Evidence map›Paper›PMID 22094876›Full record

ArticleCancer research2012

Integrative genomic analyses of sporadic clear cell renal cell carcinoma define disease subtypes and potential new therapeutic targets.

Vijay R Dondeti, Bradley Wubbenhorst, Priti Lal, John D Gordan, Kurt D'Andrea, Edward F Attiyeh, M Celeste Simon, Katherine L Nathanson

Open access · bronzeAbstract readValidation Study
In one paragraph

Article in Cancer research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

37 citing papers in PubMed, 66 citations in OpenAlex.

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  6. Toward a CRISPR-based mouse model ofProceedings of the National Academy of Sciences of the United States of America · 2024
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  14. Genetic and metabolic hallmarks of clear cell renal cell carcinoma.Biochimica et biophysica acta. Reviews on cancer · 2018
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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

8 authors at 3 institutions in 1 country.

Vijay R DondetiDepartment of Medicine, Abramson Family Cancer Research Institute, Abramson Cancer Center, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Bradley Wubbenhorst
Priti Lal
John D Gordan
Kurt D'Andrea
Edward F Attiyeh
M Celeste Simon
Katherine L Nathanson
Children's Hospital of Philadelphia · USHoward Hughes Medical Institute · USUniversity of Pennsylvania · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
TRANSLATIONAL CONTROL IN ADAPTATION TO HYPOXIAP01CA104838 · NCI · UNIVERSITY OF PENNSYLVANIA · PI DIEHL, JOHN ALAN · 2004 to 2018
$17.6M
Genotype and phenotype predictors in therapy response in renal cell carcinomaR01CA135509 · NCI · UNIVERSITY OF PENNSYLVANIA · PI FLAHERTY, KEITH T, LEE, WILLIAM M · 2009 to 2013
$2.3M
Howard Hughes Medical InstituteNCI NIH HHS 5P30CA016520NCI NIH HHS CA104838NCI NIH HHS CA135509NCI NIH HHS P01 CA104838NCI NIH HHS P30 CA016520NCI NIH HHS R01 CA135509
6 · The paper itself

Abstract

Sporadic clear cell renal cell carcinoma (ccRCC), the most common type of adult kidney cancer, is often associated with genomic copy number aberrations on chromosomes 3p and 5q. Aberrations on chromosome 3p are associated with inactivation of the tumor suppressor gene von-Hippel Lindau (VHL), which activates the hypoxia-inducible factors HIF1α and HIF2α. In contrast, ccRCC genes on chromosome 5q remain to be defined. In this study, we conducted an integrated analysis of high-density copy number and gene expression data for 54 sporadic ccRCC tumors that identified the secreted glycoprotein STC2 (stanniocalcin 2) and the proteoglycan VCAN (versican) as potential 5q oncogenes in ccRCCs. In functional assays, STC2 and VCAN each promoted tumorigenesis by inhibiting cell death. Using the same approach, we also investigated the two VHL-deficient subtypes of ccRCC, which express both HIF1α and HIF2α (H1H2) or only HIF2α (H2). This analysis revealed a distinct pattern of genomic aberrations in each group, with the H1H2 group displaying, on average, a more aberrant genome than the H2 group. Together our findings provide a significant advance in understanding ccRCCs by offering a molecular definition of two subtypes with distinct characteristics as well as two potential chromosome 5q oncogenes, the overexpression of which is sufficient to promote tumorigenesis by limiting cell death.

Indexed as

GenomicsCarcinoma, Renal CellCell Line, TumorGene DosageGene Expression ProfilingHumansKidney Neoplasms

Identifiers

PMID22094876
PMCPMC3251639
OpenAlexW2171126881

What OpenQuestion holds

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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.