Evidence map›Paper›PMID 36401967›Full record

ArticleTranslational oncology2023

LCMT1 indicates poor prognosis and is essential for cell proliferation in hepatocellular carcinoma.

Ning Zhang, Cailing Lu, Jiao Mo, Xinhang Wang, Simi Liao, Ningjing Liang, Mei Feng, Tingting Tang, Yijie Wu, Yunqing Li and 9 more

Abstract read
In one paragraph

Article in Translational oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
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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

19 authors.

Ning ZhangSchool of Public Health, Guangxi Medical University, Nanning, China; Guangxi Colleges and University Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, China.
Cailing LuSchool of Public Health, Guangxi Medical University, Nanning, China; Guangxi Colleges and University Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, China.
Jiao MoSchool of Public Health, Guangxi Medical University, Nanning, China; Guangxi Colleges and University Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, China.
Xinhang WangSchool of Public Health, Guangxi Medical University, Nanning, China; Guangxi Colleges and University Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, China; School of Basic Medical Sciences, Guangxi Medical University, Nanning, China.
Simi LiaoSchool of Public Health, Guangxi Medical University, Nanning, China; Guangxi Colleges and University Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, China.
Ningjing LiangSchool of Public Health, Guangxi Medical University, Nanning, China; Guangxi Colleges and University Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, China.
Mei FengSchool of Basic Medical Sciences, Guangxi Medical University, Nanning, China.
Tingting TangSchool of Public Health, Guangxi Medical University, Nanning, China; Guangxi Colleges and University Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, China.
Yijie WuSchool of Public Health, Guangxi Medical University, Nanning, China; Guangxi Colleges and University Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, China.
Yunqing LiSchool of Public Health, Guangxi Medical University, Nanning, China; Guangxi Colleges and University Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, China.
Chunhua LanSchool of Basic Medical Sciences, Guangxi Medical University, Nanning, China.
Chengying ChenSchool of Basic Medical Sciences, Guangxi Medical University, Nanning, China.
Qianqian ShiSchool of Public Health, Guangxi Medical University, Nanning, China; Guangxi Colleges and University Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, China.
Lancheng WeiSchool of Public Health, Guangxi Medical University, Nanning, China; Guangxi Colleges and University Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, China.
Zhijian ZhengSchool of Public Health, Guangxi Medical University, Nanning, China; Guangxi Colleges and University Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, China.
Yu LeiSchool of Public Health, Guangxi Medical University, Nanning, China; Guangxi Colleges and University Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, China.
Zhiming ZhangGuangxi Medical University Affiliated Tumor Hospital, China.
Shen TangSchool of Basic Medical Sciences, Guangxi Medical University, Nanning, China. Electronic address: 958714333@qq.com.
Xiyi LiSchool of Public Health, Guangxi Medical University, Nanning, China; Guangxi Colleges and University Key Laboratory of Prevention and Control of Highly Prevalent Diseases, Guangxi Medical University, China. Electronic address: xiyi.li2017@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is one of the most malignant type of cancers. Leuci carboxyl methyltransferase 1 (LCMT1) is a protein methyltransferase that plays an improtant regulatory role in both normal and cancer cells. The aim of this study is to evaluate the expression pattern and clinical significance of LCMT1 in HCC.

methodsThe expression pattern and clinical relevance of LCMT1 were determined using the Gene Expression Omnibus (GEO) database, the Cancer Genome Atlas (TCGA) program, and our datasets. Gain-of-function and loss-of-function studies were employed to investigate the cellular functions of LCMT1 in vitro and in vivo. Quantitative real-time polymerase chain reaction (RT-PCR) analysis, western blotting, enzymatic assay, and high-performance liquid chromatography were applied to reveal the underlying molecular functions of LCMT1.

resultsLCMT1 was upregulated in human HCC tissues, which correlated with a "poor" prognosis. The siRNA-mediated knockdown of LCMT1 inhibited glycolysis, promoted mitochondrial dysfunction, and increased intracellular pyruvate levels by upregulating the expression of alani-neglyoxylate and serine-pyruvate aminotransferase (AGXT). The overexpression of LCMT1 showed the opposite results. Silencing LCMT1 inhibited the proliferation of HCC cells in vitro and reduced the growth of tumor xenografts in mice. Mechanistically, the effect of LCMT1 on the proliferation of HCC cells was partially dependent on PP2A.

conclusionsOur data revealed a novel role of LCMT1 in the proliferation of HCC cells. In addition, we provided novel insights into the effects of glycolysis-related pathways on the LCMT1regulated progression of HCC, suggesting LCMT1 as a novel therapeutic target for HCC therapy.

Indexed as

Cell proliferationHepatocellular carcinoma (HCC)Leucine carboxyl methyltransferase 1 (LCMT1)Prognosis

Identifiers

PMID36401967
PMCPMC9673118

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