Abstract 2554: Caloric restriction ameliorates aging and tumor progression via tumor immunity in syngeneic mice model

Abstract Background: Caloric restriction (CR) without malnutrition reportedly improves life span and ameliorates aging in preclinical models. Decreased expressions of aging-related genes and inflammation-related genes have been observed in CR mice. Moreover, CR decreases cancer risk and inhibits tumor progression, but the underlying mechanisms are not fully understood. Methods: In this study, we developed a syngeneic model using C57BL/6N male mice, and verified the tumor-suppressing mechanisms of CR. Mice were randomized into 2 groups: normal diet (ND) group fed with ad lib diet, and CR group with 30% reduced feeding compared with the ND group, started from 2 months age. MC38, murine colorectal adenocarcinoma cells, were implanted subcutaneously. We compared tumor growth and survival between the CR group and the ND group. Moreover, to verify the contribution of tumor immunity, we compared the tumor-suppressing effects of anti-PD-1 antibody between the CR group and the ND group. To clarify the impacts of CD8+ cytotoxic T cells, we also conducted CD8 depletion by anti-CD8 antibody. Results: Firstly, we observed significantly restricted tumor progression of the CR group in aged mice, but it was relatively modest in young mice. Secondly, the tumor-suppressing effect of anti-PD-1 was equivalent between the CR group and the ND group in aged mice, which suggests tumor immunity is essential to demonstrate anti-tumor effects in CR mice. However, CD8 depletion in CR mice showed only partial tumor-promoting effects, which suggests immune function excluding CD8+ T cells contributes to suppressing tumor progression in the CR group. Conclusion: Our findings suggest that CR ameliorates aging and tumor progression. Promoted immune function, especially immune cells excluding CD8+ T cells, might play a role in the tumor-suppressing effects of CR. CD4 depletion and comprehensive analyses of intratumoral T cells are currently underway to elucidate the underlying mechanisms of tumor suppression induced by CR. Citation Format: Taichi Horino, Haruki Horiguchi, Yuji Miyamoto, Masaaki Iwatsuki, Yuichi Oike. Caloric restriction ameliorates aging and tumor progression via tumor immunity in syngeneic mice model [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 2554.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2025-04-21
DOI
https://doi.org/10.1158/1538-7445.am2025-2554
Primary Topic
Tryptophan and brain disorders
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 2554: Caloric restriction ameliorates aging and tumor progression via tumor immunity in syngeneic mice model

Yuichi Oike, Yuji Miyamoto, Haruki Horiguchi, Taichi Horino et al.
1 links
Cancer Research
Tryptophan and brain disorders
article

Abstract 2554: Caloric restriction ameliorates aging and tumor progression via tumor immunity in syngeneic mice model

Yuichi Oike, Yuji Miyamoto, Haruki Horiguchi, Taichi Horino, Masaaki Iwatsuki
article en

Abstract

Abstract Background: Caloric restriction (CR) without malnutrition reportedly improves life span and ameliorates aging in preclinical models. Decreased expressions of aging-related genes and inflammation-related genes have been observed in CR mice. Moreover, CR decreases cancer risk and inhibits tumor progression, but the underlying mechanisms are not fully understood. Methods: In this study, we developed a syngeneic model using C57BL/6N male mice, and verified the tumor-suppressing mechanisms of CR. Mice were randomized into 2 groups: normal diet (ND) group fed with ad lib diet, and CR group with 30% reduced feeding compared with the ND group, started from 2 months age. MC38, murine colorectal adenocarcinoma cells, were implanted subcutaneously. We compared tumor growth and survival between the CR group and the ND group. Moreover, to verify the contribution of tumor immunity, we compared the tumor-suppressing effects of anti-PD-1 antibody between the CR group and the ND group. To clarify the impacts of CD8+ cytotoxic T cells, we also conducted CD8 depletion by anti-CD8 antibody. Results: Firstly, we observed significantly restricted tumor progression of the CR group in aged mice, but it was relatively modest in young mice. Secondly, the tumor-suppressing effect of anti-PD-1 was equivalent between the CR group and the ND group in aged mice, which suggests tumor immunity is essential to demonstrate anti-tumor effects in CR mice. However, CD8 depletion in CR mice showed only partial tumor-promoting effects, which suggests immune function excluding CD8+ T cells contributes to suppressing tumor progression in the CR group. Conclusion: Our findings suggest that CR ameliorates aging and tumor progression. Promoted immune function, especially immune cells excluding CD8+ T cells, might play a role in the tumor-suppressing effects of CR. CD4 depletion and comprehensive analyses of intratumoral T cells are currently underway to elucidate the underlying mechanisms of tumor suppression induced by CR. Citation Format: Taichi Horino, Haruki Horiguchi, Yuji Miyamoto, Masaaki Iwatsuki, Yuichi Oike. Caloric restriction ameliorates aging and tumor progression via tumor immunity in syngeneic mice model [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 2554.

Cancer ResearchVol. 85(8_Supplement_1)
Kumamoto City Hospital (JP), Kumamoto University (JP)
Openalex Percentile: Top 92%
Tryptophan and brain disorders
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.