Evidence map›Paper›PMID 36207580›Full record

ArticleCommunications biology2022

A multi-omic analysis of MCF10A cells provides a resource for integrative assessment of ligand-mediated molecular and phenotypic responses.

Sean M Gross, Mark A Dane, Rebecca L Smith, Kaylyn L Devlin, Ian C McLean, Daniel S Derrick, Caitlin E Mills, Kartik Subramanian, Alexandra B London, Denis Torre and 40 more

Abstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. QSAR Modeling for Predicting ICInternational journal of molecular sciences · 2025
    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

50 authors.

Sean M GrossDepartment of Biomedical Engineering, OHSU, Portland, OR, USA.
Mark A DaneDepartment of Biomedical Engineering, OHSU, Portland, OR, USA.ORCID 0000-0003-3742-9866
Rebecca L SmithDepartment of Biomedical Engineering, OHSU, Portland, OR, USA.
Kaylyn L DevlinDepartment of Biomedical Engineering, OHSU, Portland, OR, USA.
Ian C McLeanDepartment of Biomedical Engineering, OHSU, Portland, OR, USA.ORCID 0000-0003-2741-7941
Daniel S DerrickDepartment of Biomedical Engineering, OHSU, Portland, OR, USA.
Caitlin E MillsLaboratory of Systems Pharmacology, Department of Systems Biology, Harvard Program in Therapeutic Science, Harvard Medical School, Boston, MA, USA.ORCID 0000-0002-2608-4084
Kartik SubramanianLaboratory of Systems Pharmacology, Department of Systems Biology, Harvard Program in Therapeutic Science, Harvard Medical School, Boston, MA, USA.
Alexandra B LondonDepartment of Pharmacological Sciences, Mount Sinai Center for Bioinformatics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Denis TorreDepartment of Pharmacological Sciences, Mount Sinai Center for Bioinformatics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
John Erol EvangelistaDepartment of Pharmacological Sciences, Mount Sinai Center for Bioinformatics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Daniel J B ClarkeDepartment of Pharmacological Sciences, Mount Sinai Center for Bioinformatics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Zhuorui XieDepartment of Pharmacological Sciences, Mount Sinai Center for Bioinformatics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Cemal ErdemDepartment of Chemical and Biomolecular Engineering, Clemson University, Clemson, SC, USA.ORCID 0000-0003-3663-3646
Nicholas LyonsBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Ted NatoliBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Sarah PessaBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Xiaodong LuBroad Institute of MIT and Harvard, Cambridge, MA, USA.
James MullahooBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Jonathan LiDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Miriam AdamDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Brook WassieDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Moqing LiuDepartment of Biomedical Engineering, OHSU, Portland, OR, USA.
David F KilburnDepartment of Biomedical Engineering, OHSU, Portland, OR, USA.
Tiera A LibyDepartment of Biomedical Engineering, OHSU, Portland, OR, USA.
Elmar BucherDepartment of Biomedical Engineering, OHSU, Portland, OR, USA.ORCID 0000-0002-2929-2460
Crystal Sanchez-AguilaDepartment of Biomedical Engineering, OHSU, Portland, OR, USA.
Kenneth DailySage Bionetworks, Seattle, WA, USA.
Larsson OmbergSage Bionetworks, Seattle, WA, USA.
Yunguan WangLaboratory of Systems Pharmacology, Department of Systems Biology, Harvard Program in Therapeutic Science, Harvard Medical School, Boston, MA, USA.
Connor JacobsonLaboratory of Systems Pharmacology, Department of Systems Biology, Harvard Program in Therapeutic Science, Harvard Medical School, Boston, MA, USA.
Clarence YappLaboratory of Systems Pharmacology, Department of Systems Biology, Harvard Program in Therapeutic Science, Harvard Medical School, Boston, MA, USA.
Mirra ChungLaboratory of Systems Pharmacology, Department of Systems Biology, Harvard Program in Therapeutic Science, Harvard Medical School, Boston, MA, USA.
Dusica VidovicSylvester Comprehensive Cancer Center, University of Miami, Miami, FL, 33136, USA.
Yiling LuDepartment of Genomic Medicine, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Stephan SchurerSylvester Comprehensive Cancer Center, University of Miami, Miami, FL, 33136, USA.ORCID 0000-0001-7180-0978
Albert LeeHeart, Lung, and Blood Institute, National Institutes of Health, Bethesda, USA.
Ajay PillaiHuman Genome Research Institute, National Institutes of Health, Bethesda, USA.
Aravind SubramanianBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Malvina PapanastasiouBroad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0003-3378-6612
Ernest FraenkelBroad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0001-9249-8181
Heidi S FeilerDepartment of Biomedical Engineering, OHSU, Portland, OR, USA.ORCID 0000-0002-6580-3547
Gordon B MillsKnight Cancer Institute, OHSU, Portland, OR, USA.
Jake D JaffeBroad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0001-9845-1210
Avi Ma'ayanDepartment of Pharmacological Sciences, Mount Sinai Center for Bioinformatics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Marc R BirtwistleDepartment of Chemical and Biomolecular Engineering, Clemson University, Clemson, SC, USA.
Peter K SorgerLaboratory of Systems Pharmacology, Department of Systems Biology, Harvard Program in Therapeutic Science, Harvard Medical School, Boston, MA, USA.ORCID 0000-0002-3364-1838
James E KorkolaDepartment of Biomedical Engineering, OHSU, Portland, OR, USA.
Joe W GrayDepartment of Biomedical Engineering, OHSU, Portland, OR, USA.
Laura M HeiserDepartment of Biomedical Engineering, OHSU, Portland, OR, USA. heiserl@ohsu.edu.ORCID 0000-0003-3330-0950

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Understanding the origins of rapid recurrence of pancreatic cancer after resectionP30CA069533 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Grace B Gill · 1997 to 2026
$60.5M
Data Coordination and Integration Center for LINCS-BD2KU54HL127624 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MA'AYAN, AVI, SCHURER, STEPHAN C · 2014 to 2019
$23.5M
Discovering existing medicines that abrogate cellular responses to SARS CoV-2 infectionU54HL127366 · NHLBI · BROAD INSTITUTE, INC. · PI GOLUB, TODD R. · 2014 to 2020
$14.3M
Pharmaco Response Signatures and Disease MechanismU54HL127365 · NHLBI · HARVARD MEDICAL SCHOOL · PI SORGER, PETER KARL · 2014 to 2019
$13.1M
Drug Combination Signatures for Prediction and Mitigation of ToxicityU54HG008098 · NHGRI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BIRTWISTLE, MARC R., BIRTWISTLE, MARC R. · 2014 to 2019
$11.8M
Neuron and Glial Cellular Signatures from Normal and Diseased iPS Cells-SupplementU54NS091046 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI FINKBEINER, STEVEN M, FRAENKEL, ERNEST · 2014 to 2020
$11.7M
OutreachU54HG008100 · NHGRI · OREGON HEALTH & SCIENCE UNIVERSITY · PI GRAY, JOE W., HEISER, LAURA MADELINE · 2014 to 2019
$10.5M
There and Back Again: Epigenetic Reinforcement of Cellular Signaling States - OverallU54HG008097 · NHGRI · BROAD INSTITUTE, INC. · PI JAFFE, JACOB DAVID · 2014 to 2019
$9.3M
Graduate Training in Computational and Systems BiologyT32GM087237 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BURGE, CHRISTOPHER B · 2009 to 2023
$4.6M
Predicting the Heterogeneity of Cell-Fate DecisionsR01GM104184 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BIRTWISTLE, MARC R. · 2014 to 2018
$1.8M
NCI NIH HHS P30 CA016672NCI NIH HHS P30 CA069533NHGRI NIH HHS U54 HG008097NHGRI NIH HHS U54 HG008098NHGRI NIH HHS U54 HG008100NHLBI NIH HHS U54 HL127365NHLBI NIH HHS U54 HL127366NHLBI NIH HHS U54 HL127624NIGMS NIH HHS R01 GM104184NIGMS NIH HHS T32 GM087237NINDS NIH HHS U54 NS091046U.S. Department of Health & Human Services | National Institutes of Health (NIH) U54-HG008097U.S. Department of Health & Human Services | National Institutes of Health (NIH) U54-HG008100U.S. Department of Health & Human Services | National Institutes of Health (NIH) U54HL127366U.S. Department of Health & Human Services | National Institutes of Health (NIH) U54HL127624U.S. Department of Health & Human Services | National Institutes of Health (NIH) U54NS091046
6 · The paper itself

Abstract

The phenotype of a cell and its underlying molecular state is strongly influenced by extracellular signals, including growth factors, hormones, and extracellular matrix proteins. While these signals are normally tightly controlled, their dysregulation leads to phenotypic and molecular states associated with diverse diseases. To develop a detailed understanding of the linkage between molecular and phenotypic changes, we generated a comprehensive dataset that catalogs the transcriptional, proteomic, epigenomic and phenotypic responses of MCF10A mammary epithelial cells after exposure to the ligands EGF, HGF, OSM, IFNG, TGFB and BMP2. Systematic assessment of the molecular and cellular phenotypes induced by these ligands comprise the LINCS Microenvironment (ME) perturbation dataset, which has been curated and made publicly available for community-wide analysis and development of novel computational methods ( synapse.org/LINCS_MCF10A ). In illustrative analyses, we demonstrate how this dataset can be used to discover functionally related molecular features linked to specific cellular phenotypes. Beyond these analyses, this dataset will serve as a resource for the broader scientific community to mine for biological insights, to compare signals carried across distinct molecular modalities, and to develop new computational methods for integrative data analysis.

Indexed as

Epidermal Growth FactorProteomicsExtracellular Matrix ProteinsLigandsPhenotypeEpidermal Growth FactorExtracellular Matrix ProteinsLigands

Identifiers

PMID36207580
PMCPMC9546880

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.