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  4. Regional variation in the tumor microenvironment, immune escape and prognostic factors in breast cancer in sub-Saharan Africa
 
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2023
Journal Article
Title

Regional variation in the tumor microenvironment, immune escape and prognostic factors in breast cancer in sub-Saharan Africa

Abstract
The low overall survival rates of patients with breast cancer in sub-Saharan Africa (SSA) are driven by regionally differing tumor biology, advanced tumor stages at diagnosis, and limited access to therapy. However, it is not known whether regional differences in the composition of the tumor microenvironment (TME) exist and affect patients’ prognosis. In this international, multicentre cohort study, 1,237 formalin-fixed, paraffin-embedded breast cancer samples, including samples of the "African Breast Cancer-Disparities in Outcomes (ABC-DO) Study," were analyzed. The immune cell phenotypes, their spatial distribution in the TME, and immune escape mechanisms of breast cancer samples from SSA and Germany (n = 117) were investigated using histomorphology, conventional and multiplex IHC, and RNA expression analysis. The data revealed no regional differences in the number of tumor-infiltrating lymphocytes (TIL) in the 1,237 SSA breast cancer samples, while the distribution of TILs in different breast cancer IHC subtypes showed regional diversity, particularly when compared with German samples. Higher TIL densities were associated with better survival in the SSA cohort (n = 400), but regional differences concerning the predictive value of TILs existed. High numbers of CD163+ macrophages and CD3+CD8+ T cells accompanied by reduced cytotoxicity, altered IL10 and IFNg levels and downregulation of MHC class I components were predominantly detected in breast cancer samples from Western SSA. Features of nonimmunogenic breast cancer phenotypes were associated with reduced patient survival (n = 131). We therefore conclude that regional diversity in the distribution of breast cancer subtypes, TME composition, and immune escape mechanisms should be considered for therapy decisions in SSA and the design of personalized therapies.
Author(s)
Bauer, Marcus
Martin-Luther-Universität Halle-Wittenberg  
Vetter, Martina
Martin-Luther-Universität Halle-Wittenberg
Stückrath, Kathrin
Martin-Luther-Universität Halle-Wittenberg  
Yohannes, Meron
Addis Ababa University
Desalegn, Zelalem
Addis Ababa University
Yalew, Tewodros
Addis Ababa University
Bekuretsion, Yonas
Addis Ababa University
Kenea, Tariku W.
Aira General Hospital
Joffe, Maureen
Wits Health Consortium (PTY) Johannesburg
Berg, Eunice Joy van den
National Health Laboratory Service Johannesburg
Nikulu, Julien Ilunga
l'Unité Pilote du GFAOP, Lubumbashi
Bakarou, Kamate
Service d'Anatomie Bamako
Manraj, Shyam Shunker
Victoria Hospital Candos, Mauritius
Ogunbiyi, Olufemi
University College Hospital Ibadan
Ekanem, Ima Obong A.
University of Calabar Teaching Hospital
Igbinoba, Festus
National Hospital Abuja
Diomandé, Mohenou Isidore Jean Marie
Service d'Anatomie et Cytologie Pathologiques, Abidjan
Adebamowo, Clement Adebayo
University of Maryland School of Medicine, Baltimore
Dzamalala, Charles P.
Malawi College of Medicine, Blantyre
Anele, Angelica A.
Federal Medical Centre Owerri
Zietsman, Annelle
Windhoek Central Hospital
Galukande, Moses
Makerere University Kampala
Foerster, Milena
International Agency for Research on Cancer IARC/WHO Lyon
Dos Santos Silva, Isabel M.
London School of Hygiene and Tropical Medicine LSHTM
Liu, Biying
Africa Cancer Registry Network Oxford
Santos, Pablo Sandro Carvalho
Martin-Luther-Universität Halle-Wittenberg  
Jemal, Ahmedin M.
American Cancer Society, Atlanta
Abebe, Tamrat Befekadu
Addis Ababa University
Wickenhauser, Claudia
Martin-Luther-Universität Halle-Wittenberg  
Seliger, Barbara
Fraunhofer-Institut für Zelltherapie und Immunologie IZI  
McCormack, Valerie Ann
International Agency for Research on Cancer IARC/WHO Lyon
Kantelhardt, Eva Johanna Ohanna
Martin-Luther-Universität Halle-Wittenberg  
Journal
Cancer immunology research  
Open Access
DOI
10.1158/2326-6066.CIR-22-0795
Additional link
Full text
Language
English
Fraunhofer-Institut für Zelltherapie und Immunologie IZI  
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