TTC7B triggers the PI4KA-AKT1-RXRA-FTO axis and inhibits colon cancer cell proliferation by increasing RNA

Qianwen Ren1, Meiyi Xiang1, Juanli Qiao1

  • 1Key Laboratory of Carcinogenesis and Translational Research (MOE/Beijing), Division of Etiology, Peking University Cancer Hospital and Institute, Beijing, 100142, China.

Insights

Tetratricopeptide repeat domain 7B (TTC7B) protein binds PI4KA and inhibits colon cancer progression by regulating RNA N6-adenine (m6A) methylation through the RXRA-FTO axis.

Area of Science:

  • Molecular Biology
  • Cancer Research
  • Epigenetics

Background:

  • The upstream regulatory network of RNA N6-adenine (m6A) methylation is not fully understood.
  • Expression of TTC7B, PI4KA, and FTO genes are correlated and downregulated in many cancers.

Purpose of the Study:

  • To elucidate the role of TTC7B in the regulation of RNA m6A methylation and its impact on colon cancer.
  • To investigate the molecular mechanism by which TTC7B affects colon cancer progression.

Main Methods:

  • Bioinformatics analysis of gene expression data.
  • Correlation analysis in human tissues and colon cancer patient samples (n=105).
  • In vitro and in vivo experiments involving gene manipulation and functional assays.

Main Results:

  • TTC7B expression is positively correlated with PI4KA and FTO, and its downregulation is linked to poor prognosis in colon cancer.
  • TTC7B upregulates RXRA via the PI4KA-AKT1 pathway, and RXRA acts as a transcription factor for FTO.
  • TTC7B inhibits colon cancer cell proliferation by increasing FTO expression, reducing RNA m6A levels, an effect dependent on FTO demethylase activity.

Conclusions:

  • TTC7B initiates the RXRA-FTO axis through PI4KA binding, decreasing RNA m6A modification and inhibiting colon cancer progression.
  • This study reveals a novel regulatory pathway for RNA m6A methylation in cancer.

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