Evidence map›Paper›PMID 34145400›Full record

ReviewOncogene2021

HGF/c-MET pathway in cancer: from molecular characterization to clinical evidence.

Jianjiang Fu, Xiaorui Su, Zhihua Li, Ling Deng, Xiawei Liu, Xuancheng Feng, Juan Peng

Abstract readReview
PubMed Publisher
In one paragraph

Review in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 121 papers.

0numbers the graph read from it
0cells of the map it votes in
121citing papers in PubMed
17.3field-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

121 citing papers in PubMed, 210 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Paclitaxel drives TREM2Nature communications · 2026
    Article
  15. Article
  16. Article
  17. Review
  18. Native Ligand-Inspired peptides for c-MET targeted PET probes development.European journal of nuclear medicine and molecular imaging · 2025
    Article
  19. Article
  20. Article

61 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

7 authors at 3 institutions in 1 country.

Jianjiang Fu *Department of Pathology, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.ORCID 0000-0002-3952-9898
Xiaorui Su *Department of Pathology, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.ORCID 0000-0001-5847-1794
Zhihua Li *The Third Clinical School of Guangzhou Medical University, Guangzhou, China.ORCID 0000-0003-0840-749X
Ling DengDepartment of Molecular Diagnostics, Sun Yat-sen University Cancer Center, Guangzhou, China.ORCID 0000-0002-3195-3088
Xiawei LiuDepartment of Pathology, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.ORCID 0000-0001-9508-1832
Xuancheng FengDepartment of Pathology, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China. 2816924339@qq.com.ORCID 0000-0002-8722-6306
Juan PengDepartment of Pathology, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China. pengjuan1979@yahoo.com.ORCID 0000-0001-6308-3040
Guangdong University of Education · CNThird Affiliated Hospital of Guangzhou Medical University · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This review provides a comprehensive landscape of HGF/c-MET (hepatocyte growth factor (HGF) /mesenchymal-epithelial transition factor (c-MET)) signaling pathway in cancers. First, we generalize the compelling influence of HGF/c-MET pathway on multiple cellular processes. Then, we present the genomic characterization of HGF/c-MET pathway in carcinogenesis. Furthermore, we extensively illustrate the malignant biological behaviors of HGF/c-MET pathway in cancers, in which hyperactive HGF/c-MET signaling is considered as a hallmark. In addition, we investigate the current clinical trials of HGF/c-MET-targeted therapy in cancers. We find that although HGF/c-MET-targeted therapy has led to breakthroughs in certain cancers, monotherapy of targeting HGF/c-MET has failed to demonstrate significant clinical efficacy in most cancers. With the advantage of the combinations of HGF/c-MET-targeted therapy, the exploration of more options of combinational targeted therapy in cancers may be the major challenge in the future.

Indexed as

Hepatocyte Growth FactorNeoplasmsProto-Oncogene Proteins c-metSignal TransductionAnimalsHumansMolecular Targeted TherapyHepatocyte Growth FactorHGF protein, humanMET protein, humanProto-Oncogene Proteins c-met

Identifiers

PMID34145400
OpenAlexW3171106033

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.