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在高级别浆液性卵巢癌中,YKL-40 蛋白的组织免疫表达增加。

Increased tissue immunoexpression of YKL-40 protein in high grade serous ovarian cancers.

机构信息

Department of Nephropathology, Medical University of Lodz, ul. Pomorska 251, 92-213 Lodz, Poland.

出版信息

Pathol Res Pract. 2011 Sep 15;207(9):573-6. doi: 10.1016/j.prp.2011.06.008. Epub 2011 Aug 5.

Abstract

YKL-40 is a glycoprotein secreted by numerous human cells, such as cartilage, synovial, and endothelial cells. The biological role of YKL-40 has not yet been fully unveiled, however, its participation is perceived in angiogenesis, growth, proliferation, differentiation, and remodeling processes. The primary goal of our study was to evaluate possible differences in tissue immunoexpression of YKL-40, assumed between high grade and low-grade ovarian cancers and between the above-mentioned cancer types and benign lesions. Another purpose was to find out whether immunoexpression of the studied protein could correlate with the tumor proliferation process, evaluated by Ki-67 immunoexpression. The analysis comprised 45 women, diagnosed and treated for epithelial ovarian tumors at the Medical University of Lodz between 1997 and 2002. YKL-40 protein immunoexpression was semiquantitatively assessed, whereas immunoexpression of Ki-67 was evaluated using a computer image analysis system. Significantly higher immunoexpression values of both examined proteins were observed in high-grade serous ovarian cancers vs. low-grade and benign tumors. Moreover, a significant positive correlation was identified between the immunoexpressions of YKL-40 and Ki-67 proteins in the studied groups of tumors. In conclusion, the obtained data suggest an overt prominence of TKL-40 tissue immunoexpression of YKL-40 in high-grade serous ovarian tumors, which could then be approached as a helpful, additional marker to identify more aggressive ovarian cancers.

摘要

YKL-40 是一种糖蛋白,由许多人类细胞分泌,如软骨、滑膜和内皮细胞。YKL-40 的生物学作用尚未完全揭示,但它参与了血管生成、生长、增殖、分化和重塑过程。我们的主要研究目的是评估 YKL-40 在组织免疫表达方面在高级别和低级别卵巢癌之间以及上述癌症类型与良性病变之间可能存在的差异。另一个目的是确定研究蛋白的免疫表达是否与肿瘤增殖过程相关,该过程通过 Ki-67 免疫表达来评估。该分析包括 45 名女性,她们于 1997 年至 2002 年在罗兹医科大学被诊断和治疗上皮性卵巢肿瘤。使用计算机图像分析系统对 YKL-40 蛋白免疫表达进行半定量评估,对 Ki-67 免疫表达进行评估。在高级别浆液性卵巢癌与低级别和良性肿瘤相比,两种被检查蛋白的免疫表达值显著更高。此外,在研究的肿瘤组中,YKL-40 和 Ki-67 蛋白的免疫表达之间存在显著的正相关。总之,获得的数据表明 YKL-40 在高级别浆液性卵巢癌中的组织免疫表达明显突出,因此可以作为识别更具侵袭性卵巢癌的有用附加标志物。

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