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CD44及其配体透明质酸作为恶性胸膜间皮瘤潜在生物标志物:证据与展望

CD44 and its ligand hyaluronan as potential biomarkers in malignant pleural mesothelioma: evidence and perspectives.

作者信息

Cortes-Dericks Lourdes, Schmid Ralph Alexander

机构信息

Department of Clinical Research, Division of General Thoracic Surgery, University Hospital Berne, Berne, Switzerland.

出版信息

Respir Res. 2017 Apr 12;18(1):58. doi: 10.1186/s12931-017-0546-5.

Abstract

Malignant pleural mesothelioma (MPM) is a rare and highly drug resistant tumor arising from the mesothelial surfaces of the lung pleura. The standard method to confirm MPM is the tedious, time-consuming cytological examination of cancer biopsy. Biomarkers that are detectable in pleural effusion or patient serum are reasonable options to provide a faster and noninvasive diagnostic approach. As yet, the current biomarkers for MPM lack specificity and sensitivity to discriminate this neoplasm from other lung tumors. CD44, a multifunctional surface receptor has been implicated in tumor progression in different cancers including MPM. The interaction of CD44 with its ligand, hyaluronan (HA) has demonstrated an important role in modulating cell proliferation and invasiveness in MPM. In particular, the high expression levels of these molecules have shown diagnostic relevance in MPM. This review will summarize the biology and diagnostic implication of CD44 and HA as well as the interaction of both molecules in MPM that will demonstrate their potential as biomarkers. Augmentation of the current markers in MPM may lead to an earlier diagnosis and management of this disease.

摘要

恶性胸膜间皮瘤(MPM)是一种罕见且具有高度耐药性的肿瘤,起源于肺胸膜的间皮表面。确诊MPM的标准方法是对癌组织活检进行繁琐、耗时的细胞学检查。在胸腔积液或患者血清中可检测到的生物标志物是提供更快且非侵入性诊断方法的合理选择。然而,目前用于MPM的生物标志物缺乏特异性和敏感性,难以将这种肿瘤与其他肺部肿瘤区分开来。CD44是一种多功能表面受体,在包括MPM在内的不同癌症的肿瘤进展中发挥作用。CD44与其配体透明质酸(HA)的相互作用在调节MPM细胞增殖和侵袭性方面显示出重要作用。特别是,这些分子的高表达水平在MPM中具有诊断意义。本综述将总结CD44和HA的生物学特性及诊断意义,以及这两种分子在MPM中的相互作用,这将证明它们作为生物标志物的潜力。增强MPM中当前标志物的检测可能会实现对该疾病的早期诊断和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec91/5389171/41194adf8ea6/12931_2017_546_Fig1_HTML.jpg

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