Evidence map›Paper›PMID 28327121›Full record

ArticleBMC urology2017

BAP1 and PBRM1 in metastatic clear cell renal cell carcinoma: tumor heterogeneity and concordance with paired primary tumor.

Jeanette E Eckel-Passow, Daniel J Serie, John C Cheville, Thai H Ho, Payal Kapur, James Brugarolas, R Houston Thompson, Bradley C Leibovich, Eugene D Kwon, Richard W Joseph and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC urology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Determinants of late metastases in renal cell carcinoma.Journal of the National Cancer Institute · 2025
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  18. AJournal of Cancer · 2017
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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

11 authors at 4 institutions in 1 country.

Jeanette E Eckel-PassowDivision of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, USA.
Daniel J SerieDepartment of Health Sciences Research, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 32224, USA.
John C ChevilleLaboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Thai H HoDivision of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ, USA.
Payal KapurDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
James BrugarolasKidney Cancer Program, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
R Houston ThompsonDepartment of Urology, Mayo Clinic, Rochester, MN, USA.
Bradley C LeibovichDepartment of Urology, Mayo Clinic, Rochester, MN, USA.
Eugene D KwonDepartment of Urology, Mayo Clinic, Rochester, MN, USA.
Richard W JosephDivision of Hematology/Oncology, Mayo Clinic, Jacksonville, FL, USA.
Alexander S ParkerDepartment of Health Sciences Research, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 32224, USA. parker.alexander@mayo.edu.
Mayo Clinic in Arizona · USMayo Clinic in Florida · USThe University of Texas Southwestern Medical Center · USMayo Clinic · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
University of Texas Southwestern Medical Center SPORE in Kidney CancerP50CA196516 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI James Brugarolas · 2016 to 2026
$24.7M
Design and Validation of a Biomarker-enhanced System to Predict RCC ProgressionR01CA134466 · NCI · MAYO CLINIC JACKSONVILLE · PI PARKER, ALEXANDER S · 2010 to 2014
$1.7M
Evaluation of the BAP1 tumor suppressor gene in renal cell carcinomaR01CA175754 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI BRUGAROLAS, JAMES · 2014 to 2018
$1.6M
Clinical Impact of B7-H Immune Cell Coregulators in Renal Cell CarcinomaR01CA134345 · NCI · MAYO CLINIC ROCHESTER · PI DONG, HAIDONG, KWON, EUGENE D. · 2009 to 2014
$1.5M
Evaluation of Patient-Matched Primary and Metastatic Samples to Identify and ValiR21CA176422 · NCI · MAYO CLINIC ROCHESTER · PI ECKEL PASSOW, JEANETTE E · 2013 to 2014
$390k
NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA196516NCI NIH HHS R01 CA134345NCI NIH HHS R01 CA134466NCI NIH HHS R01 CA175754NCI NIH HHS R21 CA176422
6 · The paper itself

Abstract

backgroundBAP1 and PBRM1 are frequently mutated in primary clear cell renal cell carcinoma (ccRCC) tumors; however, the frequency and clinical relevance of these mutations in metastatic ccRCC tumors is unknown. Additionally, while intra-tumor heterogeneity has been shown to be common in primary ccRCC, little is known regarding heterogeneity in metastatic ccRCC tumors. MATERIALS AND

methodsWe analyzed BAP1 and PBRM1 loss of protein expression in patient-matched primary and metastatic tumors from 97 patients. Expression was determined using a validated immunohistochemistry assay, which has been shown to be correlated with mutation status.

resultsOf the 97 patients evaluated, 20 and 57% showed loss of BAP1 and PBRM1 in their primary tumors, respectively. Comparing expression across patient-matched primary-metastatic tumor pairs, 98 and 90% had concordant BAP1 and PBRM1 expression, respectively. Both patients who demonstrated discordant BAP1 expression showed loss of BAP1 expression during progression to metastatic ccRCC. Similarly, seven of the ten patients that demonstrated discordant PBRM1 expression showed loss of PBRM1 expression during progression to metastatic ccRCC. We evaluated intra-metastatic tumor heterogeneity using 12 patients who had multiple blocks available from the same tumor with representative pathology; 100 and 92% showed concordant BAP1 and PBRM1 expression, respectively. Amongst 32 patients who had serial metastatic tumors available, both BAP1 and PBRM1 had 97% concordant expression.

conclusionsWe observed minimal intra- and inter- tumor heterogeneity in metastatic ccRCC tumors. Patients with discordant BAP1 or PBRM1 expression across their matched primary and metastatic tumors usually showed loss of expression during progression to metastatic ccRCC.

Indexed as

AdultAgedCarcinoma, Renal CellChromosome DeletionChromosomes, Human, Pair 3DNA-Binding ProteinsFemaleHumansKidney NeoplasmsMaleMiddle AgedMutationNeoplasm MetastasisNuclear ProteinsTranscription FactorsTumor Suppressor ProteinsBAP1 protein, humanDNA-Binding ProteinsNuclear ProteinsPBRM1 protein, humanTranscription FactorsTumor Suppressor ProteinsUbiquitin ThiolesteraseClonalImmunohistochemistryPrognostic

Identifiers

PMID28327121
PMCPMC5361787
OpenAlexW2602237282

What OpenQuestion holds

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Registered trials

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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.