Accelerated glycolysis in tumor microenvironment is associated with worse survival in triple-negative but not consistently with ER+/HER2- breast cancer.

Breast cancer GSVA glycolysis signaling prognostic biomarker tumor microenvironment

Journal

American journal of cancer research
ISSN: 2156-6976
Titre abrégé: Am J Cancer Res
Pays: United States
ID NLM: 101549944

Informations de publication

Date de publication:
2023
Historique:
received: 07 03 2023
accepted: 06 05 2023
medline: 10 8 2023
pubmed: 10 8 2023
entrez: 10 8 2023
Statut: epublish

Résumé

Metabolic reprogramming to sustain immortality is a hallmark of cancer and glycolysis is an important way to attain this. Thus, we investigate the association of glycolysis and associated pathways in the survival of breast cancer. A total of 5,176 breast cancer patients from multiple independent cohorts were analyzed. We determined the glycolytic signaling score by the degree of enrichment by Gene Set Variant Analysis and the median was used to divide each cohort into high vs low score groups. Glycolysis high breast cancer significantly enriched the hallmark cell proliferation-related gene sets (E2F targets, G2M checkpoint, and MYC targets v1 and v2) and was associated with high

Identifiants

pubmed: 37559984
pmc: PMC10408485

Types de publication

Journal Article

Langues

eng

Pagination

3041-3054

Informations de copyright

AJCR Copyright © 2023.

Déclaration de conflit d'intérêts

None.

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Auteurs

Masanori Oshi (M)

Department of Surgical Oncology, Roswell Park Comprehensive Cancer Center Buffalo, New York 14263, USA.
Department of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine Yokohama 236-0004, Japan.

Arya Mariam Roy (AM)

Department of Medical Oncology, Roswell Park Comprehensive Cancer Center Buffalo, New York 14263, USA.

Li Yan (L)

Department of Biostatistics & Bioinformatics, Roswell Park Comprehensive Cancer Center Buffalo, New York 14263, USA.

Mahato Sasamoto (M)

Department of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine Yokohama 236-0004, Japan.

Yoshihisa Tokumaru (Y)

Department of Surgical Oncology, Roswell Park Comprehensive Cancer Center Buffalo, New York 14263, USA.

Rongrong Wu (R)

Department of Surgical Oncology, Roswell Park Comprehensive Cancer Center Buffalo, New York 14263, USA.

Akimitsu Yamada (A)

Department of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine Yokohama 236-0004, Japan.

Shinya Yamamoto (S)

Department of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine Yokohama 236-0004, Japan.

Takashi Chishima (T)

Department of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine Yokohama 236-0004, Japan.

Kazutaka Narui (K)

Department of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine Yokohama 236-0004, Japan.

Itaru Endo (I)

Department of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine Yokohama 236-0004, Japan.

Kazuaki Takabe (K)

Department of Surgical Oncology, Roswell Park Comprehensive Cancer Center Buffalo, New York 14263, USA.
Department of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine Yokohama 236-0004, Japan.
Department of Surgery, Jacobs School of Medicine and Biomedical Sciences, State University of New York Buffalo, New York 14263, USA.
Division of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences Niigata 951-8520, Japan.
Department of Breast Surgery, Fukushima Medical University School of Medicine Fukushima 960-1295, Japan.
Department of Breast Surgery and Oncology, Tokyo Medical University Tokyo 160-8402, Japan.

Classifications MeSH