Department of Otorhinolaryngology, Head and Neck Surgery, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Department of Biomedical Research, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Invest New Drugs. 2022 Jun;40(3):478-486. doi: 10.1007/s10637-021-01207-1. Epub 2022 Jan 5.
Resistance to radiation therapy poses a major clinical problem for patients suffering from head and neck squamous cell carcinoma (HNSCC). Transforming growth factor ß (TGF-ß) has emerged as a potential target. This study aimed to investigate the radiosensitizing effect of galunisertib, a small molecule TGF-ß receptor kinase I inhibitor, on HNSCC cells in vitro.
Three HNSCC cell lines were treated with galunisertib alone, or in combination with radiation. Of those three cell lines, one has a known inactivating mutation of the TGF-ß pathway (Cal27), one has a TGF-ß pathway deficiency (FaDu) and one has no known alteration (SCC-25). The effect on metabolic activity was evaluated by a resazurin-based reduction assay. Cell migration was evaluated by wound-healing assay, clonogenic survival by colony formation assay and cell cycle by FACS analysis.
Galunisertib reduced metabolic activity in FaDu, increased in SCC-25 and had no effect on CAL27. Migration was significantly reduced by galunisertib in all three cell lines and showed additive effects in combination with radiation in CAL27 and SCC-25. Colony-forming capabilities were reduced in SCC-25 by galunisertib and also showed an additive effect with adjuvant radiation treatment. Cell cycle analysis showed a reduction of cells in G phase in response to galunisertib treatment.
Our results indicate a potential antineoplastic effect of galunisertib in HNSCC with intact TGF-ß signaling in combination with radiation.
对头颈鳞状细胞癌(HNSCC)患者而言,对放射疗法的抵抗是一个重大的临床问题。转化生长因子β(TGF-β)已成为一个潜在的靶点。本研究旨在研究小分子 TGF-β受体激酶 I 抑制剂 galunisertib 对体外 HNSCC 细胞的放射增敏作用。
用 galunisertib 单独或联合辐射处理三种 HNSCC 细胞系。在这三种细胞系中,有一种已知 TGF-β 途径失活突变(Cal27),有一种 TGF-β 途径缺乏(FaDu),有一种没有已知改变(SCC-25)。通过基于 Resazurin 的还原测定评估对代谢活性的影响。通过划痕愈合测定评估细胞迁移,通过集落形成测定评估克隆存活,通过 FACS 分析评估细胞周期。
Galunisertib 降低了 FaDu 的代谢活性,增加了 SCC-25 的代谢活性,对 CAL27 没有影响。Galunisertib 显著减少了所有三种细胞系的迁移,并且在 CAL27 和 SCC-25 中与放射联合具有相加作用。Galunisertib 降低了 SCC-25 的集落形成能力,并且还与辅助放射治疗表现出相加作用。细胞周期分析显示,细胞在 G 期因 galunisertib 处理而减少。
我们的结果表明,galunisertib 联合放射治疗对具有完整 TGF-β 信号的 HNSCC 具有潜在的抗肿瘤作用。