首页> 外文期刊>International journal of gynecological cancer: official journal of the International Gynecological Cancer Society >Overexpression of cyclin D1 and c-Myc gene products in human primary epithelial ovarian cancer.
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Overexpression of cyclin D1 and c-Myc gene products in human primary epithelial ovarian cancer.

机译:人原发性上皮性卵巢癌中细胞周期蛋白D1和c-Myc基因产物的过表达。

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摘要

Cyclin D1 and c-Myc are key participants in the cell-cycle pathway, in which aberrancies have been associated with malignant transformation. To date, data on the relationship of expression of these proteins and histologic subtype of epithelial ovarian cancer are still scarce and discordant. Immunohistochemical analysis was performed on 12 normal ovaries and 47 cases of serous, mucinous, endometrioid, and clear cell ovarian carcinomas. No abnormal expression of cyclin D1 or c-Myc was demonstrated in any of the 12 normal ovarian specimens. However, compared to normal ovarian tissues, overexpression of cyclin D1 and c-Myc was observed in 42.6% (20/47) and 65.9% (31/47) of tumors examined, respectively. There was no significant difference of overexpression of cyclin D1 or c-Myc gene products between these four histologic subtypes of ovarian adenocarcinomas. This study shows that cyclin D1 and c-Myc are frequently overexpressed in epithelial ovarian carcinomas, but they are not correlated with a particular histologic subtype. Although our preliminary results need to be validated in a larger number of tumors, the abnormal expression of cyclin D1 and c-Myc in epithelial ovarian cancer reaffirms the notion that they are crucial components in the pathway of tumorigenesis and deserve further study.
机译:细胞周期蛋白D1和c-Myc是细胞周期途径的关键参与者,其中畸变与恶性转化有关。迄今为止,关于这些蛋白质表达与上皮性卵巢癌的组织学亚型之间关系的数据仍然很少且不一致。对12例正常卵巢和47例浆液性,粘液性,子宫内膜样和透明细胞性卵巢癌病例进行了免疫组织化学分析。在12例正常卵巢标本中均未显示出细胞周期蛋白D1或c-Myc的异常表达。然而,与正常卵巢组织相比,在所检查的肿瘤中分别观察到细胞周期蛋白D1和c-Myc的过表达为42.6%(20/47)和65.9%(31/47)。在这四种卵巢腺癌的组织学亚型之间,cyclin D1或c-Myc基因产物的过表达没有显着差异。这项研究表明,cyclin D1和c-Myc在上皮性卵巢癌中经常过表达,但与特定的组织学亚型无关。尽管我们的初步结果需要在更多的肿瘤中得到验证,但cyclin D1和c-Myc在卵巢上皮癌中的异常表达再次证实了它们是肿瘤发生途径中至关重要的组成部分的观点,值得进一步研究。

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