Evidence map›Paper›PMID 32376773›Full record

ArticleCancer discovery2020

Somatic Tissue Engineering in Mouse Models Reveals an Actionable Role for WNT Pathway Alterations in Prostate Cancer Metastasis.

Josef Leibold, Marcus Ruscetti, Zhen Cao, Yu-Jui Ho, Timour Baslan, Min Zou, Wassim Abida, Judith Feucht, Teng Han, Francisco M Barriga and 15 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer discovery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

40 citing papers in PubMed, 58 citations in OpenAlex.

  1. Trial
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  6. Article
  7. ATAD2 Drives Prostate Cancer Progression to Metastasis.Molecular cancer research : MCR · 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

25 authors at 4 institutions in 1 country.

Josef Leibold *Department of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.
Marcus Ruscetti *Department of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID https://orcid.org/0000-0002-4394-2087
Zhen Cao *Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York.
Yu-Jui HoDepartment of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.
Timour BaslanDepartment of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.
Min ZouDepartments of Pharmacology, Urology, Medicine, Pathology and Cell Biology, and Systems Biology, Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, New York.
Wassim AbidaDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Judith FeuchtCenter for Cell Engineering and Immunology Program, Memorial Sloan Kettering Cancer Center, New York, New York.
Teng HanWeill Cornell Graduate School of Medical Sciences, Weill Cornell Medicine, New York, New York.
Francisco M BarrigaDepartment of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.
Kaloyan M TsanovDepartment of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID https://orcid.org/0000-0001-9007-4844
Leah ZamechekDepartment of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID https://orcid.org/0000-0003-2863-2950
Amanda KulickDepartment of Molecular Pharmacology, Memorial Sloan Kettering Cancer Center, New York, New York.
Corina AmorDepartment of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.
Sha TianDepartment of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.
Katarzyna RybczykDepartment of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.
Nelson R SalgadoDepartment of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID https://orcid.org/0000-0003-2056-341X
Francisco J Sánchez-RiveraDepartment of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID https://orcid.org/0000-0002-8466-8563
Philip A WatsonHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York.
Elisa de StanchinaDepartment of Molecular Pharmacology, Memorial Sloan Kettering Cancer Center, New York, New York.
John E WilkinsonDepartment of Pathology, University of Michigan, Ann Arbor, Michigan.
Lukas E DowSandra and Edward Meyer Cancer Center, Department of Medicine, Weill Cornell Medicine, New York, New York.ORCID https://orcid.org/0000-0001-7048-1418
Cory Abate-ShenDepartments of Pharmacology, Urology, Medicine, Pathology and Cell Biology, and Systems Biology, Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, New York.
Charles L SawyersHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York. lowes@mskcc.org sawyersc@mskcc.org.ORCID https://orcid.org/0000-0003-4955-6475
Scott W LoweDepartment of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York. lowes@mskcc.org sawyersc@mskcc.org.ORCID https://orcid.org/0000-0002-5284-9650
Memorial Sloan Kettering Cancer Center · USColumbia University Irving Medical Center · USCornell University · USUniversity of Michigan · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
SPORE In Prostate CancerP50CA092629 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI JAMES A EASTHAM · 2001 to 2026
$63.0M
Scientific ReagentsP01CA087497 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI PRIVES, CAROL, STOCKWELL, BRENT R. · 2000 to 2021
$35.4M
MSKCC Pilot Center for Precision Disease ModelingU54OD020355 · OD · SLOAN-KETTERING INST CAN RESEARCH · PI LOWE, SCOTT W., SOLIT, DAVID B. · 2015 to 2019
$9.9M
The MSKCC-UW/Fred Hutch Prostate Cancer Drug Resistance and Sensitivity CenterU54CA224079 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SAWYERS, CHARLES L. · 2017 to 2021
$6.8M
Preclinical analyses of advanced prostate cancer in genetically-engineered miceR01CA173481 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Cory Abate-Shen · 2013 to 2026
$6.1M
Role of ETS factors in specifying prostate luminal cell identity and androgen receptor dependenceR01CA193837 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SAWYERS, CHARLES L. · 2015 to 2025
$4.7M
Molecular mechanisms of prostate cancer metastasisR01CA183929 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ABATE-SHEN, CORY · 2015 to 2025
$4.1M
Understanding Resistance to Next Generation AntiandrogensR01CA155169 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SAWYERS, CHARLES L. · 2012 to 2022
$3.8M
Rapid and flexible precision oncology mouse models of epithelial malignancies epithelial malignanciesR01CA233944 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI LOWE, SCOTT W. · 2020 to 2024
$2.4M
Translational Research in Oncology Training ProgramT32CA160001 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SAWYERS, CHARLES L. · 2011 to 2020
$2.0M
Senescence-Associated Secretory Phenotype (SASP) modulation of the tumor microenvironment as a therapeutic strategy for KRAS-driven tumorsK99CA241110 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI RUSCETTI, MARCUS A. · 2019 to 2019
$137k
Howard Hughes Medical InstituteNCI NIH HHS K99 CA241110NCI NIH HHS P01 CA087497NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA092629NCI NIH HHS R01 CA155169NCI NIH HHS R01 CA173481NCI NIH HHS R01 CA183929NCI NIH HHS R01 CA193837NCI NIH HHS R01 CA233944NCI NIH HHS T32 CA160001NCI NIH HHS U54 CA224079NIH HHS U54 OD020355
6 · The paper itself

Abstract

To study genetic factors influencing the progression and therapeutic responses of advanced prostate cancer, we developed a fast and flexible system that introduces genetic alterations relevant to human disease directly into the prostate glands of mice using tissue electroporation. These electroporation-based genetically engineered mouse models (EPO-GEMM) recapitulate features of traditional germline models and, by modeling genetic factors linked to late-stage human disease, can produce tumors that are metastatic and castration-resistant. A subset of tumors with

Indexed as

AnimalsDisease Models, AnimalHumansMaleMiceNeoplasm MetastasisProstatic NeoplasmsTissue EngineeringWnt Signaling Pathway

Identifiers

PMID32376773
PMCPMC7334089
OpenAlexW3021572418

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.