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高迁移率族蛋白盒1与晚期糖基化终末产物受体与血液系统恶性肿瘤临床病理特征的相关性:一项系统综述

Association of high mobility group BOX-1 and receptor for advanced glycation endproducts with clinicopathological features of haematological malignancies: a systematic review.

作者信息

Nguyen Austin H, Bhavsar Sheila B, Riley Erinn M, Caponetti Gabriel C, Agrawal Devendra K

机构信息

Department of Clinical and Translational Science, Creighton University School of Medicine, Omaha NE, United States.

Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.

出版信息

Contemp Oncol (Pozn). 2016;20(6):425-429. doi: 10.5114/wo.2016.65600. Epub 2017 Jan 12.

Abstract

High-mobility group box 1 (HMGB1) is a versatile protein with nuclear and extracellular functions. In the extracellular milieu, HMGB1 binds to several receptors, notably the receptor for advanced glycation end-products (RAGE). The expressions of HMGB1 and RAGE have been described in a variety of cancers. However, the clinical values of HMGB1 and RAGE in haematological malignancies have yet to be evaluated. A systematic search through PubMed and the Web of Science for articles discussing the role of HMGB1 and RAGE in haematological malignancies produced 15 articles. Overexpression of HMGB1 was reported to be associated with malignancy and, in certain studies, poor prognosis and tumour aggressiveness. Only one included study investigated the clinical value of RAGE, in which no significant difference was found between expression of RAGE in CLL neoplastic cells and nonmalignant controls. The discussed associations of HMGB1 and RAGE with clinicopathological characteristics of patients with haematological malignancies warrants further investigation into the prognostic and diagnostic value of both of these molecules.

摘要

高迁移率族蛋白B1(HMGB1)是一种具有核内和细胞外功能的多功能蛋白质。在细胞外环境中,HMGB1可与多种受体结合,尤其是晚期糖基化终产物受体(RAGE)。HMGB1和RAGE在多种癌症中均有表达。然而,HMGB1和RAGE在血液系统恶性肿瘤中的临床价值尚未得到评估。通过PubMed和Web of Science系统检索讨论HMGB1和RAGE在血液系统恶性肿瘤中作用的文章,共检索到15篇文章。据报道,HMGB1的过表达与恶性肿瘤相关,在某些研究中还与预后不良和肿瘤侵袭性有关。纳入的研究中仅有一项调查了RAGE的临床价值,结果发现慢性淋巴细胞白血病(CLL)肿瘤细胞中RAGE的表达与非恶性对照之间无显著差异。HMGB1和RAGE与血液系统恶性肿瘤患者临床病理特征之间的上述关联,值得进一步研究这两种分子的预后和诊断价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4114/5320453/dd3695a8db3e/WO-20-29314-g001.jpg

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