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癌症相关成纤维细胞:致瘤性及癌症治疗靶点

Cancer-Associated Fibroblasts: Tumorigenicity and Targeting for Cancer Therapy.

作者信息

Glabman Raisa A, Choyke Peter L, Sato Noriko

机构信息

Molecular Imaging Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Department of Comparative Medicine and Integrative Biology, College of Veterinary Medicine, Michigan State University, East Lansing, MI 48824, USA.

出版信息

Cancers (Basel). 2022 Aug 12;14(16):3906. doi: 10.3390/cancers14163906.

Abstract

Cancer-associated fibroblasts (CAFs) are a heterogenous group of activated fibroblasts and a major component of the tumor stroma. CAFs may be derived from fibroblasts, epithelial cells, endothelial cells, cancer stem cells, adipocytes, pericytes, or stellate cells. These complex origins may underlie their functional diversity, which includes pro-tumorigenic roles in extracellular matrix remodeling, the suppression of anti-tumor immunity, and resistance to cancer therapy. Several methods for targeting CAFs to inhibit tumor progression and enhance anti-tumor immunity have recently been reported. While preclinical studies have shown promise, to date they have been unsuccessful in human clinical trials against melanoma, breast cancer, pancreas cancer, and colorectal cancers. This review summarizes recent and major advances in CAF-targeting therapies, including DNA-based vaccines, anti-CAF CAR-T cells, and modifying and reprogramming CAF functions. The challenges in developing effective anti-CAF treatment are highlighted, which include CAF heterogeneity and plasticity, the lack of specific target markers for CAFs, the limitations in animal models recapitulating the human cancer microenvironment, and the undesirable off-target and systemic side effects. Overcoming these challenges and expanding our understanding of the basic biology of CAFs is necessary for making progress towards safe and effective therapeutic strategies against cancers in human patients.

摘要

癌症相关成纤维细胞(CAFs)是一群异质性的活化成纤维细胞,也是肿瘤基质的主要组成部分。CAFs可能来源于成纤维细胞、上皮细胞、内皮细胞、癌症干细胞、脂肪细胞、周细胞或星状细胞。这些复杂的起源可能是其功能多样性的基础,其功能多样性包括在细胞外基质重塑中的促肿瘤作用、对抗肿瘤免疫的抑制以及对癌症治疗的抗性。最近报道了几种靶向CAFs以抑制肿瘤进展和增强抗肿瘤免疫的方法。虽然临床前研究显示出了前景,但迄今为止,它们在针对黑色素瘤、乳腺癌、胰腺癌和结直肠癌的人体临床试验中均未成功。本综述总结了CAF靶向治疗的最新重大进展,包括基于DNA的疫苗、抗CAF嵌合抗原受体T细胞(CAR-T细胞)以及对CAF功能的修饰和重编程。强调了开发有效的抗CAF治疗所面临的挑战,包括CAF的异质性和可塑性、缺乏CAFs的特异性靶标标记、在重现人类癌症微环境的动物模型中的局限性以及不良的脱靶和全身副作用。克服这些挑战并扩大我们对CAFs基本生物学的理解,对于在针对人类患者癌症的安全有效治疗策略方面取得进展是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59eb/9405783/723a2dc1d1e1/cancers-14-03906-g001.jpg

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