国际肿瘤学杂志 ›› 2021, Vol. 48 ›› Issue (5): 308-312.doi: 10.3760/cma.j.cn371439-20200528-00059

• 综述 • 上一篇    下一篇

癌相关成纤维细胞的异质性在靶向胰腺癌治疗中的角色

严志颖, 毛逸锋, 朱颖蔚(), 徐克群()   

  1. 南京医科大学附属常州第二人民医院肿瘤科,常州 213003
  • 收稿日期:2020-05-28 修回日期:2020-09-15 出版日期:2021-05-08 发布日期:2021-06-09
  • 通讯作者: 朱颖蔚,徐克群 E-mail:ywzhu@163.com;13775001122@139.com

Role of heterogeneity of cancer-associated fibroblasts in targeted therapy of pancreatic cancer

Yan Zhiying, Mao Yifeng, Zhu Yingwei(), Xu Kequn()   

  1. Department of Oncology, Changzhou Second People's Hospital Affiliated to Nanjing Medical University, Changzhou 213003, China
  • Received:2020-05-28 Revised:2020-09-15 Online:2021-05-08 Published:2021-06-09
  • Contact: Zhu Yingwei,Xu Kequn E-mail:ywzhu@163.com;13775001122@139.com

摘要:

胰腺癌发病率逐年增高,但临床诊治进展有限,预后差。胰腺癌中肿瘤微环境(TME)与肿瘤侵袭转移和化疗耐药密切相关。癌相关成纤维细胞(CAF)是一种处于持续活化状态的成纤维细胞,是TME中最重要的细胞成分之一。CAF可通过多种分子介导的多种机制,促进胰腺癌的恶性生物学行为。而靶向CAF治疗胰腺癌疗效不佳,可能与胰腺癌中CAF存在异质性有关。故对其异质性深入研究,并以此为基础精确靶向基质中某些特定表型和功能的CAF亚型,在胰腺癌的临床治疗中可能更具有前景。

关键词: 癌相关成纤维细胞, 肿瘤微环境, 分子靶向治疗, 胰腺肿瘤

Abstract:

The incidence of pancreatic cancer is increasing year by year, but the clinical diagnosis and treatment progress is limited and the prognosis is poor. Tumor microenvironment (TME) is closely related to the invasion, metastasis and chemotherapy resistance of pancreatic cancer. Cancer-associated fibroblasts (CAFs) are fibroblasts in a state of continuous activation, which are the most prominent components in TME. CAFs can promote the malignant biological behavior of pancreatic cancer through a variety of molecule-mediated mechanisms. Moreover, several attempts targeting CAFs for the treatment of pancreatic cancer have been largely unsuccessful. It may be related to the heterogeneity of CAFs in pancreatic cancer. Therefore, in-depth study of its heterogeneity and accurate targeting of some specific phenotypes and functional CAFs subtypes in the matrix on this basis may be more promising in the clinical treatment of pancreatic cancer.

Key words: Cancer-associated fibroblasts, Tumor microenvironment, Molecular targeted therapy, Pancreatic neoplasms