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Mitochondrial Complex I Molecular Alterations in Sapajus apella as a Human Gastric Carcinogenesis Model After MNU Exposure.

Journal of medical primatology 2025 Vol.54(2) p. e70017

Dias BDS, Antunes SR, Pinheiro DDR, Burbano RMR, Borges BDN

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[INTRODUCTION] Gastric cancer (GC) remains among the top five global health problems.

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APA Dias BDS, Antunes SR, et al. (2025). Mitochondrial Complex I Molecular Alterations in Sapajus apella as a Human Gastric Carcinogenesis Model After MNU Exposure.. Journal of medical primatology, 54(2), e70017. https://doi.org/10.1111/jmp.70017
MLA Dias BDS, et al.. "Mitochondrial Complex I Molecular Alterations in Sapajus apella as a Human Gastric Carcinogenesis Model After MNU Exposure.." Journal of medical primatology, vol. 54, no. 2, 2025, pp. e70017.
PMID 40166901
DOI 10.1111/jmp.70017

Abstract

[INTRODUCTION] Gastric cancer (GC) remains among the top five global health problems. Therefore, comprehending the tumor energetic behavior is critical to understanding its progression. This study aimed to investigate mitochondrial DNA (mtDNA) alterations in GC cancer cell lines in an animal model.

[MATERIAL AND METHODS] Four mitochondrial genes (COI, ATP8, ND1, and ND3) were analyzed in GC (AGP01, ACP02, ACP03, and PG100) and control (Walker 256 carcinosarcoma) cell lines inoculated in Sapajus apella, exposed and not exposed to N-methyl-N-nitrosourea.

[RESULTS] Two synonymous alterations were identified in ND1. In ND3, a non-synonymous alteration (A10398G ➔ Thr114Ala) may decrease the respiratory chain Complex I efficiency, enhancing cellular reactive oxygen species and contributing to mtDNA damage. As alterations in ND1 and ND3 were observed in highly aggressive cell lines, our results suggest these genes may play crucial roles in energetic efficiency and gastric carcinogenesis.

MeSH Terms

Stomach Neoplasms; Animals; Electron Transport Complex I; Methylnitrosourea; Cell Line, Tumor; DNA, Mitochondrial; Carcinogenesis; Disease Models, Animal; Humans