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

Tong Hu, Gai-Ting Liu, Dan-Dan Wang, Yan-Tao Xiao, Wen-Feng Gou, Dai-Ying Zuo, Wen-Bin Hou, Yi-Liang Li
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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.

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研究 SM-1 联合照射对头颈部鳞状细胞癌的增敏作用。
目的:头颈部鳞状细胞癌(HNSCC)在全球普遍存在,复发率高、生存率低、患者生活质量差。SM-1源自PAC-1,能激活procaspase-3,诱导癌细胞凋亡,从而发挥抗肿瘤作用。然而,SM-1与放射线结合后对HNSCC的抑制作用尚不明确。本研究旨在探讨 SM-1 在体外和体内对 HNSCC 的放射增敏作用:方法:采用 MTT 法检测 SM-1 对 HNSCC 细胞株(HONE1、HSC-2 和 CAL27)活力的影响。通过集落形成试验确定了 SM-1 与辐射结合对 HONE1、HSC-2 和 CAL27 细胞株存活指数的影响。流式细胞术研究了SM-1与辐射联合使用对细胞凋亡和细胞周期的影响,Western印迹实验检测了细胞凋亡和细胞周期相关蛋白的表达。最后,建立了CAL27异种移植肿瘤模型,以评估SM-1与辐射联合在体内的抗肿瘤效果:结果:在体外,SM-1能有效抑制HNSCC细胞株HONE1、HSC-2和CAL27细胞的活性,并在联合辐照时协同显示抗增殖活性。同时,SM-1 对 HNSCC 的抗肿瘤作用高于 Debio1143,细胞的放射敏感性大大提高。流式细胞术和 Western 印迹分析表明,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 期停滞。此外,SM-1 还能激活 Caspase-3 的活性,并上调 PARP1 的裂解形式,从而诱导细胞凋亡。在体内,SM-1联合照射显示出良好的抗肿瘤效果:结论:SM-1能增强HNSCC细胞在体外和体内的辐射敏感性,支持其作为放射增敏剂与放疗联合应用于临床试验的潜力。
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