Evidence map›Paper›PMID 30185546›Full record

ArticleCancer research2018

HORMAD1 Is a Negative Prognostic Indicator in Lung Adenocarcinoma and Specifies Resistance to Oxidative and Genotoxic Stress.

Brandt A Nichols, Nathaniel W Oswald, Elizabeth A McMillan, Kathleen McGlynn, Jingsheng Yan, Min S Kim, Janapriya Saha, Prema L Mallipeddi, Sydnie A LaDuke, Pamela A Villalobos and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 66 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

17 authors at 3 institutions in 1 country.

Brandt A NicholsSimmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, Texas.
Nathaniel W OswaldDepartment of Biochemistry, UT Southwestern Medical Center, Dallas, Texas.
Elizabeth A McMillanDepartment of Cell Biology, UT Southwestern Medical Center, Dallas, Texas.
Kathleen McGlynnSimmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, Texas.
Jingsheng YanDepartment of Clinical Sciences, UT Southwestern Medical Center, Dallas, Texas.
Min S KimDepartment of Clinical Sciences, UT Southwestern Medical Center, Dallas, Texas.
Janapriya SahaDepartment of Radiation Oncology, UT Southwestern Medical Center, Dallas, Texas.
Prema L MallipeddiDepartment of Biochemistry, UT Southwestern Medical Center, Dallas, Texas.
Sydnie A LaDukeSimmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, Texas.
Pamela A VillalobosDepartment of Translational Molecular Pathology, M.D. Anderson Cancer Center, Houston, Texas.
Jaime Rodriguez-CanalesDepartment of Translational Molecular Pathology, M.D. Anderson Cancer Center, Houston, Texas.
Ignacio I WistubaDepartment of Translational Molecular Pathology, M.D. Anderson Cancer Center, Houston, Texas.
Bruce A PosnerDepartment of Biochemistry, UT Southwestern Medical Center, Dallas, Texas.
Anthony J DavisDepartment of Radiation Oncology, UT Southwestern Medical Center, Dallas, Texas.
John D MinnaSimmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, Texas.ORCID 0000-0002-7776-0767
John B MacMillanDepartment of Chemistry and Biochemistry, University of California Santa Cruz, Santa Cruz, California.ORCID 0000-0003-1430-1077
Angelique W WhitehurstSimmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, Texas. angelique.whitehurst@utsouthwestern.edu.
Southwestern Medical Center · USThe University of Texas MD Anderson Cancer Center · USUniversity of California, Santa Cruz · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
Transcription-Coupled & Replication-Associated Excision RepairP01CA092584 · NCI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI John A. Tainer · 2001 to 2026
$89.6M
UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GIBBONS, DON LYNN · 1996 to 2024
$57.4M
UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Sandi Leigh Pruitt · 2010 to 2026
$53.7M
Urgent Covid-19 Revision to the Center for High-Throughput Functional Annotation of Natural ProductsU41AT008718 · NCCIH · UT SOUTHWESTERN MEDICAL CENTER · PI CECH, NADJA B, LININGTON, ROGER G · 2015 to 2024
$10.1M
DIVISION OF CELL &MOLECULAR BIOLOGY TRAINING PROGRAMT32GM008203 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI COBB, MELANIE H. · 1987 to 2018
$7.0M
Pathway Choice of DNA Double-Strand Break RepairR01CA162804 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI DAVIS, ANTHONY J · 2012 to 2021
$3.4M
Lung cancer oncogenotype-selective drug target discoveryU01CA176284 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MACMILLAN, JOHN B, MINNA, JOHN D. · 2013 to 2016
$2.8M
Framing Therapeutic Opportunities in Tumor-Activated Gametogenic ProgramsR01CA196905 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI WHITEHURST, ANGELIQUE WRIGHT · 2016 to 2020
$2.0M
Marine Actinomycetes as a Resource for Anticancer Natural ProductsR01CA149833 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MACMILLAN, JOHN B · 2010 to 2014
$1.6M
NCCIH NIH HHS U41 AT008718NCI NIH HHS P01 CA092584NCI NIH HHS P30 CA016086NCI NIH HHS P30 CA016672NCI NIH HHS P30 CA142543NCI NIH HHS P50 CA070907NCI NIH HHS R01 CA149833NCI NIH HHS R01 CA162804NCI NIH HHS R01 CA196905NCI NIH HHS U01 CA176284NIGMS NIH HHS T32 GM008203
6 · The paper itself

Abstract

Cancer testis antigens (CTA) are expressed in testis and placenta and anomalously activated in a variety of tumors. The mechanistic contribution of CTAs to neoplastic phenotypes remains largely unknown. Using a chemigenomics approach, we find that the CTA HORMAD1 correlates with resistance to the mitochondrial complex I inhibitor piericidin A in non-small cell lung cancer (NSCLC). Resistance was due to a reductive intracellular environment that attenuated the accumulation of free radicals. In human lung adenocarcinoma (LUAD) tumors, patients expressing high HORMAD1 exhibited elevated mutational burden and reduced survival. HORMAD1 tumors were enriched for genes essential for homologous recombination (HR), and HORMAD1 promoted RAD51-filament formation, but not DNA resection, during HR. Accordingly, HORMAD1 loss enhanced sensitivity to γ-irradiation and PARP inhibition, and HORMAD1 depletion significantly reduced tumor growth

Indexed as

Gene Expression Regulation, NeoplasticA549 CellsAdenocarcinoma of LungAnimalsAntigens, NeoplasmCarcinoma, Non-Small-Cell LungCell Cycle ProteinsCell Line, TumorCell SurvivalDNA DamageDNA RepairFemaleFree RadicalsGene Expression ProfilingHumansLung NeoplasmsAntigens, NeoplasmCell Cycle ProteinsFree RadicalsHORMAD1 protein, humanMutagens

Identifiers

PMID30185546
PMCPMC6440700
OpenAlexW2891852223

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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.