4.7 Article

METTL13 inhibits progression of clear cell renal cell carcinoma with repression on PI3K/AKT/mTOR/HIF-1α pathway and c-Myc expression

期刊

JOURNAL OF TRANSLATIONAL MEDICINE
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12967-021-02879-2

关键词

METTL13; Clear cell renal cell carcinoma; Proliferation; Migration; Invasion; Epithelial-mesenchymal transition; HIF-1 alpha; C-Myc

资金

  1. Shenyang Plan Project of Science and Technology [F19-112-4-098]
  2. National key R&D plan key research projects of precision medicine [2017YFC0908000]
  3. Shenyang Clinical Medical Research Center [20-204-4-42]
  4. Liaoning Clinical Medical Research Center [[2020] 44]
  5. Natural Science Foundation of Liaoning Province [2019-MS-378]

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The study found that METTL13 is downregulated in ccRCC and is associated with poor prognosis; METTL13 can inhibit the growth and metastasis of ccRCC cells through multiple molecular mechanisms.
BackgroundClear cell renal cell carcinoma (ccRCC) is the most common and aggressive type of renal malignancy. Methyltransferase like 13 (METTL13) functions as an oncogene in most of human cancers, but its function and mechanism in ccRCC remains unreported.MethodsqRT-PCR, western blotting and immunohistochemistry were used to detect METTL13's expression in tissues. The effects of METTL13 on ccRCC cells' growth and metastasis were determined by both functional experiments and animal experiments. Weighted gene co-expression network analysis (WGCNA) was performed to annotate METTL13's functions and co-immunoprecipitation (co-IP) was used to determine the interaction between METTL13 and c-Myc.ResultsMETTL13 was underexpressed in ccRCC tissues compared to normal kidney tissues and its low expression predicted poor prognosis for ccRCC patients. The in vitro studies showed that knockdown and overexpression of METTL13 respectively led to increase and decrease in ccRCC cells' proliferation, viability, migratory ability and invasiveness as well as epithelial-mesenchymal transition (EMT). The in vivo experiment demonstrated the inhibitory effect that METTL13 had on ccRCC cells' growth and metastasis. Bioinformatic analyses showed various biological functions and pathways METTL13 was involved in. In ccRCC cells, we observed that METTL13 could negatively regulate PI3K/AKT/mTOR/HIF-1 alpha pathway and that it combined to c-Myc and inhibited c-Myc protein expression.ConclusionsIn general, our finding suggests that high expression of METTL13 is associated with favorable prognosis of ccRCC patients. Meanwhile, METTL13 can inhibit growth and metastasis of ccRCC cells with participation in multiple potential molecular mechanisms. Therefore, we suggest METTL13 can be a new diagnostic and therapeutic target for ccRCC in the future.

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