Evidence map›Paper›PMID 32929263›Full record

ArticleNature biotechnology2021

Oncoprotein-specific molecular interaction maps (SigMaps) for cancer network analyses.

Joshua Broyde, David R Simpson, Diana Murray, Evan O Paull, Brennan W Chu, Somnath Tagore, Sunny J Jones, Aaron T Griffin, Federico M Giorgi, Alexander Lachmann and 4 more

Open access · greenAbstract read
In one paragraph

Article in Nature biotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 37 citations in OpenAlex.

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  11. The application of patient-derived organoid in the research of lung cancer.Cellular oncology (Dordrecht, Netherlands) · 2023
    Review
  12. Article
  13. Frontiers in systems biology · 2023
    Article
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  15. Article
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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

14 authors at 5 institutions in 2 countries.

Joshua Broyde *Department of Systems Biology, Columbia University Irving Medical Center, New York, NY, USA.
David R Simpson *Division of Pediatric Hematology/Oncology, Department of Pediatrics, UCSF Benioff Children's Hospital, San Francisco, CA, USA.
Diana Murray *Department of Systems Biology, Columbia University Irving Medical Center, New York, NY, USA.ORCID http://orcid.org/0000-0003-4121-1536
Evan O PaullDepartment of Systems Biology, Columbia University Irving Medical Center, New York, NY, USA.
Brennan W ChuDepartment of Systems Biology, Columbia University Irving Medical Center, New York, NY, USA.
Somnath TagoreDepartment of Systems Biology, Columbia University Irving Medical Center, New York, NY, USA.
Sunny J JonesDepartment of Systems Biology, Columbia University Irving Medical Center, New York, NY, USA.
Aaron T GriffinDepartment of Systems Biology, Columbia University Irving Medical Center, New York, NY, USA.
Federico M GiorgiCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-7325-9908
Alexander LachmannMount Sinai Center for Bioinformatics; Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Peter JacksonBaxter Laboratory, Department of Microbiology & Immunology, Stanford University, Palo Alto, CA, USA.
E Alejandro Sweet-CorderoDivision of Pediatric Hematology/Oncology, Department of Pediatrics, UCSF Benioff Children's Hospital, San Francisco, CA, USA. alejandro.sweet-cordero@ucsf.edu.ORCID http://orcid.org/0000-0002-9787-9351
Barry HonigDepartment of Systems Biology, Columbia University Irving Medical Center, New York, NY, USA. bh6@cumc.columbia.edu.
Andrea CalifanoDepartment of Systems Biology, Columbia University Irving Medical Center, New York, NY, USA. ac2248@cumc.columbia.edu.ORCID http://orcid.org/0000-0003-4742-3679
Columbia University Irving Medical Center · USUCSF Benioff Children's Hospital · USMount Sinai Medical Center · USPalo Alto University · USUniversity of Cambridge · GB

Funding

Leveraging innovative technologies in basic and clinical cancer researchT32CA009302 · NCI · STANFORD UNIVERSITY · PI LAURA D ATTARDI, Aaron M Newman · 1985 to 2026
$19.1M
Predicting Cancer Cell Response to Endogenous and Exogenous Perturbations at the Single Cell LevelR35CA197745 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ANDREA CALIFANO · 2015 to 2026
$11.5M
Systematic pharmacological targeting of the core mechanisms responsible for maintaining cancer cell stateU54CA209997 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA, HONIG, BARRY H · 2016 to 2021
$10.9M
TRAINING IN CELLULAR, MOLECULAR AND BIOPHYSICAL STUDIEST32GM008224 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI LIEM, RONALD K. · 1987 to 2021
$9.9M
Systems Biology of Tumor Progression and Drug ResistanceU01CA168426 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2012 to 2016
$6.5M
COMPUTER STUDIES OF PROTEIN STRUCTURE AND FUNCTIONR01GM030518 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI HONIG, BARRY H · 1985 to 2020
$4.5M
High-performance compute cluster for biomedical computingS10OD012351 · OD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2012 to 2012
$2.0M
Novel effectors of Kras in oncogenesis, senescence and tumor progressionR01CA129562 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SWEET-CORDERO, ERIC ALEJANDRO · 2009 to 2016
$1.9M
Training Program in Computational BiologyT32GM082797 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HONIG, BARRY H · 2008 to 2015
$1.4M
Storage System for High Performance ComputingS10OD021764 · OD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2016 to 2016
$600k
NCI NIH HHS R01 CA129562NCI NIH HHS R35 CA197745NCI NIH HHS T32 CA009302NCI NIH HHS U01 CA168426NCI NIH HHS U54 CA209997NIGMS NIH HHS R01 GM030518NIGMS NIH HHS T32 GM008224NIGMS NIH HHS T32 GM082797NIH HHS S10 OD012351NIH HHS S10 OD021764
6 · The paper itself

Abstract

Tumor-specific elucidation of physical and functional oncoprotein interactions could improve tumorigenic mechanism characterization and therapeutic response prediction. Current interaction models and pathways, however, lack context specificity and are not oncoprotein specific. We introduce SigMaps as context-specific networks, comprising modulators, effectors and cognate binding-partners of a specific oncoprotein. SigMaps are reconstructed de novo by integrating diverse evidence sources-including protein structure, gene expression and mutational profiles-via the OncoSig machine learning framework. We first generated a KRAS-specific SigMap for lung adenocarcinoma, which recapitulated published KRAS biology, identified novel synthetic lethal proteins that were experimentally validated in three-dimensional spheroid models and established uncharacterized crosstalk with RAB/RHO. To show that OncoSig is generalizable, we first inferred SigMaps for the ten most mutated human oncoproteins and then for the full repertoire of 715 proteins in the COSMIC Cancer Gene Census. Taken together, these SigMaps show that the cell's regulatory and signaling architecture is highly tissue specific.

Indexed as

Gene Regulatory NetworksAlgorithmsAnimalsHumansMiceMutationNeoplasmsOncogene ProteinsOrganoidsProto-Oncogene Proteins p21(ras)RNA, Small InterferingROC CurveSignal TransductionKRAS protein, humanOncogene ProteinsProto-Oncogene Proteins p21(ras)RNA, Small Interfering

Identifiers

PMID32929263
PMCPMC7878435
OpenAlexW3085677572

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.