Cervical cancer is the second most common cancer among women world-wide, with about 470,000 newly diagnosed cases and almost 250,000 deaths every year. Furthermore, cervical cancer is the most common cause of death from gynecological malignancy in developing countries. Typically, type III radical hysterectomy (RH) is prescribed for patients diagnosed with stage IB-IIA cervical cancer who can tolerate an aggressive surgical approach, and want to avoid the long-term adverse effects of radiation therapy. For stage IIB patients, radiation therapy has been commonly prescribed. However, in some countries in Europe and Asia, type III radical hysterectomies are prescribed for patients with stage IB-IIB cervical cancer. Various clinico-pathological variables evaluated as possible prognostic factors for survival after RH, including depth of invasion, parametrial margin involvement, pelvic lymph node metastasis, number of lymph node metastases, histological type and pre-treatment squamous cell carcinoma (SQCC)-antigen level, are significant factors for clinical outcome. In addition to these clinico-pathologic variables, increasing attention has focused on various new approaches to molecular and genetic changes in cervical cancer. Molecular and genetic alterations are important in the pathogenesis of cervical cancer, especially in association with human papillomavirus (HPV) infections. One of considerable interest is c-MYC gene status. cMYC activation, triggered by insertion of HPV DNA sequences into near the c-MYC locus, is now regarded to be an important genetic event in cervical oncogenesis, c-MYC gene maps to chromosomal band 8q24, which is reportedly a common site for integration of HPV DNA. Gene amplification is an important mechanism for protein overexpression and oncogene activation in tumor cells. c-MYC amplification is well documented in cervical cancer. Amplification of the c-MYC gene is also addressed in breast cancer, bladder cancer, prostate cancer, and lung cancer. Although strong prognostic impact o f c-MYC gene amplification on histologic grade, disease stage and patients survival have been well documented in certain types of tumors, data on prognostic significance of both gain and amplification of c-MYC is lacking in cervical cancer. Therefore, in this study, we assessed c-MYC gene status in human cervical cancer samples using fluorescence in situ hybridization (FISH) to analyze the relation between c-MYC gene amplification and clinicopathologic factors. The prognostic value Prognostic Significance of Amplification of the c-MYC Gene in Surgically Treated Stage IB-IIB Cervical Cancer
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