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紧密连接蛋白7在嫌色性肾细胞癌和肾嗜酸细胞瘤中高表达。

Claudin-7 is highly expressed in chromophobe renal cell carcinoma and renal oncocytoma.

作者信息

Choi Yoo Duk, Kim Ki Seung, Ryu Sunhyo, Park Youngkyu, Cho Nam Hoon, Rha Seo Hee, Jang Ja June, Ro Jae Y, Juhng Sang Woo, Choi Chan

机构信息

Department of Pathology, Chonnam National University Medical School, 5 Hak-dong, Dong-gu, Gwangju, Korea.

出版信息

J Korean Med Sci. 2007 Apr;22(2):305-10. doi: 10.3346/jkms.2007.22.2.305.

Abstract

Claudin-7 has recently been suggested to be a distal nephron marker. We tested the possibility that expression of claudin-7 could be used as a marker of renal tumors originating from the distal nephron. We examined the immunohistochemical expression of claudin-7 and parvalbumin in 239 renal tumors, including 179 clear cell renal cell carcinoma (RCC)s, 29 papillary RCCs, 20 chromophobe RCCs, and 11 renal oncocytomas. In addition, the methylation specific-PCR (MSP) of claudin-7 was performed. Claudin-7 and parvalbumin immunostains were positive in 3.4%, 7.8% of clear cell RCCs, 34.5%, 31.0% of papillary RCCs, 95.0%, 80.0% of chromophobe RCCs, and 72.7%, 81.8% of renal oncocytomas, respectively. The sensitivity and specificity of claudin-7 in diagnosing chromophobe RCC among subtypes of RCC were 95.0% and 92.3%. Those of parvalbumin were 80.0% and 88.9%. The expression pattern of claudin-7 was mostly diffuse in chromophobe RCC and was either focal or diffuse in oncocytoma. All of the cases examined in the MSP revealed the presence of unmethylated promoter of claudin-7 without regard to claudin-7 immunoreactivity. Hypermethylation of the promoter might not be the underlying mechanism for loss of its expression in RCC. Claudin-7 can be used as a useful diagnostic marker in diagnosing chromophobe RCC and oncocytoma.

摘要

Claudin-7最近被认为是远曲小管标志物。我们测试了Claudin-7表达能否用作源自远曲小管的肾肿瘤标志物的可能性。我们检测了239例肾肿瘤中Claudin-7和小清蛋白的免疫组化表达,其中包括179例透明细胞肾细胞癌(RCC)、29例乳头状RCC、20例嫌色性RCC和11例肾嗜酸细胞瘤。此外,还进行了Claudin-7的甲基化特异性PCR(MSP)检测。Claudin-7和小清蛋白免疫染色在透明细胞RCC中的阳性率分别为3.4%、7.8%,在乳头状RCC中分别为34.5%、31.0%,在嫌色性RCC中分别为95.0%、80.0%,在肾嗜酸细胞瘤中分别为72.7%、81.8%。Claudin-7在RCC各亚型中诊断嫌色性RCC的敏感性和特异性分别为95.0%和92.3%。小清蛋白的敏感性和特异性分别为80.0%和88.9%。Claudin-7的表达模式在嫌色性RCC中大多为弥漫性,在嗜酸细胞瘤中可为局灶性或弥漫性。MSP检测的所有病例均显示Claudin-7启动子未甲基化,与Claudin-7免疫反应性无关。启动子的高甲基化可能不是其在RCC中表达缺失的潜在机制。Claudin-7可作为诊断嫌色性RCC和嗜酸细胞瘤的有用诊断标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac6e/2693599/e95b0fbf884d/jkms-22-305-g001.jpg

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