Evidence map›Paper›PMID 29912871›Full record

Trial reportPloS one2018

AR negative triple negative or "quadruple negative" breast cancers in African American women have an enriched basal and immune signature.

Melissa Davis, Shweta Tripathi, Raymond Hughley, Qinghua He, Sejong Bae, Balasubramanyam Karanam, Rachel Martini, Lisa Newman, Windy Colomb, William Grizzle and 1 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
2.7field-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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

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  10. The DARC side of genetics in cancer: Breast cancer disparities.American journal of human genetics · 2024
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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

11 authors at 5 institutions in 1 country.

Melissa DavisDepartment of Public Health Sciences, Henry Ford Health Systems and Henry Ford Cancer Institute, Detroit, MI, United States of America.
Shweta TripathiDepartment of Biology & Center for Cancer Research, Tuskegee University, Tuskegee, AL, United States of America.
Raymond HughleyDepartment of Biology & Center for Cancer Research, Tuskegee University, Tuskegee, AL, United States of America.
Qinghua HeDepartment of Chemical Engineering, Auburn University, Auburn, AL, United States of America.
Sejong BaeDivision of Preventive Medicine, University of Alabama at Birmingham School of Medicine, Birmingham, AL, United States of America.
Balasubramanyam KaranamDepartment of Biology & Center for Cancer Research, Tuskegee University, Tuskegee, AL, United States of America.
Rachel MartiniDepartment of Public Health Sciences, Henry Ford Health Systems and Henry Ford Cancer Institute, Detroit, MI, United States of America.
Lisa NewmanDepartment of Surgery, Henry Ford Health Systems and International Center for the Study of Breast Cancer Subtypes, Detroit, MI, United States of America.
Windy ColombDepartment of Oncology, CHRISTUS St. Patrick Hospital, Lake Charles, LA, United States of America.
William GrizzleDepartment of Pathology, University of Alabama at Birmingham School of Medicine, Birmingham, AL, United States of America.
Clayton YatesDepartment of Biology & Center for Cancer Research, Tuskegee University, Tuskegee, AL, United States of America.ORCID 0000-0002-8691-2291
Center for Cancer Research · USHenry Ford Health System · USUniversity of Alabama at Birmingham · USAuburn University · USCHRISTUS St. Patrick Hospital · US

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Tuskegee University Center for Biomedical Research/ Research Centers at Minority InstitutionsU54MD007585 · NIMHD · TUSKEGEE UNIVERSITY · PI Jason Anthony White · 2017 to 2026
$29.4M
TRAINING AND CAREER DEVELOPMENTU54CA118948 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI UPENDER MANNE · 2005 to 2026
$26.6M
Research Training & Career Development ProgramU54CA118638 · NCI · MOREHOUSE SCHOOL OF MEDICINE · PI Desiree Avia Rivers · 2005 to 2026
$22.7M
Research Education CoreU54CA118623 · NCI · TUSKEGEE UNIVERSITY · PI Vivian L Carter, TIMOTHY TURNER · 2005 to 2026
$20.2M
Collaborative Human Tissue NetworkUM1CA183728 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GRIZZLE, WILLIAM E. · 2014 to 2018
$3.7M
Transcriptional Regulation of Breast Cancer Metastasis within the Tumor MicroenviR21CA188799 · NCI · TUSKEGEE UNIVERSITY · PI YATES, CLAYTON · 2014 to 2015
$368k
NCI NIH HHS P30 CA013148NCI NIH HHS R21 CA188799NCI NIH HHS U54 CA118623NCI NIH HHS U54 CA118638NCI NIH HHS U54 CA118948NCI NIH HHS UM1 CA183728NIMHD NIH HHS U54 MD007585
6 · The paper itself

Abstract

There is increasing evidence that Androgen Receptor (AR) expression has prognostic usefulness in Triple negative breast cancer (TNBC), where tumors that lack AR expression are considered "Quadruple negative" Breast Cancers ("QNBC"). However, a comprehensive analysis of AR expression within all breast cancer subtypes or stratified by race has not been reported. We assessed AR mRNA expression in 925 tumors from The Cancer Genome Atlas (TCGA), and 136 tumors in 2 confirmation sets. AR protein expression was determined by immunohistochemistry in 197 tumors from a multi-institutional cohort, for a total of 1258 patients analyzed. Cox hazard ratios were used to determine correlations to PAM50 breast cancer subtypes, and TNBC subtypes. Overall, AR-negative patients are diagnosed at a younger age compared to AR-positive patients, with the average age of AA AR-negative patients being, 49. AA breast tumors express AR at lower rates compared to Whites, independent of ER and PR expression (p<0.0001). AR-negative patients have a (66.60; 95% CI, 32-146) odds ratio of being basal-like compared to other PAM50 subtypes, and this is associated with an increased time to progression and decreased overall survival. AA "QNBC" patients predominately demonstrated BL1, BL2 and IM subtypes, with differential expression of E2F1, NFKBIL2, CCL2, TGFB3, CEBPB, PDK1, IL12RB2, IL2RA, and SOS1 genes compared to white patients. Immune checkpoint inhibitors PD-1, PD-L1, and CTLA-4 were significantly upregulated in both overall "QNBC" and AA "QNBC" patients as well. Thus, AR could be used as a prognostic marker for breast cancer, particularly in AA "QNBC" patients.

Indexed as

Black or African AmericanNeoplasm ProteinsTriple Negative Breast NeoplasmsAdultAlabamaFemaleGene Expression Regulation, NeoplasticHumansMiddle AgedReceptors, AndrogenNeoplasm ProteinsReceptors, Androgen

Identifiers

PMID29912871
PMCPMC6005569
OpenAlexW2809316286

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.