Evidence map›Paper›PMID 33576900›Full record

ArticleBreast cancer research and treatment2021

Multiethnic PDX models predict a possible immune signature associated with TNBC of African ancestry.

Evelyn M Jiagge, Peter J Ulintz, Shukmei Wong, Sean P McDermott, Sabrina I Fossi, Tahra K Suhan, Mark J Hoenerhoff, Jessica M Bensenhaver, Barbara Salem, Michele Dziubinski and 17 more

Abstract read
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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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The Power and Promise of Patient-Derived Xenografts of Human Breast Cancer.Cold Spring Harbor perspectives in medicine · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Article
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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

27 authors at 7 institutions in 2 countries.

Evelyn M JiaggeHenry Ford Cancer Institute/Henry Ford Health System, 2799 W Grand Blvd, Detroit, MI, 48202, USA. ejiagge1@hfhs.org.ORCID http://orcid.org/0000-0002-5708-0326
Peter J UlintzDepartment of Internal Medicine, Michigan Medicine, University of Michigan, 1500 East Medical Center Drive, RCC 7314, Ann Arbor, MI, 48105, USA.
Shukmei WongThe Translational Genomics Research Institute, Phoenix, AZ, USA.
Sean P McDermottDepartment of Internal Medicine, Michigan Medicine, University of Michigan, 1500 East Medical Center Drive, RCC 7314, Ann Arbor, MI, 48105, USA.
Sabrina I FossiHenry Ford Cancer Institute/Henry Ford Health System, 2799 W Grand Blvd, Detroit, MI, 48202, USA.
Tahra K SuhanRogel Cancer Center, University of Michigan, Ann Arbor, MI, 48105, USA.
Mark J HoenerhoffUnit for Laboratory Animal Medicine, University of Michigan, Ann Arbor, USA.
Jessica M BensenhaverHenry Ford Cancer Institute/Henry Ford Health System, 2799 W Grand Blvd, Detroit, MI, 48202, USA.
Barbara SalemMichigan Institute for Clinical & Health Research, Ann Arbor, USA.
Michele DziubinskiRogel Cancer Center, University of Michigan, Ann Arbor, MI, 48105, USA.
Joseph K OppongKomfo Anokye Teaching Hospital, Kumasi, Ghana.
Francis AitpillahKomfo Anokye Teaching Hospital, Kumasi, Ghana.
Kyei IshmaelKomfo Anokye Teaching Hospital, Kumasi, Ghana.
Ernest Osei-BonsuKomfo Anokye Teaching Hospital, Kumasi, Ghana.
Ernest AdjeiKomfo Anokye Teaching Hospital, Kumasi, Ghana.
Awuah BaffourKomfo Anokye Teaching Hospital, Kumasi, Ghana.
Jessica AldrichThe Translational Genomics Research Institute, Phoenix, AZ, USA.
Ahmet KurdogluThe Translational Genomics Research Institute, Phoenix, AZ, USA.
Kurt FernandoHenry Ford Cancer Institute/Henry Ford Health System, 2799 W Grand Blvd, Detroit, MI, 48202, USA.
David W CraigKeck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Jeff M TrentThe Translational Genomics Research Institute, Phoenix, AZ, USA.
Jun LiRogel Cancer Center, University of Michigan, Ann Arbor, MI, 48105, USA.
Dhananjay ChitaleHenry Ford Cancer Institute/Henry Ford Health System, 2799 W Grand Blvd, Detroit, MI, 48202, USA.
Lisa A NewmanNew York-Presbyterian/Weill Cornell Medical Center and Weill Cornell Medicine, New York, NY, USA.
John D CarptenKeck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Max S WichaDepartment of Internal Medicine, Michigan Medicine, University of Michigan, 1500 East Medical Center Drive, RCC 7314, Ann Arbor, MI, 48105, USA.
Sofia D MerajverDepartment of Internal Medicine, Michigan Medicine, University of Michigan, 1500 East Medical Center Drive, RCC 7314, Ann Arbor, MI, 48105, USA. smerajve@med.umich.edu.
University of Michigan · USKomfo Anokye Teaching Hospital · GHHenry Ford Health System · USTranslational Genomics Research Institute · USUniversity of Southern California · USCornell University · USMichigan Medicine · US

Funding

Breast Cancer Research Foundation No grant numberHorace H. Rackham School of Graduate Studies, University of Michigan No grant numberMETAvivor No grant numberSusan G. Komen for the Cure No grant numberUniversity of Michigan Comprehensive Cancer Center P30 CA 046592
6 · The paper itself

Abstract

purposeTriple-negative breast cancer (TNBC) is an aggressive subtype most prevalent among women of Western Sub-Saharan African ancestry. It accounts for 15-25% of African American (AA) breast cancers (BC) and up to 80% of Ghanaian breast cancers, thus contributing to outcome disparities in BC for black women. The aggressive biology of TNBC has been shown to be regulated partially by breast cancer stem cells (BCSC) which mediate tumor recurrence and metastasis and are more abundant in African breast tumors.

methodsWe studied the biological differences between TNBC in women with African ancestry and those of Caucasian women by comparing the gene expression of the BCSC. From low-passage patient derived xenografts (PDX) from Ghanaian (GH), AA, and Caucasian American (CA) TNBCs, we sorted for and sequenced the stem cell populations and analyzed for differential gene enrichment.

resultsIn our cohort of TNBC tumors, we observed that the ALDH expressing stem cells display distinct ethnic specific gene expression patterns, with the largest difference existing between the GH and AA ALDH+ cells. Furthermore, the tumors from the women of African ancestry [GH/AA] had ALDH stem cell (SC) enrichment for expression of immune related genes and processes. Among the significantly upregulated genes were CD274 (PD-L1), CXCR9, CXCR10 and IFI27, which could serve as potential drug targets.

conclusionsFurther exploration of the role of immune regulated genes and biological processes in BCSC may offer insight into developing novel approaches to treating TNBC to help ameliorate survival disparities in women with African ancestry.

Indexed as

Triple Negative Breast NeoplasmsBlack or African AmericanFemaleGhanaHumansNeoplasm Recurrence, LocalWhite PeopleAfrican ancestryBreast cancer stem cellsGene expressionTriple-negative breast cancer

Identifiers

PMID33576900
OpenAlexW3126689185

What OpenQuestion holds

Textmetadata
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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.