Evidence map›Paper›PMID 38402202›Full record

ArticleCell death & disease2024

PRMT1-mediated PGK1 arginine methylation promotes colorectal cancer glycolysis and tumorigenesis.

Hao Liu, Xintian Chen, Pengfei Wang, Miaolei Chen, Chuyin Deng, Xingyou Qian, Jin Bai, Zhongwei Li, Xiangyang Yu

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
11.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 49 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 6 institutions in 1 country.

Hao Liu *School of Medicine, Nankai University, Tianjin, China.
Xintian Chen *Department of Gastroenterology, the Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong, China.
Pengfei WangDepartment of Gastroenterology, the First People's Hospital of Shuyang County, Suqian, Jiangsu, China.
Miaolei ChenCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Chuyin DengCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Xingyou QianCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Jin BaiCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China. bj@xzhmu.edu.cn.ORCID 0000-0003-1524-7893
Zhongwei LiCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China. lizw074@xzhmu.edu.cn.ORCID 0000-0003-1014-4238
Xiangyang YuSchool of Medicine, Nankai University, Tianjin, China. yxynankai@126.com.
Xuzhou Medical College · CNGuangdong Medical College · CNJiangsu University · CNNankai University · CNThe First People's Hospital of Guiyang · CNWannan Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many types of cancer cells, including colorectal cancer cells (CRC), can simultaneously enhance glycolysis and repress the mitochondrial tricarboxylic acid (TCA) cycle, which is called the Warburg effect. However, the detailed mechanisms of abnormal activation of the glycolysis pathway in colorectal cancer are largely unknown. In this study, we reveal that the protein arginine methyltransferase 1 (PRMT1) promotes glycolysis, proliferation, and tumorigenesis in CRC cells. Mechanistically, PRMT1-mediated arginine asymmetric dimethylation modification of phosphoglycerate kinase 1 (PGK1, the first ATP-producing enzyme in glycolysis) at R206 (meR206-PGK1) enhances the phosphorylation level of PGK1 at S203 (pS203-PGK1), which inhibits mitochondrial function and promotes glycolysis. We found that PRMT1 and meR206-PGK1 expression were positively correlated with pS203-PGK1 expression in tissues from colorectal cancer patients. Furthermore, we also confirmed that meR206-PGK1 expression is positively correlated with the poor survival of patients with colorectal cancer. Our findings show that PRMT1 and meR206-PGK1 may become promising predictive biomarkers for the prognosis of patients with CRC and that arginine methyltransferase inhibitors have great potential in colorectal cancer treatment.

Indexed as

Colorectal NeoplasmsPhosphoglycerate KinaseArginineCarcinogenesisCell Line, TumorCell Transformation, NeoplasticGlycolysisHumansMethylationProtein-Arginine N-MethyltransferasesRepressor ProteinsArgininePGK1 protein, humanPhosphoglycerate KinasePRMT1 protein, humanProtein-Arginine N-MethyltransferasesRepressor Proteins

Identifiers

PMID38402202
PMCPMC10894231
OpenAlexW4392133089

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.