Pancreatic stellate cell: Update on molecular investigations and clinical translation in pancreatic cancer

被引:0
|
作者
Liu, Yawei [1 ,2 ]
Xue, Ran [3 ]
机构
[1] Capital Med Univ, Sch Basic Med Sci, Beijing, Peoples R China
[2] Capital Med Univ, Beijing Luhe Hosp, Beijing, Peoples R China
[3] Peking Univ Canc Hosp & Inst, Minist Educ Beijing, Dept Early Drug Dev Ctr, Key Lab Carcinogenesis & Translat Res, Fucheng Rd 52, Beijing 100142, Peoples R China
基金
中国国家自然科学基金;
关键词
pancreatic stellate cells; therapeutic strategy; tumor-stromal crosstalk; ACINAR-CELLS; MEDIATED ACTIVATION; FLUFENAMIC ACID; ION CHANNELS; PROMOTE; GROWTH; MICROENVIRONMENT; STIMULATION; INHIBITION; AUTOPHAGY;
D O I
10.1002/ijc.35326
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pancreatic cancer is a particularly aggressive tumor, distinguished by the presence of a prominent collagenous stroma and desmoplasia that envelops the tumor cells. Pancreatic stellate cell (PSC) contributes to the formation of a dense fibrotic stroma and has been demonstrated to facilitate tumor progression. As the significance of PSCs is increasingly revealed, more explorations are focused on the complex molecular mechanisms and tumor-stromal crosstalk in order to guide potential therapeutic approaches through deactivating or reprogramming PSCs. Nevertheless, significant challenges persist in translating preclinical discoveries into clinical applications. In this review, we expect to offer a comprehensive overview of the latest molecular advancements in PSCs, along with new insights into the clinical therapeutic strategies targeting PSCs.
引用
收藏
页数:14
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