Evidence map›Paper›PMID 31645095›Full record

ArticleCancer research and treatment2020

Prevalence and Clinicopathological Significance of MET Overexpression and Gene Amplification in Patients with Gallbladder Carcinoma.

Yeseul Kim, Seong Sik Bang, Seungyun Jee, Sungeon Park, Su-Jin Shin, Kiseok Jang

Abstract read
In one paragraph

Article in Cancer research and treatment, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Circular RNAs and Cancers.Advances in experimental medicine and biology · 2025
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Overview of current targeted therapy in gallbladder cancer.Signal transduction and targeted therapy · 2020
    Review
  11. Article
  12. Article
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

6 authors.

Yeseul KimDepartment of Pathology, Hanyang University College of Medicine, Seoul, Korea.
Seong Sik BangDepartment of Pathology, Hanyang University College of Medicine, Seoul, Korea.
Seungyun JeeDepartment of Pathology, Hanyang University College of Medicine, Seoul, Korea.
Sungeon ParkDepartment of Pathology, Hanyang University College of Medicine, Seoul, Korea.
Su-Jin ShinDepartment of Pathology, Hanyang University College of Medicine, Seoul, Korea.
Kiseok JangDepartment of Pathology, Hanyang University College of Medicine, Seoul, Korea.

Funding

Ministry of EducationMinistry of Science, ICT and Future PlanningNational Research Foundation of Korea 2015R1C1A1A01056091;2018R1D1A1B07048798
6 · The paper itself

Abstract

purposeMesenchymal epithelial transition (MET) is a proto-oncogene that encodes a heterodimeric transmembrane receptor tyrosine kinase for the hepatocyte growth factor. Aberrant MET signaling has been described in several solid tumors-especially non-small cell lung cancer- and is associated with tumor progression and adverse prognosis. As MET is a potential therapeutic target, information regarding its prevalence and clinicopathological relevance is crucial. MATERIALS AND

methodsWe investigated MET expression and gene amplification in 113 gallbladder cancers using tissue microarray. Immunohistochemistry was used to evaluate MET overexpression, and silver/fluorescence in situ hybridization (ISH) was used to assess gene copy number.

resultsMET overexpression was found in 37 cases of gallbladder carcinoma (39.8%), and gene amplification was present in 17 cases (18.3%). MET protein expression did not correlate with MET amplification. MET amplification was significantly associated with aggressive clinicopathological features, including high histological grade, advanced pT category, lymph node metastasis, and advanced American Joint Committee on Cancer stage. There was no significant correlation between any clinicopathological factors and MET overexpression. No difference in survival was found with respect to MET overexpression and amplification status.

conclusionOur data suggested that MET might be a potential therapeutic target for targeted therapy in gallbladder cancer, because MET amplification was found in a subset of tumors associated with adverse prognostic factors. Detection of MET amplification by ISH might be a useful predictive biomarker test for anti-MET therapy.

Indexed as

AdultAgedAged, 80 and overFemaleGallbladder NeoplasmsGene AmplificationHumansMaleMiddle AgedPrevalenceProto-Oncogene MasProto-Oncogene Proteins c-metMAS1 protein, humanMET protein, humanProto-Oncogene MasProto-Oncogene Proteins c-metGallbladder cancerGene amplificationGene copy numberImmunohistochemistryIn situ hybridizationMET

Identifiers

PMID31645095
PMCPMC7176974

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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.