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HMGB1 蛋白及其受体 RAGE 在人类恶性肿瘤中的表达。

The expression of HMGB1 protein and its receptor RAGE in human malignant tumors.

机构信息

Institute of Molecular Biology, Bulgarian Academy of Sciences, Sofia, Bulgaria.

出版信息

Mol Cell Biochem. 2010 Apr;337(1-2):251-8. doi: 10.1007/s11010-009-0305-0. Epub 2009 Oct 30.

Abstract

High Mobility Group Box 1 (HMGB1) is a nuclear non-histone protein discovered to be released in the extracellular medium as a response to various stimuli and implicated in cancerogenesis. High HMGB1 levels are reported in a variety of tumor types, but there are few data relating HMGB1 to the histological grade or to a particular cell type and cellular localization. We studied the expression of HMGB1 protein in malignant human tumors of different differentiation level and in tumor metastasis. In all tumor tissues, the protein level is elevated. In moderately differentiated carcinomas, the localization of the protein is perinuclear, while in the low differentiated; there is a tendency for non-specific nuclear localization. HMGB1 protein and its receptor RAGE are identified as a ligand-receptor pair that plays an important role in regulating the invasiveness of tumor cells. RAGE is not produced in all of the tested tumor specimens. We found high level of expression in hepatocellular, colorectal, and breast cribriform carcinomas, but not in malignant testicular specimens. Probably, the RAGE synthesis is related to distinctive tumor types. In metastatic cells, RAGE exhibits higher level of expression losing its specific granular cytosolic pattern characteristic for the primary tumors.

摘要

高迁移率族蛋白 B1(HMGB1)是一种核非组蛋白蛋白,被发现作为对各种刺激的反应而释放到细胞外基质中,并与癌症发生有关。在多种肿瘤类型中都报道了高 HMGB1 水平,但与组织学分级或特定细胞类型和细胞定位相关的数据很少。我们研究了 HMGB1 蛋白在不同分化水平的人类恶性肿瘤和肿瘤转移中的表达。在所有肿瘤组织中,蛋白质水平都升高了。在中度分化的癌中,蛋白质的定位是核周的,而在低分化的情况下,存在非特异性核定位的趋势。HMGB1 蛋白及其受体 RAGE 被鉴定为配体-受体对,在调节肿瘤细胞的侵袭性方面发挥重要作用。RAGE 并非在所有测试的肿瘤标本中都产生。我们发现肝细胞癌、结直肠癌和乳腺癌筛状癌中高表达,但恶性睾丸标本中不表达。可能,RAGE 的合成与独特的肿瘤类型有关。在转移性细胞中,RAGE 表达水平升高,失去了其对原发性肿瘤的特征性颗粒胞质模式。

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