Evidence map›Paper›PMID 27275014›Full record

ArticleJCI insight2016

Deficiency of mitochondrial modulator MCJ promotes chemoresistance in breast cancer.

Maria J Fernández-Cabezudo, Issam Faour, Kenneth Jones, Devin P Champagne, Mohammed A Jaloudi, Yassir A Mohamed, Ghada Bashir, Saeeda Almarzooqi, Alia Albawardi, M Jawad Hashim and 9 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 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

19 authors at 2 institutions in 2 countries.

Maria J Fernández-CabezudoDepartment of Biochemistry, College of Medicine & Health Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.
Issam FaourDepartment of Surgery, Tawam Hospital-Johns Hopkins Medicine, Al-Ain, United Arab Emirates.
Kenneth JonesDepartment of Biochemistry and Molecular Genetics, University of Colorado School of Medicine, Aurora, Colorado, USA.
Devin P ChampagneDepartment of Medicine/Immunobiology Division, University of Vermont, Burlington, Vermont, USA.
Mohammed A JaloudiDepartment of Medical Oncology, Tawam Hospital-Johns Hopkins Medicine, Al-Ain, United Arab Emirates.
Yassir A MohamedDepartment of Medical Microbiology & Immunology, United Arab Emirates University, Al-Ain, United Arab Emirates.
Ghada BashirDepartment of Medical Microbiology & Immunology, United Arab Emirates University, Al-Ain, United Arab Emirates.
Saeeda AlmarzooqiDepartment of Pathology, United Arab Emirates University, Al-Ain, United Arab Emirates.
Alia AlbawardiDepartment of Pathology, United Arab Emirates University, Al-Ain, United Arab Emirates.
M Jawad HashimFamily Medicine, College of Medicine & Health Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.
Thomas S RobertsDepartment of Medicine/Immunobiology Division, University of Vermont, Burlington, Vermont, USA.
Haytham El-SalhatDepartment of Surgery, Tawam Hospital-Johns Hopkins Medicine, Al-Ain, United Arab Emirates.
Hakam El-TajiDepartment of Surgery, Tawam Hospital-Johns Hopkins Medicine, Al-Ain, United Arab Emirates.
Adnan KassisDepartment of Clinical Imaging, Tawam Hospital-Johns Hopkins Medicine, Al-Ain, United Arab Emirates.
Dylan E O'SullivanDepartments of Epidemiology, Pharmacology and Toxicology, and Community and Family Medicine, Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire, USA.
Brock C ChristensenDepartments of Epidemiology, Pharmacology and Toxicology, and Community and Family Medicine, Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire, USA.
James DeGregoriDepartment of Biochemistry and Molecular Genetics, University of Colorado School of Medicine, Aurora, Colorado, USA.
Basel K Al-RamadiDepartment of Medical Microbiology & Immunology, United Arab Emirates University, Al-Ain, United Arab Emirates.
Mercedes RinconDepartment of Medicine/Immunobiology Division, University of Vermont, Burlington, Vermont, USA.
United Arab Emirates University · AEUniversity of Colorado Denver · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Relation Between In-utero Vitamin D and Immune Function in Early Childhood P20GM104416 · NIGMS · DARTMOUTH COLLEGE · PI CHRISTENSEN, BROCK CLARKE · 2013 to 2022
$23.7M
MicroRNA related genetic variation and head and neck cancerR01DE022772 · NIDCR · DARTMOUTH COLLEGE · PI CHRISTENSEN, BROCK CLARKE · 2013 to 2016
$2.7M
Vermont Immunology/Infectious Diseases Training GrantT32AI055402 · NIAID · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI GARY E WARD · 2005 to 2026
$2.7M
MCJ function in mouse mammary tumor propertiesR21CA127099 · NCI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI RINCON, MERCEDES · 2008 to 2009
$438k
Regulation of mitochondrial function in T cellsR21AI110016 · NIAID · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI RINCON, MERCEDES · 2014 to 2015
$419k
NCI NIH HHS P30 CA046934NCI NIH HHS R21 CA127099NIAID NIH HHS R21 AI110016NIAID NIH HHS T32 AI055402NIDCR NIH HHS R01 DE022772NIGMS NIH HHS P20 GM104416
6 · The paper itself

Abstract

Despite major advances in early detection and prognosis, chemotherapy resistance is a major hurdle in the battle against breast cancer. Identifying predictive markers and understanding the mechanisms are key steps to overcoming chemoresistance. Methylation-controlled J protein (MCJ, also known as DNAJC15) is a negative regulator of mitochondrial respiration and has been associated with chemotherapeutic drug sensitivity in cancer cell lines. Here we show, in a retrospective study of a large cohort of breast cancer patients, that low MCJ expression in breast tumors predicts high risk of relapse in patients treated with chemotherapy; however, MCJ expression does not correlate with response to endocrine therapy. In a prospective study in breast cancer patients undergoing neoadjuvant therapy, low MCJ expression also correlates with poor clinical response to chemotherapy and decreased disease-free survival. Using MCJ-deficient mice, we demonstrate that lack of MCJ is sufficient to induce mammary tumor chemoresistance in vivo. Thus, loss of expression of this endogenous mitochondrial modulator in breast cancer promotes the development of chemoresistance.

Identifiers

PMID27275014
PMCPMC4888911
OpenAlexW2401350638

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.