/oncotarget.12028. PubMed DOI PMC
Liu T., Chen G., Sun D., Lei M., Li Y., Zhou C., Li X., Xue W., Wang H., Liu C., et al. Exosomes containing miR-21 transfer the characteristic of cisplatin resistance by targeting PTEN and PDCD4 in oral squamous cell carcinoma. Acta Biochim. Biophys. Sin. 2017;49:808–816. doi: 10.1093/abbs/gmx078. PubMed DOI
Wang W., Songlin P., Sun Y., Zhang B., Jinhui W. miR-21 inhibitor sensitizes human OSCC cells to cisplatin. Mol. Biol. Rep. 2012;39:5481–5485. doi: 10.1007/s11033-011-1350-9. PubMed DOI
Yan F., Wang C., Li T., Cai W., Sun J. Role of miR-21 in the growth and metastasis of human salivary adenoid cystic carcinoma. Mol. Med. Rep. 2018;17:4237–4244. doi: 10.3892/mmr.2018.8381. PubMed DOI PMC
Li J., Huang H., Sun L., Yang M., Pan C., Chen W., Wu D., Lin Z., Zeng C., Yao Y., et al. MiR-21 indicates poor prognosis in tongue squamous cell carcinomas as an apoptosis inhibitor. Clin. Cancer Res. 2009;15:3998–4008. doi: 10.1158/1078-0432.CCR-08-3053. PubMed DOI
Zhu H., Zhu X., Cheng G., Zhou M., Lou W. Downregulation of microRNA-21 enhances radiosensitivity in nasopharyngeal carcinoma. Exp. Ther. Med. 2015;9:2185–2189. doi: 10.3892/etm.2015.2403. PubMed DOI PMC
Yeh S.A. Radiotherapy for head and neck cancer. Semin. Plast. Surg. 2010;24:127–136. doi: 10.1055/s-0030-1255330. PubMed DOI PMC
Cen W.N., Pang J.S., Huang J.C., Hou J.Y., Bao W.G., He R.Q., Ma J., Peng Z.G., Hu X.H., Ma F.C. The expression and biological information analysis of miR-375-3p in head and neck squamous cell carcinoma based on 1825 samples from GEO, TCGA, and peer-reviewed publications. Pathol. Res. Pract. 2018;214:1835–1847. doi: 10.1016/j.prp.2018.09.010. PubMed DOI
Childs G., Fazzari M., Kung G., Kawachi N., Brandwein-Gensler M., McLemore M., Chen Q., Burk R.D., Smith R.V., Prystowsky M.B., et al. Low-level expression of microRNAs let-7d and miR-205 are prognostic markers of head and neck squamous cell carcinoma. Am. J. Pathol. 2009;174:736–745. doi: 10.2353/ajpath.2009.080731. PubMed DOI PMC
Avissar M., McClean M.D., Kelsey K.T., Marsit C.J. MicroRNA expression in head and neck cancer associates with alcohol consumption and survival. Carcinogenesis. 2009;30:2059–2063. doi: 10.1093/carcin/bgp277. PubMed DOI PMC
Hedback N., Jensen D.H., Specht L., Fiehn A.M., Therkildsen M.H., Friis-Hansen L., Dabelsteen E., von Buchwald C. MiR-21 expression in the tumor stroma of oral squamous cell carcinoma: An independent biomarker of disease free survival. PLoS ONE. 2014;9:e95193. doi: 10.1371/journal.pone.0095193. PubMed DOI PMC
Ko Y.H., Won H.S., Sun D.S., An H.J., Jeon E.K., Kim M.S., Lee H.H., Kang J.H., Jung C.K. Human papillomavirus-stratified analysis of the prognostic role of miR-21 in oral cavity and oropharyngeal squamous cell carcinoma. Pathol. Int. 2014;64:499–507. doi: 10.1111/pin.12201. PubMed DOI
Arantes L.M., Laus A.C., Melendez M.E., de Carvalho A.C., Sorroche B.P., De Marchi P.R., Evangelista A.F., Scapulatempo-Neto C., de Souza Viana L., Carvalho A.L. MiR-21 as prognostic biomarker in head and neck squamous cell carcinoma patients undergoing an organ preservation protocol. Oncotarget. 2017;8:9911–9921. doi: 10.18632/oncotarget.14253. PubMed DOI PMC
Yu E.H., Tu H.F., Wu C.H., Yang C.C., Chang K.W. MicroRNA-21 promotes perineural invasion and impacts survival in patients with oral carcinoma. J. Chin. Med Assoc. JCMA. 2017;80:383–388. doi: 10.1016/j.jcma.2017.01.003. PubMed DOI
Supic G., Zeljic K., Rankov A.D., Kozomara R., Nikolic A., Radojkovic D., Magic Z. miR-183 and miR-21 expression as biomarkers of progression and survival in tongue carcinoma patients. Clin. Oral Investig. 2018;22:401–409. doi: 10.1007/s00784-017-2126-y. PubMed DOI
Wang Y., Gao X., Wei F., Zhang X., Yu J., Zhao H., Sun Q., Yan F., Yan C., Li H., et al. Diagnostic and prognostic value of circulating miR-21 for cancer: A systematic review and meta-analysis. Gene. 2014;533:389–397. doi: 10.1016/j.gene.2013.09.038. PubMed DOI
Ishinaga H., He F., Hou B., Shah S., Murata M., Takeuchi K. A longitudinal study on circulating miR-21 as a therapeutic effect marker in head and neck squamous cell carcinoma. Carcinogenesis. 2019;40:1070–1076. doi: 10.1093/carcin/bgz075. PubMed DOI
He Q., Chen Z., Cabay R.J., Zhang L., Luan X., Chen D., Yu T., Wang A., Zhou X. microRNA-21 and microRNA-375 from oral cytology as biomarkers for oral tongue cancer detection. Oral Oncol. 2016;57:15–20. doi: 10.1016/j.oraloncology.2016.03.017. PubMed DOI PMC
Sun Z., Li S., Kaufmann A.M., Albers A.E. miR-21 increases the programmed cell death 4 gene-regulated cell proliferation in head and neck squamous carcinoma cell lines. Oncol. Rep. 2014;32:2283–2289. doi: 10.3892/or.2014.3456. PubMed DOI
Qiu Y.F., Wang M.X., Meng L.N., Zhang R., Wang W. MiR-21 regulates proliferation and apoptosis of oral cancer cells through TNF-alpha. Eur. Rev. Med. Pharmacol. Sci. 2018;22:7735–7741. doi: 10.26355/eurrev_201811_16395. PubMed DOI
Zheng Y., Xie J., Jiang F., Li Y., Chang G., Ma H. Inhibition of miR21 promotes cell apoptosis in oral squamous cell carcinoma by upregulating PTEN. Oncol. Rep. 2018;40:2798–2805. doi: 10.3892/or.2018.6663. PubMed DOI
Momen-Heravi F., Bala S. Extracellular vesicles in oral squamous carcinoma carry oncogenic miRNA profile and reprogram monocytes via NF-kappaB pathway. Oncotarget. 2018;9:34838–34854. doi: 10.18632/oncotarget.26208. PubMed DOI PMC
Ou H., Li Y., Kang M. Activation of miR-21 by STAT3 induces proliferation and suppresses apoptosis in nasopharyngeal carcinoma by targeting PTEN gene. PLoS ONE. 2014;9:e109929. doi: 10.1371/journal.pone.0109929. PubMed DOI PMC
Li Y., Yan L., Zhang W., Wang H., Chen W., Hu N., Ou H. miR-21 inhibitor suppresses proliferation and migration of nasopharyngeal carcinoma cells through down-regulation of BCL2 expression. Int. J. Clin. Exp. Pathol. 2014;7:3478–3487. PubMed PMC
Zheng G., Li N., Jia X., Peng C., Luo L., Deng Y., Yin J., Song Y., Liu H., Lu M., et al. MYCN-mediated miR-21 overexpression enhances chemo-resistance via targeting CADM1 in tongue cancer. J. Mol. Med. 2016;94:1129–1141. doi: 10.1007/s00109-016-1417-0. PubMed DOI
Kreimer A.R., Clifford G.M., Boyle P., Franceschi S. Human papillomavirus types in head and neck squamous cell carcinomas worldwide: A systematic review. Cancer Epidemiol. Biomark. Prev. 2005;14:467–475. doi: 10.1158/1055-9965.EPI-04-0551. PubMed DOI
Rampias T., Sasaki C., Weinberger P., Psyrri A. E6 and e7 gene silencing and transformed phenotype of human papillomavirus 16-positive oropharyngeal cancer cells. J. Natl. Cancer Inst. 2009;101:412–423. doi: 10.1093/jnci/djp017. PubMed DOI
Ragin C.C., Modugno F., Gollin S.M. The epidemiology and risk factors of head and neck cancer: A focus on human papillomavirus. J. Dent. Res. 2007;86:104–114. doi: 10.1177/154405910708600202. PubMed DOI
Kimple R.J., Smith M.A., Blitzer G.C., Torres A.D., Martin J.A., Yang R.Z., Peet C.R., Lorenz L.D., Nickel K.P., Klingelhutz A.J., et al. Enhanced radiation sensitivity in HPV-positive head and neck cancer. Cancer Res. 2013;73:4791–4800. doi: 10.1158/0008-5472.CAN-13-0587. PubMed DOI PMC