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细胞外基质重塑、上皮间质转化和黏附分子在癌性神经侵袭中的作用:观点的转变。

The Role of ECM Remodeling, EMT, and Adhesion Molecules in Cancerous Neural Invasion: Changing Perspectives.

机构信息

Department of Genetics and Developmental BiologyRappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, 3525422, Israel.

Department of Otolaryngology-Head and Neck Surgery, University of California-San Francisco, Helen Diller Family Comprehensive Cancer Center, San Francisco, CA, 94158, USA.

出版信息

Adv Biol (Weinh). 2022 Sep;6(9):e2200039. doi: 10.1002/adbi.202200039. Epub 2022 Jul 7.

Abstract

Perineural invasion (PNI) refers to the cancerous invasion of nerves. It provides an alternative route for metastatic invasion and can exist independently in the absence of lymphatic or vascular invasion. It is a prominent characteristic of specific aggressive malignancies where it correlates with poor prognosis. The clinical significance of PNI is widely recognized despite a lack of understanding of the molecular mechanisms underlying its pathogenesis. The interaction between the nerve and the cancer cells is the most pivotal PNI step which is mediated by the activation or inhibition of multiple signaling pathways that include chemokines, interleukins, nerve growth factors, and matrix metalloproteinases, to name a few. The nerve-cancer cell interaction brings about specific changes in the perineural niche, which not only affects the regular nerve functions, but also enhances the migratory, invasive, and adherent properties of the tumor cells. This review aims to elucidate the vital role of adhesion molecules, extracellular matrix, and epithelial-mesenchymal proteins that promote PNI, which may serve as therapeutic targets in the future.

摘要

神经周围侵犯(PNI)是指癌症侵犯神经。它为转移侵袭提供了一种替代途径,并且可以在没有淋巴管或血管侵犯的情况下独立存在。它是某些侵袭性恶性肿瘤的显著特征,与预后不良相关。尽管人们对其发病机制的分子机制缺乏了解,但 PNI 的临床意义得到了广泛认可。神经和癌细胞之间的相互作用是 PNI 最重要的步骤,这是由多种信号通路的激活或抑制介导的,其中包括趋化因子、白细胞介素、神经生长因子和基质金属蛋白酶等。神经-癌细胞相互作用导致神经周围龛位发生特定变化,不仅影响正常的神经功能,还增强了肿瘤细胞的迁移、侵袭和黏附特性。本综述旨在阐明促进 PNI 的黏附分子、细胞外基质和上皮-间充质蛋白的重要作用,这些可能成为未来的治疗靶点。

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