Cancer-associated fibroblasts and the tumor microenvironment in non-small cell lung cancer

被引:13
作者
Suzuki, Jun [1 ,2 ]
Tsuboi, Masahiro [1 ]
Ishii, Genichiro [2 ]
机构
[1] Natl Canc Ctr Hosp East, Dept Thorac Surg, 6-5-1 Kashiwanoha, Kashiwa, Chiba 2778577, Japan
[2] Natl Canc Ctr Hosp East, Dept Pathol & Clin Labs, Kashiwa, Chiba, Japan
关键词
Non-small cell lung cancer; stroma; cancer-associated fibroblast; microenvironment; immune microenvironment; tumor-infiltrating lymphocytes; tumor-associated macrophages; drug resistance; EPITHELIAL-MESENCHYMAL TRANSITION; STROMAL FIBROBLASTS; BREAST-CANCER; TGF-BETA; PHASE-I; COLORECTAL-CANCER; DOSE-ESCALATION; POOR-PROGNOSIS; COLON-CANCER; DOUBLE-BLIND;
D O I
10.1080/14737140.2022.2019018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Non-small cell lung cancer (NSCLC) has a markedly poor prognosis as it progresses, and the prognosis is still unsatisfactory even with modern treatments. Cancer is composed of not only cancer cells, but also stroma consisting of various cell types. Cancer-associated fibroblasts (CAFs) are a major component of the stroma and the associated tumor microenvironment (TME). Particularly, CAFs are a critical component in elucidating the biological mechanisms of cancer progression and new therapeutic targets. This article outlines the TME formed by CAFs in NSCLC. Areas covered Focusing on the TME in NSCLC, we discuss the mechanisms by which CAFs are involved in cancer progression, drug resistance, and the development of therapies targeting CAFs. Expert opinion In the TME, CAFs profoundly contribute to tumor progression by interacting with cancer cells through direct contact or paracrine cytokine signaling. CAFs also interact with various other stromal components to establish a tumor-promoting immunosuppressive microenvironment and remodel the extracellular matrix. Furthermore, these effects are closely associated with drug resistance. Further elucidation of the stromal microenvironment, including CAFs, could prove to be crucial in the treatment of NSCLC.
引用
收藏
页码:169 / 182
页数:14
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