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April 5, 2026Cancer Research0 citations

Abstract 4716: Disruption of mitochondrial dynamics alters DNA repair capacity in colon cancer

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MCMarion D. CreechUniversity of KentuckyEHErin M. Wolf HorrellTGTianyan GaoUniversity of Kentucky

Key Points

  • The aim is to investigate how mitochondrial dynamics influence DNA repair mechanisms in colon cancer cells.
  • Generated inducible Drp1 knockdown colon cancer cell lines using lentivirus-mediated RNAi.
  • Treated control and Drp1 knockdown cells with radiation or the chemotherapy drug irinotecan to induce DNA damage.
  • Analyzed DNA damage and repair signaling through western blot and RT-qPCR methods.
  • Increased phosphorylation of Drp1 at the S616 site was observed following treatment with irinotecan or radiation.
  • Knockdown of Drp1 led to higher levels of the DNA damage marker γH2AX after treatments, indicating impaired repair.
  • Exogenous fatty acids were shown to reduce γH2AX expression in control cells but had little effect in Drp1 knockdown cells.
  • Fatty acid supplementation improved cell survival following radiation in control cells, but this effect was diminished in Drp1 knockdown cells.

Abstract

Abstract Mitochondrial dynamics refers to a collection of mitochondrial movements, including fission, fusion, and transport. Cancer cells are known to adjust mitochondrial dynamics to provide the metabolic plasticity needed for cell growth, proliferation and migration. We have shown previously that Drp1, a key regulator of mitochondrial fission, plays an important role in mediating fatty acid-induced activation of Wnt/β-catenin signaling in colon cancer. In this study, we determined the functional interaction between mitochondrial dynamics and DNA damage response in colon cancer cells. To disrupt mitochondrial fission, inducible Drp1 knockdown colon cancer cell lines were generated using lentivirus-mediated RNAi. Control and Drp1 knockdown cells were treated with radiation or chemotherapy drug irinotecan to induce DNA damage response. The extent of DNA damage as well as the activation of DNA repair signaling were analyzed by western blot and RT-qPCR. We found that Drp1 was activated upon irinotecan or radiation treatment as shown by increased phosphorylation at S616 site. Interestingly, the expression of γH2AX, a DNA damage marker, induced by irinotecan or radiation treatment was increased in Drp1 knockdown cells, whereas the expression and activation of DNA damage sensing proteins (e.g., ATM and ATR) remained unchanged. To determine if increased fatty acid uptake alters DNA damage, we showed that the presence of exogenous fatty acids attenuated γH2AX expression induced by radiation in control cells whereas knockdown of Drp1 blunted this response. Functionally, the addition of fatty acids increased, while silencing Drp1 decreased, cell survival post radiation as measured by colony formation assays. However, the pro-survival effect of fatty acids was largely abolished in Drp1 knockdown cells. Taken together, our results suggest that fatty acid uptake may enhance DNA repair via a mitochondrial fission-dependent mechanism. This study establishes a functional link between fatty acid metabolism, mitochondrial dynamics, and DNA damage response in colon cancer cells. Citation Format: Marion D. Creech, Erin M. Wolf Horrell, Tianyan Gao. Disruption of mitochondrial dynamics alters DNA repair capacity in colon cancer abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 4716.

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Creech et al. (2026) studied this question.

synapsesocial.com/papers/69d1fca7a79560c99a0a2445https://doi.org/10.1158/1538-7445.am2026-4716
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