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SM-1 联合照射对头颈部鳞癌增敏作用的研究。

Study on the sensitizing effect of SM-1 combined with irradiation on head and neck squamous cell carcinoma.

机构信息

Tianjin Key Laboratory of Radiation Medicine and Molecular Nuclear Medicine, Institute of Radiation Medicine, Chinese Academy of Medical Sciences, Tianjin, China.

Department of Life Science and Biological Pharmacy, Shenyang Pharmaceutical University, Shenyang, China.

出版信息

Int J Radiat Biol. 2024;100(10):1453-1461. doi: 10.1080/09553002.2024.2381490. Epub 2024 Aug 13.

Abstract

PURPOSE

Head and neck squamous cell carcinoma (HNSCC) is globally prevalent with high recurrence, low survival rate, and poor quality of life for patients. Derived from PAC-1, SM-1 can activate procaspase-3 and induce apoptosis in cancer cells to exert anti-tumor effects. However, the inhibitory effect of SM-1 on HNSCC after combination with radiation are unclear. This study aims to investigate the radiosensitizing effect of SM-1 on HNSCC in vitro and in vivo.

METHODS

MTT method was used to detect the effect of SM-1 on the viability of HNSCC cell lines (HONE1, HSC-2, and CAL27). The effects of SM-1 combined with radiation on the survival index of HONE1, HSC-2, and CAL27 cell lines were determined by colony formation assay. Flow cytometry was used to investigate the effects of SM-1 and radiation combination on cell apoptosis and cell cycle, and western blot experiments were performed to detect the expression of apoptosis and cell cycle-related proteins. Finally, a xenograft tumor model of CAL27 was established to evaluate the anti-tumor effect of SM-1 combined with radiation in vivo.

RESULTS

In vitro, SM-1 effectively inhibited the activity of HNSCC cell lines HONE1, HSC-2, and CAL27 cells, and synergistically showed anti-proliferation activity during combined irradiation. Meanwhile, anti-tumor effect of SM-1 on HNSCC was higher than that of Debio1143, and the radiosensitivity of cells was greatly increased. Flow cytometry and western blot analysis showed that SM-1 induced G2/M phase arrest of head and neck squamous cell carcinoma cells via inhibiting the expression of CyclinB1 and CDC2. Moreover, SM-1 activated caspase-3 activity and up-regulated the cleaved form of PARP1 to induce cell apoptosis. In vivo, SM-1 combined irradiation showed a good anti-tumor effect.

CONCLUSION

SM-1 enhances HNSCC cell radiation sensitivity in vitro and in vivo, supporting its potential as a radiosensitizer for clinical trials in combination with radiotherapy.

摘要

目的

头颈部鳞状细胞癌(HNSCC)在全球范围内普遍存在,其具有高复发率、低生存率和患者生活质量差的特点。SM-1 源自 PAC-1,可激活前胱天蛋白酶-3,诱导癌细胞凋亡,发挥抗肿瘤作用。然而,SM-1 联合放疗对 HNSCC 的抑制作用尚不清楚。本研究旨在探讨 SM-1 体外和体内对 HNSCC 的放射增敏作用。

方法

采用 MTT 法检测 SM-1 对 HNSCC 细胞系(HONE1、HSC-2 和 CAL27)活力的影响。采用集落形成实验检测 SM-1 联合辐射对 HONE1、HSC-2 和 CAL27 细胞系存活指数的影响。流式细胞术检测 SM-1 和辐射联合作用对细胞凋亡和细胞周期的影响,Western blot 实验检测凋亡和细胞周期相关蛋白的表达。最后,建立 CAL27 移植瘤模型,评价 SM-1 联合辐射的体内抗肿瘤作用。

结果

体外实验中,SM-1 能有效抑制 HNSCC 细胞系 HONE1、HSC-2 和 CAL27 细胞的活性,并在联合照射时表现出协同的抗增殖活性。同时,SM-1 对 HNSCC 的抗肿瘤作用强于 Debio1143,细胞的放射敏感性大大提高。流式细胞术和 Western blot 分析表明,SM-1 通过抑制 CyclinB1 和 CDC2 的表达,诱导头颈部鳞状细胞癌细胞 G2/M 期阻滞。此外,SM-1 激活 caspase-3 活性,上调 cleaved 型 PARP1,诱导细胞凋亡。体内实验中,SM-1 联合照射表现出良好的抗肿瘤效果。

结论

SM-1 增强了 HNSCC 细胞在体外和体内的放射敏感性,支持其作为与放疗联合的临床试验中的放射增敏剂的潜力。

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