Evidence map›Paper›PMID 30718355›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2019

Genetic Ancestry-dependent Differences in Breast Cancer-induced Field Defects in the Tumor-adjacent Normal Breast.

Harikrishna Nakshatri, Brijesh Kumar, Heather N Burney, Mary L Cox, Max Jacobsen, George E Sandusky, Crislyn D'Souza-Schorey, Anna Maria V Storniolo

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.3field-weighted citation impact, top 24% 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

21 citing papers in PubMed, 35 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

8 authors at 3 institutions in 1 country.

Harikrishna NakshatriDepartment of Surgery, Indiana University School of Medicine, Indianapolis, Indiana. hnakshat@iupui.edu.
Brijesh KumarDepartment of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
Heather N BurneyDepartment of Biostatistics, Indiana University School of Medicine, Indianapolis, Indiana.
Mary L CoxDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana.
Max JacobsenDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana.
George E SanduskyDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana.
Crislyn D'Souza-SchoreyDepartment of Biological Sciences, University of Notre Dame, South Bend, Indiana.
Anna Maria V StornioloIU Simon Cancer Center, Indiana University School of Medicine, Indianapolis, Indiana.
Indiana University Health · USIndiana University – Purdue University Indianapolis · USUniversity of Notre Dame · US

Funding

Estrogen-Estrogen Receptor axis in non-transformed breast epithelial cells: studies beyond MCF-7R03CA195250 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI NAKSHATRI, HARIKRISHNA · 2016 to 2017
$156k
NCI NIH HHS R03 CA195250
6 · The paper itself

Abstract

purposeGenetic ancestry influences evolutionary pathways of cancers. However, whether ancestry influences cancer-induced field defects is unknown. The goal of this study was to utilize ancestry-mapped true normal breast tissues as controls to identify cancer-induced field defects in normal tissue adjacent to breast tumors (NATs) in women of African American (AA) and European (EA) ancestry. EXPERIMENTAL

designA tissue microarray comprising breast tissues of ancestry-mapped 100 age-matched healthy women from the Komen Tissue Bank (KTB) at Indiana University (Indianapolis, IN) and tumor-NAT pairs from 100 women (300 samples total) was analyzed for the levels of ZEB1, an oncogenic transcription factor that is central to cell fate, mature luminal cell-enriched estrogen receptor alpha (ERα), GATA3, FOXA1, and for immune cell composition.

resultsZEB1

conclusionsGenetic ancestry-mapped tissues from healthy individuals are required for proper assessment and development of cancer-induced field defects as early cancer detection markers. This finding is significant in light of recent discoveries of influence of genetic ancestry on both normal biology and tumor evolution.

Indexed as

Genetic Predisposition to DiseaseB7-H1 AntigenBiomarkers, TumorBlack or African AmericanBlack PeopleBreastBreast NeoplasmsEstrogen Receptor alphaFemaleGATA3 Transcription FactorHepatocyte Nuclear Factor 3-alphaHumansNeoplastic Stem CellsPrognosisProgrammed Cell Death 1 ReceptorTissue Array AnalysisB7-H1 AntigenBiomarkers, TumorCD274 protein, humanESR1 protein, humanEstrogen Receptor alphaFOXA1 protein, humanGATA3 protein, humanGATA3 Transcription FactorHepatocyte Nuclear Factor 3-alphaPDCD1 protein, humanProgrammed Cell Death 1 ReceptorZEB1 protein, humanZinc Finger E-box-Binding Homeobox 1

Identifiers

PMID30718355
PMCPMC11216537
OpenAlexW2912291459

What OpenQuestion holds

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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.