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针对套细胞淋巴瘤治疗中肿瘤细胞微环境的靶向治疗原理。

Rationale for targeting tumor cells in their microenvironment for mantle cell lymphoma treatment.

作者信息

Papin Antonin, Le Gouill Steven, Chiron David

机构信息

a CRCINA, INSERM, CNRS , Université de Nantes, Université d'Angers , Nantes , France.

b GDR3697 Micronit , CNRS , Nantes , France.

出版信息

Leuk Lymphoma. 2018 May;59(5):1064-1072. doi: 10.1080/10428194.2017.1357177. Epub 2017 Jul 31.

Abstract

Mantle cell lymphoma (MCL) is an aggressive non-Hodgkin lymphoma associated with poor prognosis, and despite recent improvements in the therapeutic strategies for treating MCL, its management remains challenging. While improvements in next generation sequencing technology have greatly increased our understanding of the intrinsic abnormalities of MCL, the role of extrinsic signaling remains largely unknown. Recent studies have highlighted the central role of the MCL microenvironment in tumor cell survival, drug resistance and proliferation. Characterization of the diverse MCL tumoral niches and comprehension of the crosstalk between tumor cells and surrounding cells within the MCL microenvironment are needed to increase treatment efficacy. Here, we reviewed the recent findings regarding the MCL microenvironment that could be rapidly translated into new therapeutic strategies to overcome drug resistance during MCL treatment.

摘要

套细胞淋巴瘤(MCL)是一种侵袭性非霍奇金淋巴瘤,预后较差,尽管近年来MCL的治疗策略有所改进,但其管理仍然具有挑战性。虽然新一代测序技术的进步极大地增进了我们对MCL内在异常的理解,但外在信号传导的作用在很大程度上仍不清楚。最近的研究强调了MCL微环境在肿瘤细胞存活、耐药性和增殖中的核心作用。需要对不同的MCL肿瘤龛进行表征,并理解MCL微环境中肿瘤细胞与周围细胞之间的相互作用,以提高治疗效果。在此,我们综述了关于MCL微环境的最新研究结果,这些结果可迅速转化为新的治疗策略,以克服MCL治疗期间的耐药性。

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