Evidence map›Paper›PMID 33527138›Full record

ArticleHuman molecular genetics2021

Sexual dimorphism in cancer: insights from transcriptional signatures in kidney tissue and renal cell carcinoma.

Ruhina S Laskar, Peng Li, Szilvia Ecsedi, Behnoush Abedi-Ardekani, Geoffroy Durand, Nivonirina Robinot, Jean-Noël Hubert, Vladimir Janout, David Zaridze, Anush Mukeria and 15 more

Open access · hybridAbstract read
In one paragraph

Article in Human molecular genetics, 2021. 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
8.8field-weighted citation impact, top 1% 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, 41 citations in OpenAlex.

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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

25 authors at 10 institutions in 8 countries.

Ruhina S LaskarSection of Genetics, International Agency for Research on Cancer (IARC-WHO), 69372 Lyon, France.
Peng LiLaboratory of Population Health, Max Planck Institute for Demographic Research, 18057 Rostock, Germany.
Szilvia EcsediSection of Genetics, International Agency for Research on Cancer (IARC-WHO), 69372 Lyon, France.
Behnoush Abedi-ArdekaniSection of Genetics, International Agency for Research on Cancer (IARC-WHO), 69372 Lyon, France.
Geoffroy DurandSection of Genetics, International Agency for Research on Cancer (IARC-WHO), 69372 Lyon, France.
Nivonirina RobinotSection of Genetics, International Agency for Research on Cancer (IARC-WHO), 69372 Lyon, France.
Jean-Noël HubertSection of Genetics, International Agency for Research on Cancer (IARC-WHO), 69372 Lyon, France.
Vladimir JanoutScience and Research Center, Faculty of Health Sciences, Palacky University, 77900 Olomouc, Czech Republic.
David ZaridzeDepartment of Epidemiology and Prevention, Russian N.N. Blokhin Cancer Research Centre, 115478 Moscow, Russian Federation.
Anush MukeriaDepartment of Epidemiology and Prevention, Russian N.N. Blokhin Cancer Research Centre, 115478 Moscow, Russian Federation.
Dana MatesDepartment of Environmental Health, National Institute of Public Health, 050463 Bucharest, Romania.
Ivana HolcatovaDepartment of Public Health and Preventive Medicine, Charles University, Second Faculty of Medicine, 15006 Prague, Czech Republic.
Lenka ForetovaDepartment of Cancer Epidemiology and Genetics, Masaryk Memorial Cancer Institute, 60200 Brno, Czech Republic.
Beata SwiatkowskaDepartment of Environmental Epidemiology, Nofer Institute of Occupational Medicine, 91-348 Lodz, Poland.
Zoran DzamicClinic of Urology, Clinical Center of Serbia (KCS), University of Belgrade - Faculty of Medicine, 11000 Belgrade, Serbia.
Sasa MilosavljevicInternational Organisation for Cancer Prevention and Research, 11070 Belgrade, Serbia.
Robert OlasoUniversité Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, 91057, Evry, France.
Anne BolandUniversité Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, 91057, Evry, France.
Jean-François DeleuzeUniversité Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, 91057, Evry, France.
David C MullerFaculty of Medicine, School of Public Health, Imperial College London, W21NY London, UK.
James D McKaySection of Genetics, International Agency for Research on Cancer (IARC-WHO), 69372 Lyon, France.
Paul BrennanSection of Genetics, International Agency for Research on Cancer (IARC-WHO), 69372 Lyon, France.
Florence Le Calvez-KelmSection of Genetics, International Agency for Research on Cancer (IARC-WHO), 69372 Lyon, France.
Ghislaine SceloSection of Genetics, International Agency for Research on Cancer (IARC-WHO), 69372 Lyon, France.
Estelle ChanudetSection of Genetics, International Agency for Research on Cancer (IARC-WHO), 69372 Lyon, France.ORCID 0000-0003-0936-9253
Centre international de recherche sur le cancer · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRRussian Cancer Research Center NN Blokhin · RUCharles University · CZImperial College London · GBMasaryk Memorial Cancer Institute · CZMax Planck Institute for Demographic Research · DENofer Institute of Occupational Medicine · PLPalacký University Olomouc · CZUniversity of Belgrade · RS

Funding

Pooled genome-wide analysis of kidney cancer riskU01CA155309 · NCI · INTERNATIONAL AGENCY FOR RES ON CANCER · PI SCELO, GHISLAINE · 2011 to 2014
$3.7M
Cancer Research UK 24390NCI NIH HHS U01 CA155309World Health Organization 001
6 · The paper itself

Abstract

Sexual dimorphism in cancer incidence and outcome is widespread. Understanding the underlying mechanisms is fundamental to improve cancer prevention and clinical management. Sex disparities are particularly striking in kidney cancer: across diverse populations, men consistently show unexplained 2-fold increased incidence and worse prognosis. We have characterized genome-wide expression and regulatory networks of 609 renal tumors and 256 non-tumor renal tissues. Normal kidney displayed sex-specific transcriptional signatures, including higher expression of X-linked tumor suppressor genes in women. Sex-dependent genotype-phenotype associations unraveled women-specific immune regulation. Sex differences were markedly expanded in tumors, with male-biased expression of key genes implicated in metabolism, non-malignant diseases with male predominance and carcinogenesis, including markers of tumor infiltrating leukocytes. Analysis of sex-dependent RCC progression and survival uncovered prognostic markers involved in immune response and oxygen homeostasis. In summary, human kidney tissues display remarkable sexual dimorphism at the molecular level. Sex-specific transcriptional signatures further shape renal cancer, with relevance for clinical management.

Indexed as

Gene Expression ProfilingGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseSex CharacteristicsAgedBiomarkers, TumorCarcinoma, Renal CellDisease ProgressionFemaleGenes, Tumor SuppressorGenes, X-LinkedGenetic Association StudiesGenome-Wide Association StudyHumansKidney NeoplasmsMaleBiomarkers, Tumor

Identifiers

PMID33527138
PMCPMC8098110
OpenAlexW3127148490

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.