Evidence map›Paper›PMID 37190208›Full record

ArticleCancers2023

Immune Profile of Exosomes in African American Breast Cancer Patients Is Mediated by Kaiso/THBS1/CD47 Signaling.

Md Shakir Uddin Ahmed, Brittany D Lord, Benjamin Adu Addai, Sandeep K Singhal, Kevin Gardner, Ahmad Bin Salam, Anghesom Ghebremedhin, Jason White, Iqbal Mahmud, Rachel Martini and 9 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Thrombospondin-1 induces CD8Journal of ovarian research · 2025
    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

19 authors at 12 institutions in 2 countries.

Md Shakir Uddin AhmedDepartment of Biology and Center for Cancer Research, Tuskegee University, Tuskegee, AL 36088, USA.
Brittany D LordDepartment of Genetics, University of Georgia, Athens, GA 30602, USA.
Benjamin Adu AddaiSchool of Veterinary Medicine, Tuskegee University, Tuskegee, AL 36088, USA.
Sandeep K SinghalDepartment of Pathology, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND 58202, USA.ORCID 0000-0002-3486-067X
Kevin GardnerDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, NY 10032, USA.
Ahmad Bin SalamDepartment of Biology and Center for Cancer Research, Tuskegee University, Tuskegee, AL 36088, USA.
Anghesom GhebremedhinDepartment of Biology and Center for Cancer Research, Tuskegee University, Tuskegee, AL 36088, USA.
Jason WhiteDepartment of Biology and Center for Cancer Research, Tuskegee University, Tuskegee, AL 36088, USA.
Iqbal MahmudDepartment of Pathology, Immunology and Laboratory Medicine, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
Rachel MartiniDepartment of Surgery, Weill Cornell Medicine, New York, NY 10065, USA.
Deepa BediDepartment of Biology and Center for Cancer Research, Tuskegee University, Tuskegee, AL 36088, USA.
Huixian LinDepartment of Biology and Center for Cancer Research, Tuskegee University, Tuskegee, AL 36088, USA.
Jacqueline D JonesDepartment of Biological and Environmental Sciences, Troy University, Troy, AL 36082, USA.
Balasubramanyanam KaranamDepartment of Biology and Center for Cancer Research, Tuskegee University, Tuskegee, AL 36088, USA.ORCID 0000-0002-0782-2539
Windy Dean-ColombDepartment of Biology and Center for Cancer Research, Tuskegee University, Tuskegee, AL 36088, USA.
William GrizzleDepartment of Pathology, School of Medicine, The University of Alabama at Birmingham, Birmingham, AL 35233, USA.
Honghe WangDepartment of Biology and Center for Cancer Research, Tuskegee University, Tuskegee, AL 36088, USA.
Melissa DavisDepartment of Surgery, Weill Cornell Medicine, New York, NY 10065, USA.ORCID 0000-0002-6124-6923
Clayton C YatesDepartment of Biology and Center for Cancer Research, Tuskegee University, Tuskegee, AL 36088, USA.ORCID 0000-0001-5420-9852
Center for Cancer Research · USCornell University · USBangladesh Council of Scientific and Industrial Research · BDColumbia University Irving Medical Center · USJohns Hopkins University · USPiedmont Newnan Hospital · USTroy University · USTuskegee University · USUniversity of Alabama at Birmingham · USUniversity of Florida · USUniversity of Georgia · USUniversity of North Dakota · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

African American (AA) women with breast cancer are more likely to have higher inflammation and a stronger overall immune response, which correlate with poorer outcomes. In this report, we applied the nanostring immune panel to identify differences in inflammatory and immune gene expression by race. We observed a higher expression of multiple cytokines in AA patients compared to EA patients, with high expression of CD47, TGFB1, and NFKB1 associated with the transcriptional repressor Kaiso. To investigate the mechanism associated with this expression pattern, we observed that Kaiso depletion results in decreased expression of CD47, and its ligand SIRPA. Furthermore, Kaiso appears to directly bind to the methylated sequences of the THBS1 promotor and repress gene expression. Similarly, Kaiso depletion attenuated tumor formation in athymic nude mice, and these Kaiso-depleted xenograft tissues showed significantly higher phagocytosis and increased infiltration of M1 macrophages. In vitro validation using MCF7 and THP1 macrophages treated with Kaiso-depleted exosomes showed a reduced expression of immune-related markers (CD47 and SIRPA) and macrophage polarization towards the M1 phenotype compared to MCF7 cells treated with exosomes isolated from high-Kaiso cells. Lastly, analysis of TCGA breast cancer patient data demonstrates that this gene signature is most prominent in the basal-like subtype, which is more frequently observed in AA breast cancer patients.

Indexed as

African Americansbreast cancercancer health disparityCD47exosomesimmune signalinginflammationKaisoSIRPATHBS1tumor microenvironment

Identifiers

PMID37190208
PMCPMC10136634
OpenAlexW4365448017

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.