Huart Camille, Fransolet Maude, Demazy Catherine, Le Calvé Benjamin, Lucas Stéphane, Michiels Carine, Wéra Anne-Catherine
Cellular Biology Research Unit (URBC), Namur Research Institute for Life Sciences (NARILIS), University of Namur (UNamur), 5000 Namur, Belgium.
Laboratory of Analysis by Nuclear Reaction (LARN), Namur Research Institute for Life Sciences (NARILIS), University of Namur (UNamur), 5000 Namur, Belgium.
Cancers (Basel). 2022 Mar 12;14(6):1460. doi: 10.3390/cancers14061460.
Radiotherapy (RT) is a key component of cancer treatment. Although improvements have been made over the years, radioresistance remains a challenge. For this reason, a better understanding of cell fates in response to RT could improve therapeutic options to enhance cell death and reduce adverse effects. Here, we showed that combining RT (photons and protons) to noncytotoxic concentration of PARP inhibitor, Olaparib, induced a cell line-dependent senescence-like phenotype. The senescent cells were characterized by morphological changes, an increase in p21 mRNA expression as well as an increase in senescence-associated β-galactosidase activity. We demonstrated that these senescent cells could be specifically targeted by Navitoclax (ABT-263), a Bcl-2 family inhibitor. This senolytic drug led to significant cell death when combined with RT and Olaparib, while limited cytotoxicity was observed when used alone. These results demonstrate that a combination of RT with PARP inhibition and senolytics could be a promising therapeutic approach for cancer patients.
放射治疗(RT)是癌症治疗的关键组成部分。尽管多年来已取得进展,但放射抗性仍然是一个挑战。因此,更好地了解细胞对放疗的命运可能会改善治疗选择,以增强细胞死亡并减少不良反应。在这里,我们表明,将放疗(光子和质子)与非细胞毒性浓度的PARP抑制剂奥拉帕利联合使用,可诱导细胞系依赖性的衰老样表型。衰老细胞的特征是形态变化、p21 mRNA表达增加以及衰老相关β-半乳糖苷酶活性增加。我们证明,这些衰老细胞可被Bcl-2家族抑制剂Navitoclax(ABT-263)特异性靶向。当与放疗和奥拉帕利联合使用时,这种衰老细胞裂解药物导致显著的细胞死亡,而单独使用时观察到的细胞毒性有限。这些结果表明,放疗与PARP抑制和衰老细胞裂解剂联合使用可能是癌症患者一种有前景的治疗方法。