Facts and Perspectives: Implications of tumor glycolysis on immunotherapy response in triple negative breast cancer.

immune checkpoint inhibitor (ICI) immune microenviroment regulatory T (Treg) cell triple negative breast cancer (TNBC) tumor glycolysis

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2022
Historique:
received: 05 10 2022
accepted: 17 11 2022
entrez: 27 1 2023
pubmed: 28 1 2023
medline: 28 1 2023
Statut: epublish

Résumé

Triple negative breast cancer (TNBC) is an aggressive disease that is difficult to treat and portends a poor prognosis in many patients. Recent efforts to implement immune checkpoint inhibitors into the treatment landscape of TNBC have led to improved outcomes in a subset of patients both in the early stage and metastatic settings. However, a large portion of patients with TNBC remain resistant to immune checkpoint inhibitors and have limited treatment options beyond cytotoxic chemotherapy. The interplay between the anti-tumor immune response and tumor metabolism contributes to immunotherapy response in the preclinical setting, and likely in the clinical setting as well. Specifically, tumor glycolysis and lactate production influence the tumor immune microenvironment through creation of metabolic competition with infiltrating immune cells, which impacts response to immune checkpoint blockade. In this review, we will focus on how glucose metabolism within TNBC tumors influences the response to immune checkpoint blockade and potential ways of harnessing this information to improve clinical outcomes.

Identifiants

pubmed: 36703796
doi: 10.3389/fonc.2022.1061789
pmc: PMC9872136
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

1061789

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

Copyright © 2023 Schreier, Zappasodi, Serganova, Brown, Demaria and Andreopoulou.

Déclaration de conflit d'intérêts

RZ is an inventor on patent applications related to work on GITR, PD-1, and CTLA-4 (patent numbers: US20180244793A1; US10323091B2; WO2018106864A1; WO2019094352A1). RZ is a scientific advisory board member for iTEOS Belgium SA. SD has received compensation for consultancy/advisory services from Lytix Biopharma, EMD Serono, Ono Pharmaceutical, and Genentech, and research support from Lytix Biopharma and Boehringer-Ingelheim for unrelated projects. AS, IS, KB, and EA do not have any conflicts of interest to declare.

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Auteurs

Ashley Schreier (A)

Division of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medicine, New York Presbyterian Hospital, New York, NY, United States.

Roberta Zappasodi (R)

Division of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY, United States.
Immunology and Microbial Pathogenesis Program, Weill Cornell Graduate School of Medical Sciences, New York, NY, United States.
Parker Institute for Cancer Immunotherapy, San Francisco, CA, United States.

Inna Serganova (I)

Division of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY, United States.
Human Oncology & Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY, United States.

Kristy A Brown (KA)

Department of Medicine, Weill Cornell Medicine, New York, NY, United States.

Sandra Demaria (S)

Department of Radiation Oncology and Department of Pathology, Weill Cornell Medicine, New York, NY, United States.

Eleni Andreopoulou (E)

Division of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medicine, New York Presbyterian Hospital, New York, NY, United States.

Classifications MeSH