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Mist1 Expressing Gastric Stem Cells Maintain the Normal and Neoplastic Gastric Epithelium and Are Supported by a Perivascular Stem Cell Niche
Y. Hayakawa, H. Ariyama, J. Stancikova, K. Sakitani, S. Asfaha, BW. Renz, ZA. Dubeykovskaya, W. Shibata, H. Wang, CB. Westphalen, X. Chen, Y. Takemoto, W. Kim, SS. Khurana, Y. Tailor, K. Nagar, H. Tomita, A. Hara, AR. Sepulveda, W. Setlik, MD....
Language English Country United States
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
NLK
Cell Press Free Archives
from 2002-02-01 to 1 year ago
Free Medical Journals
from 2002 to 1 year ago
- MeSH
- Anoikis MeSH
- Cell Lineage MeSH
- Time Factors MeSH
- Chemokine CXCL12 metabolism MeSH
- Endothelial Cells metabolism pathology MeSH
- Epithelial Cells drug effects metabolism pathology MeSH
- Cadherins metabolism MeSH
- Humans MeSH
- Lymphocytes metabolism pathology MeSH
- Cell Communication MeSH
- Mice, Transgenic MeSH
- Mice MeSH
- Cell Transformation, Neoplastic genetics metabolism pathology MeSH
- Cell Line, Tumor MeSH
- Neoplastic Stem Cells drug effects metabolism pathology MeSH
- Tumor Microenvironment * MeSH
- Stomach Neoplasms drug therapy genetics metabolism pathology MeSH
- Stem Cell Niche * MeSH
- Wnt Proteins metabolism MeSH
- Antineoplastic Agents pharmacology MeSH
- Receptors, CXCR4 metabolism MeSH
- rho GTP-Binding Proteins metabolism MeSH
- Wnt Signaling Pathway MeSH
- Signal Transduction MeSH
- Cellular Senescence MeSH
- Basic Helix-Loop-Helix Transcription Factors genetics metabolism MeSH
- Bone Marrow Transplantation MeSH
- Gastric Mucosa drug effects metabolism pathology MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
The regulation and stem cell origin of normal and neoplastic gastric glands are uncertain. Here, we show that Mist1 expression marks quiescent stem cells in the gastric corpus isthmus. Mist1(+) stem cells serve as a cell-of-origin for intestinal-type cancer with the combination of Kras and Apc mutation and for diffuse-type cancer with the loss of E-cadherin. Diffuse-type cancer development is dependent on inflammation mediated by Cxcl12(+) endothelial cells and Cxcr4(+) gastric innate lymphoid cells (ILCs). These cells form the perivascular gastric stem cell niche, and Wnt5a produced from ILCs activates RhoA to inhibit anoikis in the E-cadherin-depleted cells. Targeting Cxcr4, ILCs, or Wnt5a inhibits diffuse-type gastric carcinogenesis, providing targets within the neoplastic gastric stem cell niche.
Department of Radiation Oncology Albert Einstein College of Medicine Bronx NY 10461 USA
Department of Tumor Pathology Gifu University Graduate School of Medicine Gifu 501 1194 Japan
Division of Comparative Medicine Massachusetts Institute of Technology Cambridge MA 02139 USA
References provided by Crossref.org
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