Evidence map›Paper›PMID 33623115›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2021

Protein-based immune profiles of basal-like vs. luminal breast cancers.

Andrea Walens, Linnea T Olsson, Xiaohua Gao, Alina M Hamilton, Erin L Kirk, Stephanie M Cohen, Bentley R Midkiff, Yongjuan Xia, Mark E Sherman, Nana Nikolaishvili-Feinberg and 4 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Guideline
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. The Landscape of Immune Microenvironments in Racially Diverse Breast Cancer Patients.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2022
    Article
  11. Review
  12. Effector memory cytotoxic CD3Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Article
  13. Article
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

14 authors at 2 institutions in 2 countries.

Andrea WalensLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, 27599, USA.
Linnea T OlssonDepartment of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC, 27599, USA.
Xiaohua GaoLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, 27599, USA.
Alina M HamiltonDepartment of Pathology and Laboratory Medicine, School of Medicine, University of North Carolina, Chapel Hill, NC, 27599, USA.
Erin L KirkDepartment of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC, 27599, USA.
Stephanie M CohenLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, 27599, USA.
Bentley R MidkiffLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, 27599, USA.ORCID http://orcid.org/0000-0002-6565-9055
Yongjuan XiaLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, 27599, USA.
Mark E ShermanHealth Sciences Research, Mayo Clinic, Jacksonville, FL, 32224, USA.
Nana Nikolaishvili-FeinbergLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, 27599, USA.
Jonathan S SerodyLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, 27599, USA.
Katherine A HoadleyLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, 27599, USA.
Melissa A TroesterLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, 27599, USA. troester@unc.edu.
Benjamin C CalhounLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, 27599, USA. ben.calhoun@unchealth.unc.edu.ORCID http://orcid.org/0000-0001-6505-5430
University of North Carolina at Chapel Hill · USJacksonville College · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
Tissue Procurement & PathologyP50CA058223 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KATHERINE A. HOADLEY · 1992 to 2026
$59.3M
UNC-CH CENTER FOR ENVIRONMENTAL HEALTH &SUSCEPTIBILITYP30ES010126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Melissa A. Troester · 2001 to 2026
$36.3M
Cancer Control Education ProgramT32CA057726 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Melissa B Gilkey, Melissa A. Troester · 2017 to 2026
$3.7M
Impact of the Breast Cancer Immune Microenvironment on Racial Disparities and SurvivorshipF31CA257388 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HAMILTON, ALINA MARIE · 2021 to 2022
$44k
NCI NIH HHS F31 CA257388NCI NIH HHS P30 CA016086NCI NIH HHS P50 CA058223NCI NIH HHS T32 CA057726NIEHS NIH HHS P30 ES010126
6 · The paper itself

Abstract

Tumor-infiltrating lymphocytes play an important, but incompletely understood role in chemotherapy response and prognosis. In breast cancer, there appear to be distinct immune responses by subtype, but most studies have used limited numbers of protein markers or bulk sequencing of RNA to characterize immune response, in which spatial organization cannot be assessed. To identify immune phenotypes of Basal-like vs. Luminal breast cancer we used the GeoMx® (NanoString) platform to perform digital spatial profiling of immune-related proteins in tumor whole sections and tissue microarrays (TMA). Visualization of CD45, CD68, or pan-Cytokeratin by immunofluorescence was used to select regions of interest in formalin-fixed paraffin embedded tissue sections. Forty-four antibodies representing stromal markers and multiple immune cell types were applied to quantify the tumor microenvironment. In whole tumor slides, immune hot spots (CD45+) had increased expression of many immune markers, suggesting a diverse and robust immune response. In epithelium-enriched areas, immune signals were also detectable and varied by subtype, with regulatory T-cell (T

Indexed as

AdultAgedBiomarkers, TumorBreast NeoplasmsFemaleHumansLeukocyte Common AntigensMiddle AgedNeoplasm ProteinsTissue Array AnalysisYoung AdultBiomarkers, TumorLeukocyte Common AntigensNeoplasm ProteinsPTPRC protein, human

Identifiers

PMID33623115
PMCPMC8140991
OpenAlexW3132615309

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.