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Cancer-associated fibroblasts mediate resistance to anti-EGFR therapies in cancer.
Dai, Shuang; Liu, Yingtong; Liu, Zheran; Li, Ruidan; Luo, Feng; Li, Yan; Dai, Lei; Peng, Xingchen.
  • Dai S; Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China; Lung Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
  • Liu Y; Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China; Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan 610041, China.
  • Liu Z; Department of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu Sichuan, China.
  • Li R; Department of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu Sichuan, China.
  • Luo F; Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China; Lung Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
  • Li Y; Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China; Lung Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China. Electronic address: liyan1240@wchscu.cn.
  • Dai L; State Key Laboratory of Biotherapy/Collaborative Innovation Center for Biotherapy, West China Hospital, Sichuan University, Chengdu, Sichuan, China. Electronic address: daileisklb2012@163.com.
  • Peng X; Department of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu Sichuan, China. Electronic address: pxx2014@163.com.
Pharmacol Res ; 206: 107304, 2024 Aug.
Article en En | MEDLINE | ID: mdl-39002870
ABSTRACT
Over the last decade, epidermal growth factor receptor (EGFR)-targeted therapies have transformed the treatment landscape for patients with advanced solid tumors. Despite these advances, resistance to anti-EGFR therapies is still a significant clinical challenge. While cell-autonomous mechanisms of resistance are well-documented, they do not fully elucidate the complexity of drug resistance. Cancer-associated fibroblasts (CAFs), key mediators within the tumor microenvironment (TME), have emerged as pivotal players in cancer progression and chemoresistance. Recent evidence implicates CAFs in resistance to anti-EGFR therapies, suggesting they may undermine treatment efficacy. This review synthesizes current data, highlighting the critical role of CAFs in resistance pathogenesis and summarizing recent therapeutic strategies targeting CAFs. We underscore the challenges and advocate for the exploration of CAFs as a potential dual-targeted approach.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Resistencia a Antineoplásicos / Microambiente Tumoral / Receptores ErbB / Fibroblastos Asociados al Cáncer / Neoplasias / Antineoplásicos Límite: Animals / Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Resistencia a Antineoplásicos / Microambiente Tumoral / Receptores ErbB / Fibroblastos Asociados al Cáncer / Neoplasias / Antineoplásicos Límite: Animals / Humans Idioma: En Año: 2024 Tipo del documento: Article