Evidence map›Paper›PMID 25186085›Full record

ArticleHuman cell2015

Matriptase and MET are prominently expressed at the site of bone metastasis in renal cell carcinoma: immunohistochemical analysis.

Shoichiro Mukai, Kenji Yorita, Yukari Kawagoe, Yuichi Katayama, Kozue Nakahara, Toyoharu Kamibeppu, Satoru Sugie, Hiromasa Tukino, Toshiyuki Kamoto, Hiroaki Kataoka

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Human cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03149822 (Phase I/II Study of Pembrolizumab and Cabozantinib in Patients With Metastatic Renal Cell Carcinoma), which is not on this map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.4field-weighted citation impact, top 18% 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.

NCT03149822 phase1 / phase2completednot on this mapstarted 2017, after this paper: background citation

Phase I/II Study of Pembrolizumab and Cabozantinib in Patients With Metastatic Renal Cell Carcinoma

TypeinterventionalSponsorUniversity of Colorado, DenverRan2017 to 2024Enrolled45ConditionsMetastatic Renal Cell CarcinomaArmsCabozantinib, Pembrolizumab
3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 46 citations in OpenAlex.

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  14. Immuno-PET Detects Changes in Multi-RTK Tumor Cell Expression Levels in Response to Targeted Kinase Inhibition.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2021
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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

10 authors at 1 institution in 1 country.

Shoichiro MukaiDepartment of Urology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan, syoichiro_mukai@med.miyazaki-u.ac.jp.
Kenji Yorita
Yukari Kawagoe
Yuichi Katayama
Kozue Nakahara
Toyoharu Kamibeppu
Satoru Sugie
Hiromasa Tukino
Toshiyuki Kamoto
Hiroaki Kataoka
University of Miyazaki · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High MET expression in renal cell carcinoma (RCC) and MET activation in bone metastases are reportedly important in progression of several cancers. To find new treatment targets in bone metastasis, we immunohistochemically analyzed expression levels of MET and matriptase (specific cellular activator of hepatocyte growth factor). We obtained nephrectomy specimens from 17 RCC patients with metastasis, and bone metastases specimens from 7 RCC patients who underwent metastasectomies, and who were treated at our hospital between 2008 and 2012. We tested the samples with anti-human MET polyclonal antibody and anti-human matriptase polyclonal antibody, and compared postoperative overall survival (OS) rates between positive and negative groups. High MET expression was seen at primary sites in 8/17 (47%) nephrectomy specimens, and 6/7 (86%) bone specimens. Matriptase was expressed in 6/17 (35%) nephrectomy specimens, and all 7 (100%) bone specimens. Interestingly, matriptase was strongly expressed in osteoclasts of 5/7 bone specimens. Postoperative OS rate was significantly higher in the MET(-) group than the MET(+) group. The high MET and matriptase expression seen in RCC cells in bone metastasis accompanied by matriptase expression in osteoclasts indicates their importance in bone metastasis.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedBone NeoplasmsCarcinoma, Renal CellFemaleGene ExpressionHumansImmunohistochemistryKidney NeoplasmsMaleMiddle AgedProto-Oncogene Proteins c-metRetrospective StudiesSerine EndopeptidasesmatriptaseMET protein, humanProto-Oncogene Proteins c-metSerine Endopeptidases

Identifiers

PMID25186085
PMCPMC4286132
OpenAlexW2081476447

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.