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Volume 52 Issue 8
Aug.  2025
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Article Contents

Vitamin D receptor regulates methyltransferase like 14 to mitigate colitis-associated colorectal cancer

doi: 10.1016/j.jgg.2024.12.020
Funds:

The Integrated Entrusted Project of Research Funding at Peking Union Medical College Hospital (ZC201903347)

CAMS Innovation Fund for Medical Sciences (2021-I2M-1-001)

Health Research &

We thank the Pathology Department, Biomarker Discovery and Validation Facility, Laboratory Animal Research Facility of Institute of Clinical Medicine of PUMCH for supporting this study. We sincerely thank Prof. Tong and the members of the Department of Pathology at the Center for Experimental Animal Research, Institute of Basic Medical Sciences, PUMC. This work was funded by National High-Level Hospital Clinical Research Funding (2022-PUMCH-A-203)

Special Projects Grant of China (201002020 and 201502005)

Capital Health Development Scientific Research Fund (2022-2-4014)

the National Natural Science Foundation of China (81970495)

and Peking Union Medical College Hospital Research Funding for Postdoc (kyfyjj202315).

  • Received Date: 2024-07-17
  • Accepted Date: 2024-12-30
  • Rev Recd Date: 2024-12-27
  • Publish Date: 2025-01-06
  • Colitis-associated colorectal cancer (CAC), a serious complication of ulcerative colitis (UC), is associated with a poor prognosis. The vitamin D receptor (VDR) is recognized for its protective role in UC and CAC through the maintenance of intestinal barrier integrity and the regulation of inflammation. This study demonstrates a significant reduction in m6A-related genes, particularly methyltransferase like 14 (METTL14), in UC and CAC patients and identifies an association between METTL14 and VDR. In the azoxymethane (AOM)/dextran sodium sulfate (DSS)-induced mouse model, vitamin D treatment increases METTL14 expression and reduces tumor burden, while Vdr-knockout mice exhibit lower METTL14 levels and increased tumorigenesis. In vitro, the VDR agonist calcipotriol upregulates METTL14 in NCM460 cells, with this effect attenuated by VDR knockdown. VDR knockdown in DLD-1 colon cancer cells decreases METTL14 expression and promotes proliferation, which is reversed by METTL14 overexpression. Mechanistic studies reveal that VDR regulates METTL14 expression via promoter binding, modulating key target genes such as SOX4, DROSH, and PHLPP2. This study highlights the role of the VDR–METTL14 axis as a protective mechanism in CAC and suggests its potential as a therapeutic target for preventing and treating CAC.
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