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Combinatorial effects of metformin and glucose on the immune evasion of breast cancer 4T1 cells

Duy Khuong Pham 1, 2
Hoai Nam Le 1, 2
Anh Nhu Nguyen 1, 2
Thao Nhi Huynh 1, 3
Chau Nhat Truong 2, 4
Phuc Van Pham 2, 4, 5, * ORCID logo
  1. Laboratory of Stem Cell Research and Application, University of Science, Ho Chi Minh City, Viet Nam
  2. Viet Nam National University Ho Chi Minh City, Ho Chi Minh City, Viet Nam
  3. iet Nam National University Ho Chi Minh City, Ho Chi Minh City, Viet Nam
  4. Stem Cell Institute, University of Science, Ho Chi Minh City, Viet Nam
  5. Laboratory of Cancer Research, University of Science, Ho Chi Minh City, Viet Nam
Correspondence to: Phuc Van Pham, Viet Nam National University Ho Chi Minh City, Ho Chi Minh City, Viet Nam; Stem Cell Institute, University of Science, Ho Chi Minh City, Viet Nam; Laboratory of Cancer Research, University of Science, Ho Chi Minh City, Viet Nam. ORCID: https://orcid.org/0000-0001-7254-0717. Email: phucpham@sci.edu.vn.
Volume & Issue: Vol. 10 No. 10 (2023) | Page No.: 5942-5952 | DOI: 10.15419/bmrat.v10i10.835
Published: 2023-10-30

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This article is published with open access by BioMedPress. This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0) which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. 

Abstract

Introduction: Metformin is one current medicine used to treat type 2 diabetes. Numerous studies have shown that high metformin concentrations have an anti-cancer effect. Therefore, this study aimed to examine whether combining various metformin and glucose concentrations affects mouse breast cancer cell proliferation, migration, and expression of immune escape-related genes.

Methods: This study assessed 12 glucose and metformin combinations: four glucose concentrations (0, 0.5, 1.0, and 4.5 g/L) and three metformin concentrations (0, 2.0, and 5.0 mM). Mouse breast cancer 4T1 cells were cultured in RPMI 1640 media containing these 12 combinations at 37?C with 5% CO2. The combinatorial effects of metformin and glucose were evaluated based on 4T1 cell proliferation, migration, and expression of immune escape-related genes.

Results: Combining 2 mM metformin with 4.5 g/L glucose concentration inhibited 4T1 cell proliferation, migration, and expression of immune escape-related genes.

Conclusion: Our findings provide more information about the anticancer effects of metformin under high glucose conditions, help explain why metformin effectively treats cancer in patients with type 2 diabetes, and suggest combining metformin with glucose in anticancer treatment.

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