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液体活检在黑色素瘤和默克尔细胞癌中的临床相关性

Clinical Relevance of Liquid Biopsy in Melanoma and Merkel Cell Carcinoma.

作者信息

Boyer Magali, Cayrefourcq Laure, Dereure Olivier, Meunier Laurent, Becquart Ondine, Alix-Panabières Catherine

机构信息

Laboratory of Rare Human Circulating Cells, University Medical Centre of Montpellier, 34093 Montpellier, France.

Department of Dermatology and INSERM 1058 Pathogenesis and Control of Chronic Infections, University of Montpellier, 34090 Montpellier, France.

出版信息

Cancers (Basel). 2020 Apr 13;12(4):960. doi: 10.3390/cancers12040960.

Abstract

Melanoma and Merkel cell carcinoma are two aggressive skin malignancies with high disease-related mortality and increasing incidence rates. Currently, invasive tumor tissue biopsy is the gold standard for their diagnosis, and no reliable easily accessible biomarker is available to monitor patients with melanoma or Merkel cell carcinoma during the disease course. In these last years, liquid biopsy has emerged as a candidate approach to overcome this limit and to identify biomarkers for early cancer diagnosis, prognosis, therapeutic response prediction, and patient follow-up. Liquid biopsy is a blood-based non-invasive procedure that allows the sequential analysis of circulating tumor cells, circulating cell-free and tumor DNA, and extracellular vesicles. These innovative biosources show similar features as the primary tumor from where they originated and represent an alternative to invasive solid tumor biopsy. In this review, the biology and technical challenges linked to the detection and analysis of the different circulating candidate biomarkers for melanoma and Merkel cell carcinoma are discussed as well as their clinical relevance.

摘要

黑色素瘤和默克尔细胞癌是两种侵袭性皮肤恶性肿瘤,疾病相关死亡率高且发病率不断上升。目前,侵入性肿瘤组织活检是其诊断的金标准,在黑色素瘤或默克尔细胞癌患者的病程中,尚无可靠且易于获取的生物标志物用于监测。近年来,液体活检已成为一种有望克服这一局限并识别早期癌症诊断、预后、治疗反应预测及患者随访生物标志物的方法。液体活检是一种基于血液的非侵入性检测手段,可对循环肿瘤细胞、循环游离肿瘤DNA及细胞外囊泡进行连续分析。这些创新的生物样本源与其起源的原发性肿瘤具有相似特征,是侵入性实体肿瘤活检的替代方法。在本综述中,我们将讨论与黑色素瘤和默克尔细胞癌不同循环候选生物标志物的检测和分析相关的生物学及技术挑战,以及它们的临床相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4a2/7226137/dbb97a83333d/cancers-12-00960-g001.jpg

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