m6Am Methyltransferase PCIF1 Promotes LPP3 Mediated Phosphatidic Acid Metabolism and Renal Cell Carcinoma Progression

N6-methyl-2'-O-methyladenosine (m6Am), occurring adjacent to the 7-methylguanosine (m7G) cap structure and catalyzed by the newly identified writer PCIF1 (phosphorylated CTD interacting factor 1), has been implicated in the pathogenesis of various diseases. However, its involvement in renal cell carcinoma (RCC) remains unexplored. Here, significant upregulation of PCIF1 and m6Am levels in RCC tissues are identified, unveiling their oncogenic roles both in vitro and in vivo. Mechanically, employing m6Am-Exo-Seq, LPP3 (phospholipid phosphatase 3) mRNA is identified as a key downstream target whose translation is enhanced by m6Am modification. Furthermore, LPP3 is revealed as a key regulator of phosphatidic acid metabolism, critical for preventing its accumulation in mitochondria and facilitating mitochondrial fission. Consequently, Inhibition of the PCIF1/LPP3 axis significantly altered mitochondrial morphology and reduced RCC tumor progression. In addition, depletion of PCIF1 sensitizes RCC to sunitinib treatment. This study highlights the intricate interplay between m6Am modification, phosphatidic acid metabolism, and mitochondrial dynamics, offering a promising therapeutic avenue for RCC.

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Publication Details

Journal
Advanced Science
Published
2024-10-18
DOI
https://doi.org/10.1002/advs.202404033
Citations
9
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
2.10

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article

m6Am Methyltransferase PCIF1 Promotes LPP3 Mediated Phosphatidic Acid Metabolism and Renal Cell Carcinoma Progression

Xianjiong Chen, Yi Lu, Yudong Lin, Liqun Xia et al.
9 citations
Advanced Science
RNA modifications and cancer
2.10
article

m6Am Methyltransferase PCIF1 Promotes LPP3 Mediated Phosphatidic Acid Metabolism and Renal Cell Carcinoma Progression

Xianjiong Chen, Yi Lu, Yudong Lin, Liqun Xia, Zeyi Lu, Gonghui Li, Luying Guo, Xudong Mao, Wenqin Luo, Housheng Hansen He, Zhehao Xu, Haiyun Xie, Lifeng Ding, Ziwei Zhu, Fan Li, Yang Li, Ruyue Wang, Xiaojing Yu, Huan Wang
article en
9 citations

Abstract

N6-methyl-2'-O-methyladenosine (m6Am), occurring adjacent to the 7-methylguanosine (m7G) cap structure and catalyzed by the newly identified writer PCIF1 (phosphorylated CTD interacting factor 1), has been implicated in the pathogenesis of various diseases. However, its involvement in renal cell carcinoma (RCC) remains unexplored. Here, significant upregulation of PCIF1 and m6Am levels in RCC tissues are identified, unveiling their oncogenic roles both in vitro and in vivo. Mechanically, employing m6Am-Exo-Seq, LPP3 (phospholipid phosphatase 3) mRNA is identified as a key downstream target whose translation is enhanced by m6Am modification. Furthermore, LPP3 is revealed as a key regulator of phosphatidic acid metabolism, critical for preventing its accumulation in mitochondria and facilitating mitochondrial fission. Consequently, Inhibition of the PCIF1/LPP3 axis significantly altered mitochondrial morphology and reduced RCC tumor progression. In addition, depletion of PCIF1 sensitizes RCC to sunitinib treatment. This study highlights the intricate interplay between m6Am modification, phosphatidic acid metabolism, and mitochondrial dynamics, offering a promising therapeutic avenue for RCC.

Advanced ScienceVol. 11(46)
University Health Network (CA), University of Toronto (CA), Sir Run Run Shaw Hospital (CN), Princess Margaret Cancer Centre (CA), First Affiliated Hospital Zhejiang University (CN), Zhejiang University (CN)
National Natural Science Foundation of China, Zhejiang University, Natural Science Foundation for Young Scientists of Shanxi Province, Young Scientists Fund, Natural Science Foundation of Zhejiang Province
Good health and well-being
Openalex Percentile: Top 12%
RNA modifications and cancer
2.10
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