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X连锁凋亡抑制蛋白(XIAP)及XIAP相关因子-1在人肝细胞癌及癌旁肝组织中的表达及其与细胞凋亡的关系

X-linked inhibitor of apoptosis (XIAP) and XIAP-associated factor-1 expressions and their relationship to apoptosis in human hepatocellular carcinoma and non-cancerous liver tissues.

作者信息

Sakemi Ryosuke, Yano Hirohisa, Ogasawara Sachiko, Akiba Jun, Nakashima Osamu, Fukahori Suguru, Sata Michio, Kojiro Masamichi

机构信息

Department of Pathology, Kurume University School of Medicine, Fukuoka 830-0011, Japan.

出版信息

Oncol Rep. 2007 Jul;18(1):65-70.

Abstract

The X-linked inhibitor of apoptosis (XIAP) belongs to the inhibitor of apoptosis (IAP) family, and the action of XIAP is inhibited by XIAP-associated factor-1 (XAF1). In the present study, XIAP and XAF1 protein expressions and their relationship to apoptosis were investigated in hepatocellular carcinoma (HCC). We examined immunohistochemical expressions of XIAP and XAF1, and the number of apoptotic HCC cells in surgically resected tissues of 24 HCCs, consisting of 7 well-, 10 moderately and 7 poorly differentiated HCCs. As a result, XIAP and XAF1 expressions were identified in the cytoplasm of non-neoplastic and neoplastic hepatocytes. In the 24 HCCs, XIAP expression was not different according to the histological grade of HCC. In contrast, XAF1 expression was significantly lower in poorly differentiated than that in well- or moderately differentiated HCCs (P=0.001), or XIAP expression in poorly differentiated HCC (P<0.001). Apoptotic HCC cell number was significantly lower in poorly differentiated than that in well- or moderately differentiated HCCs (P<0.01). A significant relationship was observed between XAF1 expression and apoptotic cell number in HCC tissues. In conclusion, the present findings suggest that significantly low XAF1 expression, but not XIAP expression, in poorly differentiated HCC may relate to resistance to apoptosis.

摘要

X连锁凋亡抑制蛋白(XIAP)属于凋亡抑制蛋白(IAP)家族,XIAP的作用受到XIAP相关因子1(XAF1)的抑制。在本研究中,对肝细胞癌(HCC)中XIAP和XAF1的蛋白表达及其与凋亡的关系进行了研究。我们检测了24例HCC手术切除组织中XIAP和XAF1的免疫组化表达以及凋亡HCC细胞的数量,这些组织包括7例高分化、10例中分化和7例低分化HCC。结果显示,XIAP和XAF1在非肿瘤性和肿瘤性肝细胞的细胞质中均有表达。在这24例HCC中,XIAP的表达根据HCC的组织学分级并无差异。相反,低分化HCC中XAF1的表达明显低于高分化或中分化HCC(P = 0.001),或低分化HCC中XIAP的表达(P < 0.001)。低分化HCC中凋亡HCC细胞的数量明显低于高分化或中分化HCC(P < 0.01)。在HCC组织中观察到XAF1表达与凋亡细胞数量之间存在显著相关性。总之,目前的研究结果表明,低分化HCC中XAF1表达显著降低,但XIAP表达无此现象,这可能与凋亡抵抗有关。

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