Faculté de Médecine-Lyon-Sud, Université Lyon 1, 69921, Oullins, France.
Laboratoire de Radiobiologie Cellulaire et Moléculaire, Faculté de Médecine Lyon Sud, CNRS UMR 5822 IP2I, 165 Chemin du Grand Revoyet, BP 12, 69921, Oullins Cedex, France.
J Cancer Res Clin Oncol. 2021 Jul;147(7):1905-1916. doi: 10.1007/s00432-021-03593-8. Epub 2021 Mar 31.
The clinical outcome of head and neck squamous cell carcinoma (HNSCC) remains poor, partly due to the presence of resistant cancer stem cells (CSCs) which are responsible of recurrences. CSCs have low EGFR expression and, conversely, overexpress the anti-apoptotic Bcl-2 protein, which is involved in resistance to apoptosis and the invasion/migration capacities of tumour cells.
The combination therapy of ABT-199, a Bcl-2 inhibitor, cetuximab an EGFR inhibitor, and radiation using an HNSCC model (SQ20B cell line) and its corresponding CSC subpopulation were evaluated in vitro (2D/3D cell proliferation; invasion/migration and apoptosis using videomicroscopy) and in vivo.
Cetuximab strongly inhibited 2D and 3D cell proliferation, as well as invasion/migration, only in non-CSC-SQ20B cells, whereas ABT-199 selectively inhibited these mechanisms in SQ20B/CSCs. The combination of irradiation + cetuximab + ABT-199 increased the inhibition of the 2D and 3D cell proliferation, invasion/migration, and resistance to apoptosis in both cell sub-populations. In addition, in a nude mouse model with heterotopic tumour xenograft, a treatment combining cetuximab + ABT-199 with fractional irradiation strongly delayed the tumour growth and increased in vivo lifespan without side effects.
Based on the present results, this triple combination therapy may represent a new opportunity for testing in clinical trials, particularly in locally advanced HNSCC.
头颈部鳞状细胞癌(HNSCC)的临床疗效仍然较差,部分原因是存在耐药性癌症干细胞(CSC),这些细胞是导致复发的原因。CSC 表达的表皮生长因子受体(EGFR)水平较低,相反,它们过度表达抗凋亡的 Bcl-2 蛋白,该蛋白参与肿瘤细胞的凋亡抵抗和侵袭/迁移能力。
我们评估了 Bcl-2 抑制剂 ABT-199、EGFR 抑制剂西妥昔单抗和放疗联合应用对头颈部鳞状细胞癌模型(SQ20B 细胞系)及其相应的 CSC 亚群的体外(2D/3D 细胞增殖;视频显微镜检测的侵袭/迁移和凋亡)和体内作用。
西妥昔单抗强烈抑制了非 CSC-SQ20B 细胞的 2D 和 3D 细胞增殖、侵袭/迁移,而 ABT-199 则选择性抑制了 SQ20B/CSCs 的这些机制。放疗联合西妥昔单抗和 ABT-199 增加了两种细胞亚群中 2D 和 3D 细胞增殖、侵袭/迁移和抗凋亡的抑制作用。此外,在带有异位肿瘤异种移植的裸鼠模型中,西妥昔单抗联合 ABT-199 与分次放疗的联合治疗强烈地延缓了肿瘤生长并增加了体内生存时间,且没有副作用。
基于目前的结果,这种三联疗法可能为临床试验提供新的机会,特别是在局部晚期 HNSCC 中。