Evidence map›Paper›PMID 33113091›Full record

ArticleBreast cancer research and treatment2021

Inflammation markers on benign breast biopsy are associated with risk of invasive breast cancer in African American women.

Asra N Shaik, Katrin Kiavash, Karri Stark, Julie L Boerner, Julie J Ruterbusch, Hany Deirawan, Sudeshna Bandyopadhyay, Rouba Ali-Fehmi, Gregory Dyson, Michele L Cote

Abstract read
In one paragraph

Article in Breast cancer research and treatment, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 8 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

10 authors at 3 institutions in 1 country.

Asra N ShaikDepartment of Oncology, Wayne State University School of Medicine, Detroit, MI, USA.
Katrin KiavashDepartment of Pathology, Anatomy and Laboratory Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.
Karri StarkBarbara Ann Karmanos Cancer Institute, 4100 John R. St, Mailstop: MM04EP, Detroit, MI, 48201, USA.
Julie L BoernerDepartment of Oncology, Wayne State University School of Medicine, Detroit, MI, USA.
Julie J RuterbuschDepartment of Oncology, Wayne State University School of Medicine, Detroit, MI, USA.
Hany DeirawanDepartment of Pathology, Wayne State University School of Medicine, Detroit, MI, USA.
Sudeshna BandyopadhyayDepartment of Pathology, Wayne State University School of Medicine, Detroit, MI, USA.
Rouba Ali-FehmiDepartment of Pathology, Wayne State University School of Medicine, Detroit, MI, USA.
Gregory DysonDepartment of Oncology, Wayne State University School of Medicine, Detroit, MI, USA.
Michele L CoteDepartment of Oncology, Wayne State University School of Medicine, Detroit, MI, USA. cotem@karmanos.org.ORCID http://orcid.org/0000-0003-0312-1601
Wayne State University · USThe Barbara Ann Karmanos Cancer Institute · USWest Virginia University · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI PAUL M STEMMER · 1985 to 2026
$68.4M
NCI NIH HHS 1F31CA22133301NCI NIH HHS P30 CA022453Susan G. Komen for the Cure GTDR14299348Susan G. Komen for the Cure IIRG #222547
6 · The paper itself

Abstract

purposeMarkers of inflammation, including crown-like structures of the breast (CLS-B) and infiltrating lymphocytes (IL), have been identified in breast tissue and associated with increased risk of breast cancer (BrCa), however most of this work has been performed in primarily non-Hispanic white women. Here, we examined whether CLS-B and IL are associated with invasive BrCa in African American (AA) women.

methodsWe assessed breast biopsies from three 5-year age-matched groups: BrCa-free AA women (50 Volunteer) from the Komen Normal Tissue Bank (KTB) and AA women with a clinically-indicated biopsy diagnosed with benign breast disease (BBD) from our Detroit cohort who developed BrCa (55 BBD-cancer) or did not develop BrCa (47 BBD only, year of biopsy matched to BBD-cancer). Mean adipocyte diameter and total adipose area were estimated from digital images using the Adiposoft plugin from ImageJ. Associations between CLS-B, IL, and BrCa among KTB and Detroit biopsies were assessed using multivariable multinomial and conditional logistic regression models.

resultsAmong all biopsies, Volunteer and BBD only biopsies did not harbor CLS-B or IL at significantly different rates after adjusting for logarithm of adipocyte area, adipocyte diameter, and BMI. Among clinically-indicated BBD biopsies, BBD-cancer biopsies were more likely to exhibit CLS-B (odds ratio (OR) = 3.36, 95% Confidence Interval (CI): 1.33-8.48) or IL (OR = 4.95, 95% CI 1.76-13.9) than BBD only biopsies after adjusting for total adipocyte area, adipocyte diameter, proliferative disease, and BMI.

conclusionsCLS-B and IL may serve as histological markers of BrCa risk in benign breast biopsies from AA women.

Indexed as

Breast NeoplasmsBiopsyBlack or African AmericanBreastFemaleHumansInflammationRisk FactorsAfrican americanBenign breast diseaseBreast cancer riskInflammationObesity

Identifiers

PMID33113091
PMCPMC12311869
OpenAlexW3096534692

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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.