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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.
Abstract:
TTC7B is the PI4KA-binding protein. The upstream regulatory network associated with the expression of genes involved in RNA N6-adenine (m6A) methylation is not clear. Bioinformatics analysis revealed that the expression levels of TTC7B, PI4KA, and FTO are positively correlated with each other across human tissues. These genes are consistently downregulated in many cancers. We initially confirmed the correlation of the expression of these genes in colon cancer tissues from patients (n=105) and reported that TTC7B downregulation was significantly associated with poor prognosis. We subsequently performed a series of biological experiments and demonstrated that TTC7B upregulated RXRA expression probably through the PI4KA-mediated AKT1 pathway and that RXRA was a transcription factor for the FTO gene. TTC7B inhibited the proliferation of colon cancer cells by increasing the recruitment of RXRA to the FTO promoter, increasing FTO expression, and decreasing the total RNA m6A level. Ablation of FTO demethylase activity completely abolished the inhibitory effect of TTC7B on the proliferation of cancer cells in vitro and in vivo. In conclusion, our study demonstrated for the first time that TTC7B triggers the RXRA-FTO axis through PI4KA binding, which leads to a decrease in total RNA m6A modification and the inhibition of colon cancer progression.
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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