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mA Methyltransferase KIAA1429 Regulates the Cisplatin Sensitivity of Gastric Cancer Cells via Stabilizing FOXM1 mRNA. | LitMetric

AI Article Synopsis

  • * In experiments, cisplatin-resistant gastric cancer cells exhibited higher levels of KIAA1429 and mRNA modification, and knocking down KIAA1429 improved their sensitivity to cisplatin treatment.
  • * The study revealed that KIAA1429 stabilizes FOXM1 mRNA through interaction with YTHDF1, suggesting that targeting KIAA1429 could enhance cisplatin effectiveness in resistant gastric cancer.

Article Abstract

Although cisplatin is frequently used to treat gastric cancer, the resistance is the main obstacle for effective treatment. mRNA modification, N6-methyladenosine (mA), is involved in the tumorigenesis of many types of cancer. As one of the largest mA methyltransferase complex components, KIAA1429 bridges the catalytic mA methyltransferase components, such as METTL3. In gastric cancer, KIAA1429 was reported to promote cell proliferation. However, whether KIAA1429 is involved in the resistance of gastric cancer to cisplatin remains unclear. Here, we generated cisplatin resistant gastric cancer cell lines, and compared the mA content between resistant cells and wild type cells. The mA content as well as KIAA1429 expression are higher in resistant cells. Interestingly, the expression of KIAA1429 was significantly increased after cisplatin treatment. We then used shRNA to knockdown KIAA1429 and found that resistant cells responded more to cisplatin treatment after KIAA1429 depletion, while overexpression of KIAA1429 decreased the sensitivity. Moreover, we identified a putative p65 binding site on the promoter area of KIAA1429 and ChIP assay confirmed the binding. p65 depletion decreased the expression of KIAA1429. YTHDF1 is the most abundant mA "reader" that interacts with mA modified mRNA. Mechanistically, YTHDF1 was recruited to the 3'-untranslated Region (3'-UTR) of transcriptional factor, FOXM1 by KIAA1429 and stabilized FOXM1 mRNA. More importantly, KIAA1429 knockdown increased the sensitivity of resistant cells to cisplatin in vivo. In conclusion, our results demonstrated that KIAA1429 facilitated cisplatin resistance by stabilizing FOXM1 mRNA in gastric cancer cells.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600291PMC
http://dx.doi.org/10.3390/cancers14205025DOI Listing

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