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实体癌中的肿瘤芽生

Tumour budding in solid cancers.

作者信息

Lugli Alessandro, Zlobec Inti, Berger Martin D, Kirsch Richard, Nagtegaal Iris D

机构信息

Institute of Pathology, University of Bern, Bern, Switzerland.

Department of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

出版信息

Nat Rev Clin Oncol. 2021 Feb;18(2):101-115. doi: 10.1038/s41571-020-0422-y. Epub 2020 Sep 8.

Abstract

Tumour budding is an emerging prognostic biomarker in colorectal cancer (CRC) and other solid cancers. Tumour buds are usually defined as isolated single cancer cells or clusters of up to four cancer cells located at the invasive tumour front. The prognostic value of tumour budding is now supported by a large body of evidence, whereas the utility of this phenotype as a predictive biomarker remains under investigation. The application of tumour budding indices in clinical practice requires a standardized scoring system that can be tailored to specific tumour types and clinical scenarios. In the context of CRC, tumour budding can be assessed according to the method agreed at the International Tumour Budding Consensus Conference (ITBCC) in 2016. Using the ITBCC scoring system, tumour budding is an independent predictor of lymph node metastasis in patients with pT1 CRC and of unfavourable survival in patients with stage II colon cancer. Regardless of the clinical scenario or tumour type, the assertion that 'the more tumour buds, the worse the clinical outcome' applies. In this Review, we provide an overview of tumour budding in solid cancers, highlighting the molecular and biological aspects of this phenomenon, including its associations with epithelial-mesenchymal transition and features of the tumour microenvironment. We also describe the available evidence demonstrating the value of tumour budding as a biomarker across various solid cancers.

摘要

肿瘤芽生是结直肠癌(CRC)和其他实体癌中一种新出现的预后生物标志物。肿瘤芽通常被定义为位于侵袭性肿瘤前沿的孤立单个癌细胞或由多达四个癌细胞组成的细胞簇。目前,大量证据支持肿瘤芽生的预后价值,而这种表型作为预测性生物标志物的效用仍在研究中。在临床实践中应用肿瘤芽生指数需要一个标准化的评分系统,该系统可根据特定肿瘤类型和临床情况进行调整。在CRC中,可根据2016年国际肿瘤芽生共识会议(ITBCC)商定的方法评估肿瘤芽生。使用ITBCC评分系统,肿瘤芽生是pT1 CRC患者淋巴结转移以及II期结肠癌患者不良生存的独立预测因素。无论临床情况或肿瘤类型如何,“肿瘤芽越多,临床结果越差”这一论断都适用。在本综述中,我们概述了实体癌中的肿瘤芽生,强调了这一现象的分子和生物学方面,包括其与上皮-间质转化的关联以及肿瘤微环境的特征。我们还描述了现有证据,证明肿瘤芽生作为各种实体癌生物标志物的价值。

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