Evidence map›Paper›PMID 37704631›Full record

ArticleNature communications2023

MYC Deregulation and PTEN Loss Model Tumor and Stromal Heterogeneity of Aggressive Triple-Negative Breast Cancer.

Zinab O Doha, Xiaoyan Wang, Nicholas L Calistri, Jennifer Eng, Colin J Daniel, Luke Ternes, Eun Na Kim, Carl Pelz, Michael Munks, Courtney Betts and 19 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

15 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. CircPVT1 weakens miR-33a-5p unleashing the c-MYC/GLS1 metabolic axis in breast cancer.Journal of experimental & clinical cancer research : CR · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Emerging treatment approaches for triple-negative breast cancer.Medical oncology (Northwood, London, England) · 2023
    Review
  15. Article
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

29 authors at 2 institutions in 2 countries.

Zinab O Doha *Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
Xiaoyan Wang *Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
Nicholas L CalistriDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0002-8541-0919
Jennifer EngDepartment of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0003-1499-8417
Colin J DanielDepartment of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
Luke TernesDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.
Eun Na KimDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.
Carl PelzDepartment of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
Michael MunksBrenden-Colson Center for Pancreatic Care, Oregon Health & Science University, Portland, OR, USA.
Courtney BettsDepartment of Cell, Developmental & Cancer Biology, Oregon Health and Science University, Portland, OR, USA.
Sunjong KwonDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.
Elmar BucherDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.
Xi LiDivision of Oncologic Sciences, Oregon Health and Science University, Portland, OR, USA.
Trent WaughDepartment of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
Zuzana TatarovaDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.
Dylan BlumbergDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.
Aaron KoDepartment of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, OR, USA.
Nell KirchbergerDepartment of Cell, Developmental & Cancer Biology, Oregon Health and Science University, Portland, OR, USA.
Jennifer A PietenpolDepartment of Biochemistry, Vanderbilt University Medical Center, Nashville, TN, USA.
Melinda E SandersVanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN, USA.
Ellen M LangerDepartment of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0003-0352-1859
Mu-Shui DaiDepartment of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0001-9031-6962
Gordon MillsBrenden-Colson Center for Pancreatic Care, Oregon Health & Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0002-0144-9614
Koei ChinDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0001-8061-7462
Young Hwan ChangDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0001-8764-1959
Lisa M CoussensBrenden-Colson Center for Pancreatic Care, Oregon Health & Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0003-2389-1865
Joe W GrayDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0001-9225-6756
Laura M HeiserDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0003-3330-0950
Rosalie C SearsDepartment of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, USA. searsr@ohsu.edu.ORCID http://orcid.org/0000-0003-1558-2413
Oregon Health & Science University · USVanderbilt University Medical Center · US

Funding

Understanding the origins of rapid recurrence of pancreatic cancer after resectionP30CA069533 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Luiz Eduardo Bertassoni · 1997 to 2026
$60.5M
TISSUE CoreP50CA098131 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PARK, BEN HO, PIETENPOL, JENNIFER A · 2003 to 2024
$48.7M
Understanding the Impact of Microscale and Nanoscale Heterogeneity and ResistanceU54CA209988 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI GRAY, JOE W. · 2017 to 2021
$10.3M
Hydroxylation regulation of c-MycR01CA186241 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Mu-Shui Dai, ROSALIE C SEARS · 2015 to 2026
$4.2M
Comparative analysis between patient-derived models of pancreatic ductal adenocarcinomas and matched tumor specimensU01CA224012 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI BRODY, JONATHAN, COUSSENS, LISA M. · 2019 to 2023
$2.9M
Regulation of the nucleolar RNA exosome in cancerR01CA262104 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Mu-Shui Dai · 2022 to 2026
$2.3M
Integrated Training in Quantitative and Experimental Cancer Systems BiologyT32CA254888 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Sudarshan Anand, LISA M COUSSENS · 2021 to 2026
$2.2M
c-Myc Phosphorylation Sites Regulate Its Apoptotic and Tumorigenic PotentialR01CA129040 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI SEARS, ROSALIE C · 2008 to 2012
$1.6M
NCI NIH HHS P30 CA069533NCI NIH HHS P50 CA098131NCI NIH HHS R01 CA129040NCI NIH HHS R01 CA186241NCI NIH HHS R01 CA262104NCI NIH HHS T32 CA254888NCI NIH HHS U01 CA224012NCI NIH HHS U54 CA209988
6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) patients have a poor prognosis and few treatment options. Mouse models of TNBC are important for development of new therapies, however, few mouse models represent the complexity of TNBC. Here, we develop a female TNBC murine model by mimicking two common TNBC mutations with high co-occurrence: amplification of the oncogene MYC and deletion of the tumor suppressor PTEN. This Myc;Ptenfl model develops heterogeneous triple-negative mammary tumors that display histological and molecular features commonly found in human TNBC. Our research involves deep molecular and spatial analyses on Myc;Ptenfl tumors including bulk and single-cell RNA-sequencing, and multiplex tissue-imaging. Through comparison with human TNBC, we demonstrate that this genetic mouse model develops mammary tumors with differential survival and therapeutic responses that closely resemble the inter- and intra-tumoral and microenvironmental heterogeneity of human TNBC, providing a pre-clinical tool for assessing the spectrum of patient TNBC biology and drug response.

Indexed as

Mammary Neoplasms, AnimalTriple Negative Breast NeoplasmsAnimalsDisease Models, AnimalFemaleHumansMiceMutationProto-Oncogene Proteins c-mycPTEN PhosphohydrolaseProto-Oncogene Proteins c-mycPTEN PhosphohydrolasePTEN protein, humanPten protein, mouse

Identifiers

PMID37704631
PMCPMC10499828
OpenAlexW4386707566

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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.