4.5 Article

DNA methyltransferase 1 is essential for initiation of the colon cancers

期刊

EXPERIMENTAL AND MOLECULAR PATHOLOGY
卷 94, 期 2, 页码 322-329

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.yexmp.2012.10.004

关键词

Cancer stem cell; Colon cancer; DNMT1

资金

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan from the Japan Science and Technology Agency [16209013, 17016061, 15659097]
  2. Ministry of Health, Labor and Welfare of Japan, Ono Cancer Research Fund [15-17, 19-14]
  3. Takeda Science Foundation
  4. National Cancer Center Research and Development Fund [23-A-44]
  5. Grants-in-Aid for Scientific Research [24791467, 24590449, 23501261, 24659165, 23590427, 23659658] Funding Source: KAKEN

向作者/读者索取更多资源

DNA methyltransferase 1 (Dnmt1) is essential for the maintenance of hematopoietic and somatic stem cells in mice; however, its roles in human cancer stem-like cells (CSCs)/cancer-initiating cells (CICs) are still elusive. In the present study, we investigated DNMT1 functions in the maintenance of human colon CSCs/CICs using the human colon cancer cell line HCT116 (HCT116 w/t) and its DNMT1 knockout cell line (DNMT1(-/-)). The rates of CSCs/CICs were evaluated by side population (SP) analysis, ALDEFLUOR assay and expression of CD44 and CD24. SP, ALDEFLUOR-positive (ALDEFLUOR(+)) and CD44-positive and CD24-positive (CD44(+)CD24(+)) cell rates were lower in DNMT1(-/-) cells than in HCT116 w/t cells. Since CSCs/CICs have higher tumor-initiating ability than that of non-CSCs/CICs, the tumor-initiating abilities were addressed by injecting immune deficient (NOD/SCID) mice. DNMT1(-/-) cells showed less tumor-initiating ability than did HCT116 w/t cells, whereas the growing rate of DNMT1(-/-) cells showed no significant difference from that of HCT116 cells both in vitro and in vivo. Similar results were obtained for cells in which DNMT1 had been transiently knocked-down using gene-specific siRNAs. Taken together, these results indicate that DNMT1 is essential for maintenance of colon CSCs/CICs and that short-term suppression of DNMT1 might be sufficient to disrupt CSCs/CICs. (C) 2012 Elsevier Inc. All rights reserved.

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