Abstract
In spite of the novel strategies to treat colon cancer, mortality rates associated with this disease remain consistently high. Tumour recurrence has been linked to the induction of resistance towards chemotherapy that involves cellular events that enable cancer cells to escape cell death. Treatment of colon cancer mainly implicates direct or indirect DNA-damaging agents and increased repair or tolerances towards subsequent lesions contribute to generate resistant populations. Resveratrol (RSV), a potent chemosensitising polyphenol, might share common properties with chemotherapeutic drugs through its indirect DNA-damaging effects reported in vitro. In this study, we investigated how RSV exerts its anticancer effects in models of colon cancer with a particular emphasis on the DNA-damage response (DDR; PIKKs-Chks-p53 signalling cascade) and its cellular consequences. We showed in vitro and in vivo that colon cancer models could progressively escape the repeated pharmacological treatments with RSV. We observed for the first time that this response was correlated with transient activation of the DDR, of apoptosis and senescence. In vitro, a single treatment with RSV induced a DDR correlated with S-phase delay and apoptosis, but prolonged treatments led to transient micronucleations and senescence phenotypes associated with polyploidisation. Ultimately, stable resistant populations towards RSV displaying higher degrees of ploidy and macronucleation as compared to parental cells emerged. We linked these transient effects and resistance emergence to the abilities of these cells to progressively escape RSV-induced DNA damage. Finally, we demonstrated that this DNA damage was triggered by an overproduction of reactive oxygen species (ROS) against which cancer cells could adapt under prolonged exposure to RSV. This study provides a pre-clinical analysis of the long-term effects of RSV and highlights ROS as main agents in RSV's indirect DNA-damaging properties and consequences in terms of anticancer response and potent resistance emergence.
Highlights
The DNA-damage response (DDR) is initiated by the phosphatidylinositol 3-kinaserelated kinases (PIKKs) Ataxia Telangiectasia Mutated (ATM), ATM and Rad3-related (ATR) and DNA-PKcs that elicit
We demonstrated that RSV-induced DNA damage was triggered by an overproduction of reactive oxygen species (ROS) against which cancer cells could adapt under prolonged exposure to RSV
We studied the effects of RSV towards CCR models in vivo and in vitro
Summary
The DDR is initiated by the phosphatidylinositol 3-kinaserelated kinases (PIKKs) ATM, ATR and DNA-PKcs that elicit. Phase I/II clinical trials have shown that administration of RSV was correlated with a 5% reduction of tumour growth in patients with confirmed CCR, despite its low Abbreviations: ATM, Ataxia Telangiectasia Mutated; ATR, ATM and Rad3-related; CCR, Colorectal Cancer; Chk[1], Checkpoint kinase 1; Chk[2], Checkpoint kinase 2; DDR, DNA Damage Response; DNA-PKcs, DNA-dependent Protein Kinase, catalytic subunit; PIKKs, Phosphatidylinositol 3-kinase-related kinases; ROS, Reactive Oxygen Species; RSV, Resveratrol; SA-β-galactosidase, Senescence-Associated β-galactosidase; TRAIL, Tumour-necrosis-factor Related Apoptosis Inducing ligand; TUNEL, TdT-mediated dUTP Nick-End Labelling. We demonstrated that RSV-induced DNA damage was triggered by an overproduction of reactive oxygen species (ROS) against which cancer cells could adapt under prolonged exposure to RSV These effects have to be considered pre-clinically to further point out RSV as a potent chemosensitising agent
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