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首页> 外文期刊>German Medical Science >Detection of HER-2eu, c-myc amplification and p53 inactivation by FISH in Egyptian patients with breast cancer
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Detection of HER-2eu, c-myc amplification and p53 inactivation by FISH in Egyptian patients with breast cancer

机译:通过FISH检测埃及乳腺癌患者的HER-2 / neu,c-myc扩增和p53失活

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Breast cancer is a leading cause of cancer-related deaths in women worldwide. The clinical course of this disease is highly variable and clinicians continuously search for prognostic parameters that can accurately predict prognosis, and indicate a suitable adjuvant therapy for each patient. Amplification of the two oncogenes HER-2eu and c-myc and inactivation of the tumor suppressor gene p53 are frequently encountered in breast carcinomas. The purpose of this study was to use the fluorescence in situ hybridization (FISH) for the assessment of HER-2eu and c-myc amplification and p53 inactivation and to relate these molecular markers with the commonly used clinical and pathological factors. The study was conducted on 34 tissue samples obtained from 33 females and 1 male with breast carcinomas and 17 samples obtained from 16 females and 1 male with benign breast lesions. Results revealed that the level of HER-2eu, c-myc and p53 in the malignant group was significantly increased as compared to the benign group. On relating the level of the molecular markers to clinicopathological factors, p53 was significantly associated with increased patient’s age. The sensitivity of the investigated markers significantly increased with larger tumor size. Concerning tumor grade, HER-2eu and p53 showed a significant increase in low-grade tumors whereas c-myc showed a highly significant increase in high-grade tumors. With regard to disease staging, HER-2eu and c-myc were the only markers that showed significant increase at late stages of disease. p53 and HER-2eu were significantly associated with positive lymph nodal status. A significant correlation was obtained between the levels of the three biomarkers to each other. Conclusively, the combination of HER-2eu, c-myc and p53 can stratify patients into different risk groups.
机译:乳腺癌是全世界女性与癌症相关的死亡的主要原因。该疾病的临床过程变化很大,临床医生不断寻找可以准确预测预后的预后参数,并为每位患者指明合适的辅助治疗方法。在乳腺癌中经常遇到两种癌基因HER-2 / neu和c-myc的扩增以及肿瘤抑制基因p53的失活。这项研究的目的是使用荧光原位杂交(FISH)评估HER-2 / neu和c-myc扩增以及p53失活,并将这些分子标记物与常用的临床和病理因素相关联。该研究对从33例女性和1例男性乳腺癌组织中获得的34个组织样本以及从16例女性和1例具有良性乳腺病变男性中获得的组织样本进行了研究。结果显示,与良性组相比,恶性组的HER-2 / neu,c-myc和p53水平显着升高。在将分子标记物的水平与临床病理因素联系起来时,p53与患者年龄的增加显着相关。随着肿瘤尺寸的增大,所研究标记物的敏感性显着提高。关于肿瘤级别,HER-2 / neu和p53在低级别肿瘤中显着增加,而c-myc在高级肿瘤中显着增加。关于疾病分期,HER-2 / neu和c-myc是仅有的在疾病晚期显示出明显增加的标志物。 p53和HER-2 / neu与阳性淋巴结状态显着相关。三种生物标志物的水平之间存在显着相关性。结论是,HER-2 / neu,c-myc和p53的组合可以将患者分为不同的风险组。

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