Evidence map›Paper›PMID 37749229›Full record

ArticleOncogene2023

GPR37 promotes colorectal cancer liver metastases by enhancing the glycolysis and histone lactylation via Hippo pathway.

Jiamin Zhou, Weiqi Xu, Yibin Wu, Miao Wang, Ning Zhang, Longrong Wang, Yun Feng, Ti Zhang, Lu Wang, Anrong Mao

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 110 papers.

0numbers the graph read from it
0cells of the map it votes in
110citing papers in PubMed
24.4field-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

110 citing papers in PubMed, 106 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Research progress of lactylation modification in tumors (Review).Experimental and therapeutic medicine · 2026
    Review
  6. Article
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  8. Review
  9. Review
  10. Article
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  12. Review
  13. Targeting Lactate and Lactylation in Cancer Metabolism and Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  14. Review
  15. Review
  16. Review
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  18. [Research progress on protein lactylation modification in malignant tumors].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2026
    Review
  19. Review
  20. Review

50 more citing papers are in PubMed but not listed here.

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

10 authors at 1 institution in 1 country.

Jiamin Zhou *Department of Hepatic Surgery, Shanghai Cancer Center, Fudan University, Shanghai, 200032, PR China.
Weiqi Xu *Department of Hepatic Surgery, Shanghai Cancer Center, Fudan University, Shanghai, 200032, PR China.ORCID 0000-0002-5861-9389
Yibin Wu *Department of Hepatic Surgery, Shanghai Cancer Center, Fudan University, Shanghai, 200032, PR China.
Miao WangDepartment of Hepatic Surgery, Shanghai Cancer Center, Fudan University, Shanghai, 200032, PR China.
Ning ZhangDepartment of Hepatic Surgery, Shanghai Cancer Center, Fudan University, Shanghai, 200032, PR China.
Longrong WangDepartment of Hepatic Surgery, Shanghai Cancer Center, Fudan University, Shanghai, 200032, PR China.
Yun FengDepartment of Hepatic Surgery, Shanghai Cancer Center, Fudan University, Shanghai, 200032, PR China.
Ti ZhangDepartment of Hepatic Surgery, Shanghai Cancer Center, Fudan University, Shanghai, 200032, PR China.
Lu WangDepartment of Hepatic Surgery, Shanghai Cancer Center, Fudan University, Shanghai, 200032, PR China. wangluzl@fudan.edu.cn.ORCID 0000-0002-6856-7084
Anrong MaoDepartment of Hepatic Surgery, Shanghai Cancer Center, Fudan University, Shanghai, 200032, PR China. 13020143060@163.com.ORCID 0000-0002-4596-508X
Shanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver metastases are commonly detected in a range of malignancies including colorectal cancer (CRC), unfortunately no effectively strategies for CRC liver metastasis (CRLM). In this study, we found GPR37 expression dramatically increased in human CRLM specimens and associated poor prognosis. GPR37 depletion greatly suppressed the liver metastasis in the mouse models of CRLM. Functional experiments showed that GPR37 knockdown inhibited the growth by reducing the glycolysis of CRC cells. Also, GPR37 knockdown in tumor cells produced decreased levels of two chemokines involved in neutrophil accumulation, which abrogated neutrophil recruitment in the tumor microenvironment of CRLM. Finally, the mechanism studies revealed that GPR37 could activate the hippo pathway, thereby promoting LDHA expression and glycolysis. This leads to increased lactylation of H3K18la, resulting in up-regulation of CXCL1 and CXCL5. These results support a role of the GPR37 in modulating the tumor metabolism and microenvironment in CRLM and GPR37 could be a potential therapeutic target.

Indexed as

Colorectal NeoplasmsLiver NeoplasmsAnimalsGlycolysisHippo Signaling PathwayHistonesHumansMiceReceptors, G-Protein-CoupledTumor MicroenvironmentGpr37 protein, mouseGPR37 receptor, humanHistonesReceptors, G-Protein-Coupled

Identifiers

PMID37749229
OpenAlexW4387016121

What OpenQuestion holds

Textmetadata
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.