Abstract

The cell cycle checkpoint system play a pivotal role in the cellular DNA damage response, and the discovery of checkpoint inhibitors is expected to sensitize current cancer therapies. Checkpoint signaling cascades are critically modulated by ATM (ataxia telangiectasia-mutated) and its related molecules. Generally, ATM primarily responds to ionizing irradiation-induced DNA double-strand breaks. Heavy ions from an accelerated carbon ion beam have been used to cure cancer because they are more effective than ionizing irradiation such as X-ray and γ-radiation in terms of biological damage. In a previous study, we demonstrated that a persimmon leaf flavonol (PLF) promoted the cytotoxic effect of chemotherapeutic agents on cancer cells through inhibition of checkpoint activities, especially in the ATM dependent pathway. The present study investigated whether PLF inhibits checkpoint activity during the DNA damage response induced by heavy ion irradiation. Treatment with PLF significantly increased the cytotoxicity of heavy ion irradiation in A549 adenocarcinoma cells. The phosphorylation of checkpoint proteins such as p53, SMC1, and Chk1 was increased by heavy ions. PLF reduced the phosphorylation of checkpoint proteins. Pre-treatment with PLF significantly prevented the decrease of mitotic cells in heavy ion-exposed cells. We further evaluated tumor volume in SCID mice inoculated with human lung adenocarcinoma A549 cells. The combination treatment of PLF and heavy ion resulted in a decrease of tumor volume compared with controls, although PLF itself did not exhibit any effect. These results indicate that PLF inhibits tumor growth through modulation of the DNA damage response. PLF may be useful for clinical application in combination with heavy ion radiotherapy.

Highlights

  • Heavy ion radiotherapy has recently received increasing attention in the field of radiotherapy because heavy ion irradiation is more effective than other types of ionizing irradiation such as X-ray or γ-radiation in inducing biological damage [1]

  • We investigated whether persimmon leaf flavonol (PLF) inhibits checkpoint activity during the DNA damage response induced by heavy ion irradiation

  • We reported that PLF promoted the cytotoxic effect of chemotherapeutic agents doxorubicin (DOX) on cancer cells by inhibiting checkpoint activity [10]

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Summary

Introduction

Heavy ion radiotherapy has recently received increasing attention in the field of radiotherapy because heavy ion irradiation is more effective than other types of ionizing irradiation such as X-ray or γ-radiation in inducing biological damage [1]. The carbon ion beam used in heavy ion irradiation releases a large amount of energy at the end of its range and enables the safe delivery of an effective dose of irradiation to cancer tissues without damaging normal tissues [2]. At the DNA damage checkpoint, ATM (ataxia telangiectasia mutated) and ATR (AT and Rad related) play a central role in intracellular signal transduction and control the cell cycle precisely, by phosphorylating downstream components of the checkpoint pathway [5,6,7]. When DNA damage occurs, checkpoint effector proteins such as p53, structural maintenance of chromosomes 1 (SMC1), and checkpoint kinase 1 (Chk1) are phosphorylated and activated by ATM or ATR, which leads to cell cycle arrest in the G1, S, G2, and M phase, respectively. The DNA damage checkpoint induces cell cycle arrest and/or apoptosis.

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