Cancer-Associated Fibroblasts in Esophageal Cancer

被引:2
|
作者
Dunbar, Karen J. [1 ]
Wong, Kwok K. [2 ]
Rustgi, Anil K. [1 ,3 ]
机构
[1] Columbia Univ, Irving Med Ctr, Dept Med,Herbert Irving Comprehens Canc Ctr, Div Digest & Liver Dis,Vagelos Coll Phys & Surg, New York, NY 10032 USA
[2] New York Univ Langone Hlth, Perlmutter Canc Ctr, Div Hematol Oncol, New York, NY USA
[3] Irving Canc Res Ctr, Herbert Irving Comprehens Canc Ctr, Room 201,1130 St Nicholas Ave, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
Esophageal Cancer; Cancer-Associated Fibroblasts; Tumor Stroma; Barrett's Esophagus; Squamous Dysplasia; SQUAMOUS-CELL CARCINOMA; CISPLATIN RESISTANCE; TUMOR; MYOFIBROBLASTS; ADENOCARCINOMA; PROGRESSION; LANDSCAPE; SURVIVAL;
D O I
10.1016/j.jcmgh.2024.01.008
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Cancer -associated fibroblasts (CAFs), a heterogenous population, can promote cancer cell proliferation, migration, invasion, immunosuppression, and therapeutic resistance in solid tumors. These effects are mediated through secretion of cytokines and growth factors, remodeling of the extracellular matrix, and providing metabolic support for cancer cells. The presence of CAFs in esophageal carcinoma are associated with reduced overall survival and increased resistance to chemotherapy and radiotherapy; thus, identifying therapeutic vulnerabilities of CAFs is a necessity. In esophageal cancer, the mechanisms for CAF recruitment, CAF -mediated promotion of tumorigenesis, metastatic dissemination, and therapeutic resistance have yet to be fully evaluated. Here, we provide an overview of the current understanding of CAFs in esophageal cancer, namely in esophageal squamous cell carcinoma and esophageal adenocarcinoma, as well as in the preneoplastic conditions that predispose to these cancers. Interestingly, there is a discrepancy in our knowledge of CAF biology between esophageal cancer subtypes, with very few studies in esophageal adenocarcinoma, and its precursor lesion Barrett's esophagus, compared with esophageal squamous cell carcinoma. We propose that although great strides have been made, certain questions remain to which answers hopefully will emerge to have an impact on biomarker diagnostics and translational therapeutics. (Cell Mol Gastroenterol Hepatol 2024;17:687-695; https:// doi.org/10.1016/j.jcmgh.2024.01.008)
引用
收藏
页码:687 / 695
页数:9
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