Evidence map›Paper›PMID 36878949›Full record

ArticleCell death & disease2023

The TRPM7 channel reprograms cellular glycolysis to drive tumorigenesis and angiogenesis.

Wanzhou Wu, Xuan Wang, Longsheng Liao, Jing Chen, Yue Wang, Meilian Yao, Lingping Zhu, Jiayu Li, Xuan Wang, Alex F Chen and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

26 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  6. Article
  7. Role of TRP channels in lymphatic function.Frontiers in physiology · 2026
    Review
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  9. Article
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  17. Unlocking TRPM7 interactions: A database-driven quest.Computational and structural biotechnology journal · 2025
    Review
  18. Review
  19. 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

13 authors at 2 institutions in 1 country.

Wanzhou Wu *Department of Cardiology, The Third Xiangya Hospital, Central South University, Changsha, China.
Xuan Wang *Department of Geriatric Medicine, Xiangya Hospital, Central South University, Changsha, China.
Longsheng LiaoDepartment of Geriatric Medicine, Xiangya Hospital, Central South University, Changsha, China.
Jing ChenDepartment of Geriatric Medicine, Xiangya Hospital, Central South University, Changsha, China.
Yue WangDepartment of Geriatric Medicine, Xiangya Hospital, Central South University, Changsha, China.
Meilian YaoDepartment of Geriatric Medicine, Xiangya Hospital, Central South University, Changsha, China.
Lingping ZhuDepartment of Geriatric Medicine, Xiangya Hospital, Central South University, Changsha, China.
Jiayu LiCollege of Pharmacy, Hunan University of Chinese Medicine, Changsha, China.
Xuan WangDepartment of Pharmacology, Hunan Key Laboratory of Cardiovascular Research, Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, China.
Alex F ChenCenter for Vascular Disease and Translational Medicine, Department of Cardiology, The Third Xiangya Hospital, Central South University, Changsha, China.
Guogang ZhangDepartment of Geriatric Medicine, Xiangya Hospital, Central South University, Changsha, China.
Zheng ZhangDepartment of Pharmacology, Hunan Key Laboratory of Cardiovascular Research, Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, China. zzhang@csu.edu.cn.
Yongping BaiDepartment of Geriatric Medicine, Xiangya Hospital, Central South University, Changsha, China. baiyongping@csu.edu.cn.ORCID 0000-0002-6355-5842
Central South University · CNHunan University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer or endothelial cells preferably catabolize glucose through aerobic glycolysis rather than oxidative phosphorylation. Intracellular ionic signaling has been shown to regulate glucose metabolism, but the underlying ion channel has yet to be identified. RNA-seq, metabolomics and genetic assay revealed that the TRPM7 channel regulated cellular glycolysis. Deletion of TRPM7 suppressed cancer cell glycolysis and reduced the xenograft tumor burden. Deficiency of endothelial TRPM7 inhibited postnatal retinal angiogenesis in mice. Mechanistically, TRPM7 transcriptionally regulated the solute carrier family 2 member 3 (SLC2A3, also known as GLUT3) via Ca

Indexed as

Endothelial CellsTRPM Cation ChannelsAnimalsCalcineurinCarcinogenesisCell Transformation, NeoplasticGlycolysisHumansMiceProtein Serine-Threonine KinasesCalcineurinProtein Serine-Threonine KinasesTRPM7 protein, humanTrpm7 protein, mouseTRPM Cation Channels

Identifiers

PMID36878949
PMCPMC9988972
OpenAlexW4323320073

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.