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Extracellular vesicle-mediated crosstalk between pancreatic cancer and stromal cells in the tumor microenvironment

期刊

JOURNAL OF NANOBIOTECHNOLOGY
卷 20, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12951-022-01382-0

关键词

Extracellular vesicles; Pancreatic cancer; Tumor microenvironment; Communication; Clinical applications

资金

  1. National Natural Science Foundation of China [81802888]
  2. Key Technology Research and Development Program of Shandong [2018GSF118088]
  3. China Postdoctoral Science Foundation [2016M592143]

向作者/读者索取更多资源

Pancreatic cancer interacts closely with the tumor microenvironment, and extracellular vesicles play a key role in this interaction. Understanding the selective packaging and mechanistic impact of these vesicles is important for understanding cancer biology. This review summarizes recent findings on the interactions between pancreatic cancer and stromal cells, as well as the mechanisms involved in immune response and chemoresistance. It also identifies extracellular vesicles as potential diagnostic biomarkers and therapeutic targets for pancreatic cancer.
Pancreatic ductal adenocarcinoma (PDAC) interacts closely with the tumor microenvironment (TME). The TME is remodeled by crosstalk between pancreatic cancer cells and stromal cells, and is critical for cancer progression. Extracellular vesicles (EVs), including exosomes and microvesicles, help facilitate an exchange of information both within the TME and to distant organs. EVs have also been identified as potential diagnostic biomarkers, therapeutic targets, and drug carriers for pancreatic cancer treatment. Thus, understanding the selective packaging of EVs cargo and its mechanistic impact will increase our understanding of cancer biology. In this review, we collect and analyze recent findings of the pancreatic cancer-stromal cell interactions mediated by EVs and the mechanisms involved in cancer-related immunity and chemoresistance. These studies demonstrate the vital role of EVs in pancreatic cancer reprogramming and TME remodeling. We also summarize the EVs identified as potential PDAC diagnostic biomarkers and possible therapeutic targets. This greater understanding is a promising avenue for transitioning EVs from bench to bedside.

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