Mechanism of Musashi2 affecting radiosensitivity of lung cancer by modulating DNA damage repair

Hongjin Qu; Xiong Shi; Ying Xu; Hongran Qin; Junshi Li; Shanlin Cai; Jianpeng Zhao; Bingbing Wan; Yanyong Yang; Bailong Li

doi:10.1002/mco2.548

Mechanism of Musashi2 affecting radiosensitivity of lung cancer by modulating DNA damage repair

MedComm (2020). 2024 Apr 21;5(5):e548. doi: 10.1002/mco2.548. eCollection 2024 May.

Authors

Hongjin Qu^{1

2}, Xiong Shi³, Ying Xu¹, Hongran Qin⁴, Junshi Li¹, Shanlin Cai¹, Jianpeng Zhao¹, Bingbing Wan², Yanyong Yang¹, Bailong Li¹

Affiliations

¹ Department of Radiation Medicine Faculty of Naval Medicine Naval Medical University Shanghai China.
² Key Laboratory of Systems Biomedicine (Ministry of Education) Shanghai Center for Systems Biomedicine Shanghai Jiao Tong University Shanghai China.
³ Shanghai Engineering Research Center of Tooth Restoration and Regeneration Tongji Research Institute of Stomatology Department of Radiology, Stomatological Hospital and Dental School, Tongji University Shanghai China.
⁴ Department of Nuclear Radiation Shanghai Pulmonary Hospital School of Medicine Tongji University Shanghai China.

Abstract

Identifying new targets for overcoming radioresistance is crucial for improving the efficacy of lung cancer radiotherapy, given that tumor cell resistance is a leading cause of treatment failure. Recent research has spotlighted the significance of Musashi2 (MSI2) in cancer biology. In this study, we first demonstrated that MSI2 plays a key function in regulating the radiosensitivity of lung cancer. The expression of MSI2 is negatively correlated with overall survival in cancer patients, and the knockdown of MSI2 inhibits tumorigenesis and increases radiosensitivity of lung cancer cells. Cellular radiosensitivity, which is closely linked to DNA damage, is influenced by MSI2 interaction with ataxia telangiectasia mutated and Rad3-related kinase (ATR) and checkpoint kinase 1 (CHK1) post-irradiation; moreover, knockdown of MSI2 inhibits the ATR-mediated DNA damage response pathway. RNA-binding motif protein 17 (RBM17), which is implicated in DNA damage repair, exhibits increased interaction with MSI2 post-irradiation. We found that knockdown of RBM17 disrupted the interaction between MSI2 and ATR post-irradiation and increased the radiosensitivity of lung cancer cells. Furthermore, we revealed the potential mechanism of MSI2 recruitment into the nucleus with the assistance of RBM17 to activate ATR to promote radioresistance. This study provides novel insights into the potential application of MSI2 as a new target in lung cancer radiotherapy.

Keywords: DNA damage repair; Musashi2 (MSI2); RNA‐binding motif protein 17 (RBM17); ataxia telangiectasia mutated and Rad3‐related kinase (ATR); lung cancer; radioresistance; radiosensitivity.