松隈 聰
Affiliate Master
Yamaguchi University
An invited review following the Soujinkai Young Investigator Award : calreticulin is highly expressed in pancreatic cancer stem-like cells
The bulletin of the Yamaguchi Medical School Volume 67 Issue 3-4
Page 19-23
published_at 2020
Title
An invited review following the Soujinkai Young Investigator Award : calreticulin is highly expressed in pancreatic cancer stem-like cells
Creators
Yoshimura Kiyoshi
Source Identifiers
Creator Keywords
pancreatic cancer
cancer stem-like cells
calreticulin
Pancreatic cancer is an intractable disease with a poor prognosis. Recent research has demonstrated that the resistance of these cancers to conventional treatment, the high rate of local recurrence and distant metastasis may be attributed to a small subset of cells in cancer tissues known as cancer stem-like cells. It is critically important to elucidate the biological properties of cancer stem-like cells and develop strategies targeting these cells to overcome pancreatic cancers. We established a pancreatic cancer stem-like cell induction method from a cancer cell line and identified calreticulin as a highly expressed protein on the surface of these cells using proteomics and flow cytometry. Notably, we demonstrated that calreticulin was expressed on cells with high ATP-binding cassette transporter activity known to mediate drug efflux and related to poor outcomes in pancreatic cancer patients who underwent curative resection. Calreticulin exposure in cancer stem-like cells could be regulated by oxidative stress via hypoxia-inducible factors which induce the expression of CD47 and PD-L1 to evade the immune-surveillance of these cells. Further investigations on calreticulin expression in pancreatic cancer stem-like cells could elucidate the pathophysiology of these cells, leading to the development of novel therapy.
Languages
eng
Resource Type
departmental bulletin paper
Publishers
Yamaguchi University School of Medicine
Date Issued
2020
File Version
Version of Record
Access Rights
open access
Relations
[ISSN]0513-1812
[NCID]AA00594272