Evidence map›Paper›PMID 26636767›Full record

ArticlePloS one2015

Relationships between Chromosome 7 Gain, MET Gene Copy Number Increase and MET Protein Overexpression in Chinese Papillary Renal Cell Carcinoma Patients.

Xiaolu Yin, Tianwei Zhang, Xinying Su, Yan Ji, Peng Ye, Haihua Fu, Shuqiong Fan, Yanying Shen, Paul R Gavine, Yi Gu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  9. MET alterations in biphasic squamoid alveolar papillary renal cell carcinomas and clinicopathological features.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
    Article
  10. Review
  11. Review
  12. Article
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  14. High fidelity of driver chromosomal alterations among primary and metastatic renal cell carcinomas: implications for tumor clonal evolution and treatment.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2016
    Article
  15. Review
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 2 institutions in 1 country.

Xiaolu YinAsia & Emerging Markets iMed, AstraZeneca R&D, Shanghai, China.
Tianwei ZhangAsia & Emerging Markets iMed, AstraZeneca R&D, Shanghai, China.
Xinying SuAsia & Emerging Markets iMed, AstraZeneca R&D, Shanghai, China.
Yan JiResearch & Development Information, AstraZeneca R&D, Shanghai, China.
Peng YeAsia & Emerging Markets iMed, AstraZeneca R&D, Shanghai, China.
Haihua FuAsia & Emerging Markets iMed, AstraZeneca R&D, Shanghai, China.
Shuqiong FanAsia & Emerging Markets iMed, AstraZeneca R&D, Shanghai, China.
Yanying ShenDepartment of Pathology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Paul R GavineAsia & Emerging Markets iMed, AstraZeneca R&D, Shanghai, China.
Yi GuAsia & Emerging Markets iMed, AstraZeneca R&D, Shanghai, China.
Renji Hospital · CNShanghai Medical Information Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To investigate the relationships between Chromosome 7 gain, mesenchymal-epithelial transition factor (MET) gene copy number increase and MET protein overexpression in Chinese patients with papillary renal cell carcinoma (PRCC), immunohistochemistry (IHC), immunofluorescence (IF) and fluorescence in situ hybridization (FISH) were performed on 98 formalin-fixed, paraffin-embedded (FFPE) PRCC samples. Correlations between MET gene copy number increase, Chromosome 7 gain and MET protein overexpression were analyzed statistically. A highly significant correlation was observed between the percentage of tumor cells with MET gene copy number ≥3 and CEP7 copy number ≥3 (R2 = 0.90, p<0.001) across two subtypes of PRCC. In addition, the percentage of tumor cells with MET gene copy number ≥3 was found to increase along with increases in MET IHC score. This correlation was further confirmed in those PRCC tumor cells with average MET gene copy number >5 using combined IF and FISH methodology. Overall, this study provides evidence that Chromosome 7 gain drives MET gene copy number increase in PRCC tumors, and appears to subsequently lead to an increase in MET protein overexpression in these tumor cells. This supports MET activation as a potential therapeutic target in sporadic PRCC.

Indexed as

Gene AmplificationAsian PeopleCarcinoma, Renal CellChinaChromosomes, Human, Pair 7FemaleGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseHumansIn Situ Hybridization, FluorescenceKidney NeoplasmsMalePrognosisProto-Oncogene Proteins c-metUp-RegulationMET protein, humanProto-Oncogene Proteins c-met

Identifiers

PMID26636767
PMCPMC4670110
OpenAlexW2193467334

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.