Abstract

ObjectiveThis study is to investigate the role of miR-143 expression in cervical squamous cell carcinoma (SCC).MethodsThe expression level of miR-143 was examined by quantitative real-time PCR. Human papillomavirus (HPV) genotype was detected by HPV genotype detection kit. The expression level of bcl-2 was detected by immunohistochemistry.ResultsThe positive rate of HPV was 78% in the patients of cervical SCC. The most prevalent genotype was HPV16, with a positive rate of 42%. The expression level of miR-143 was significantly lower in the cervical SCC tissues than that in the normal cervical tissues (Z = −2.180, P = 0.029). Down-regulated miR-143 expression was associated with tumor size, lymph node metastasis and HPV16 infection in cervical cancer patients. No significant associations were found between the expression levels of miR-143 and age, clinical stage, differentiation or lymph vascular space invasion. And, in cervical SCC patients after treatment with Taxol chemotherapy, the expression level of miR-143 was higher and the positive expression of bcl-2 protein was lower. However, the differences in expression changes of miR-143 and bcl-2 were not statistically significant (miR-143, Z = −0.763, P = 0.446; bcl-2 protein, χ2 = 2.277, P = 0.131).ConclusionDown-regulated miR-143 is related with tumor size, lymph node metastasis and HPV16 infection in cervical SCC, but miR-143 does not participate in the Taxol sensitivity response.Virtual slidesThe virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1401279451112150.

Highlights

  • Cervical cancer is caused by the activation of oncogenes and the inactivation of tumor suppressor genes, which are induced by carcinogens through different mechanisms

  • This study aims to investigate the role of miR-143 expression in cervical squamous cell carcinoma (SCC) through detecting miR-143 expression, analyzing the relationship between miR-143 expression and clinical pathological features of cervical cancer, and assessing the sensitivity of miR-143 and bcl-2 expression to Taxol treatment

  • Quantitative results of miR-143 expression and its correlation with clinical pathological features of cervical SCC were shown in Figure 1 and Table 4

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Summary

Introduction

Cervical cancer is caused by the activation of oncogenes and the inactivation of tumor suppressor genes, which are induced by carcinogens through different mechanisms. Persistent infection of the human papillomavirus (HPV) is an important factor causing cervical cancer. Genes of E6 and E7 of HPV are able to inactivate the cellular tumor suppressor genes and induce the over expression of the anti-apoptotic genes. Besides HPV, factors from host cells are critical in the process of cervical malignant transformation. MicroRNAs (miRNAs) are a class of small, endogenous, single-stranded, non-coding RNA molecules, which can regulate cell proliferation, differentiation and apoptosis through targeting histology of cervical cancer [5]. MiR-143 plays an important role in cervical cancer

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