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Cathepsin K expression in the spectrum of perivascular epithelioid cell (PEC) lesions of the kidney

机译:肾脏的血管周上皮样细胞(PEC)病变谱中的组织蛋白酶K表达

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The perivascular epithelioid cell (PEC) is a unique cell type coexpressing contractile proteins (mainly α-smooth muscle actin), melanocytic markers, including microphthalmia-associated transcription factor (MITF), and estrogen and progesterone receptors. It is constantly present in a group of tumors called PEComas. Renal PEComas include the common angiomyolipoma as well as less common lesions such as microscopic angiomyolipoma, intraglomerular lesions, angiomyolipoma with epithelial cysts, epithelioid angiomyolipoma, oncocytoma-like angiomyolipoma and lymphangioleiomyomatosis of the renal sinus. It has been demonstrated that most of these lesions are determined by mutations affecting genes of the tuberous sclerosis complex, tuberous sclerosis 1 (TSC1) and tuberous sclerosis 2 (TSC2), with eventual deregulation of the RHEB/MTOR/RPS6KB2 pathway, and it has been observed that some PEComas regressed during sirolimus therapy, an MTOR inhibitor. Recently, overexpression of MITF has been related to the expression of the papain-like cysteine protease cathepsin K in osteoclasts where it has inhibited MTOR. The aim of this study is to evaluate cathepsin K immunohistochemically in the entire spectrum of PEComa lesions in the kidney. The study population consisted of 84 renal PEComa lesions, including 5 composed predominantly of fat (lipoma-like angiomyolipoma), 15 almost exclusively composed of spindle-shaped smooth muscle cells (leiomyoma-like angiomyolipoma) and 31 common angiomyolipomas composed of a mixture of fat, spindle and epithelioid smooth muscle cells, and abnormal thick-walled blood vessels, 15 microscopic angiomyolipomas, 5 intraglomerular lesions, 2 oncocytoma-like angiomyolipomas, 8 epithelioid angiomyolipomas, 2 angiomyolipomas with epithelial cysts and 1 example of lymphangioleiomyomatosis of the renal sinus. In all of the renal PEComas, cathepsin K was found to be constantly and strongly expressed and seems to be a more powerful marker than other commonly used markers for their identification, especially to confirm the diagnosis on needle biopsies.
机译:血管周上皮样细胞(PEC)是一种独特的细胞类型,可共表达收缩蛋白(主要是α平滑肌肌动蛋白),黑素细胞标志物,包括小眼症相关转录因子(MITF)以及雌激素和孕激素受体。它持续存在于称为PEComas的一组肿瘤中。肾脏PEComas包括常见的血管平滑肌脂肪瘤以及较不常见的病变,例如镜下血管平滑肌脂肪瘤,肾小球内病变,具有上皮囊肿的血管平滑肌脂肪瘤,上皮样血管平滑肌脂肪瘤,类癌细胞瘤血管平滑肌脂肪瘤和肾窦的淋巴管血管平滑肌瘤病。已经证明,大多数这些病变是由影响结节性硬化复合物,结节性硬化1(TSC1)和结节性硬化2(TSC2)基因的突变决定的,并且最终使RHEB / MTOR / RPS6KB2通路失控。有人观察到,在Miro抑制剂西罗莫司治疗期间,一些PEComas退化。最近,MITF的过表达与破骨细胞中木瓜蛋白酶样半胱氨酸蛋白酶组织蛋白酶K的表达有关,在破骨细胞中它抑制了MTOR。这项研究的目的是通过免疫组织化学方法在肾脏PEComa病变的整个范围内评估组织蛋白酶K。研究人群包括84个肾脏PEComa病变,其中5个主要由脂肪组成(脂瘤样血管肌脂瘤),15个几乎仅由纺锤形平滑肌细胞组成(平滑肌瘤样血管肌脂瘤)和31个由脂肪混合物组成的常见血管肌脂瘤,梭形和上皮样平滑肌细胞,异常的厚壁血管,15个显微血管平滑肌脂肪瘤,5个肾小球内病变,2个嗜细胞瘤样血管平滑肌脂肪瘤,8个上皮样血管平滑肌脂肪瘤,2个具有上皮囊肿的血管平滑肌脂肪瘤和1个肾窦淋巴管平滑肌瘤病。在所有的肾脏PEComas中,发现组织蛋白酶K持续且强烈表达,并且似乎是比其他常用标记更强大的标记,可用于识别它们,尤其是用于确认穿刺活检的诊断。

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