Effects of High-Linear-Energy-Transfer Heavy Ion Radiation on Intestinal Stem Cells: Implications for Gut Health and Tumorigenesis

Overview

Journal Cancers (Basel)

Publisher MDPI

Specialty Oncology

Date 2024 Oct 16

PMID 39410012

Authors

Santosh Kumar

Shubhankar Suman

Jerry Angdisen

Bo-Hyun Moon

Bhaskar V S Kallakury

Kamal Datta

Albert J Fornace Jr

Affiliations

Soon will be listed here.

Abstract

Heavy ion radiation, prevalent in outer space and relevant for radiotherapy, is densely ionizing and poses a risk to intestinal stem cells (ISCs), which are vital for maintaining intestinal homeostasis. Earlier studies have shown that heavy-ion radiation can cause chronic oxidative stress, persistent DNA damage, cellular senescence, and the development of a senescence-associated secretory phenotype (SASP) in mouse intestinal mucosa. However, the specific impact on different cell types, particularly Lgr5 intestinal stem cells (ISCs), which are crucial for maintaining cellular homeostasis, GI function, and tumor initiation under genomic stress, remains understudied. Using an ISCs-relevant mouse model ( mice) and its GI tumor surrogate ( mice), we investigated ISCs-specific molecular alterations after high-LET radiation exposure. Tissue sections were assessed for senescence and SASP signaling at 2, 5 and 12 months post-exposure. Lgr5+ cells exhibited significantly greater oxidative stress following Si irradiation compared to γ-ray or controls. Both Lgr5 cells and Paneth cells showed signs of senescence and developed a senescence-associated secretory phenotype (SASP) after Si exposure. Moreover, gene expression of pro-inflammatory and pro-growth SASP factors remained persistently elevated for up to a year post-Si irradiation. Additionally, p38 MAPK and NF-κB signaling pathways, which are critical for stress responses and inflammation, were also upregulated after Si radiation. Transcripts involved in nutrient absorption and barrier function were also altered following irradiation. In mice, tumor incidence was significantly higher in those exposed to Si radiation compared to the spontaneous tumorigenesis observed in control mice. Our results indicate that high-LET Si exposure induces persistent DNA damage, oxidative stress, senescence, and SASP in Lgr5 ISCs, potentially predisposing astronauts to altered nutrient absorption, barrier function, and GI carcinogenesis during and after a long-duration outer space mission.

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