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CC-223抑制人头颈部鳞状细胞癌细胞生长。

CC-223 inhibits human head and neck squamous cell carcinoma cell growth.

作者信息

Wang Jun-Ying, Jin Xin, Zhang Xin, Li Xiao-Feng

机构信息

Department of ENT, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, China.

Department of Ophthalmology, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, China.

出版信息

Biochem Biophys Res Commun. 2018 Feb 19;496(4):1191-1196. doi: 10.1016/j.bbrc.2018.01.168. Epub 2018 Jan 31.

Abstract

mTOR over-activation is associated with the progression of head and neck squamous cell carcinoma (HNSCC). CC-223 is a novel and potent mTOR kinase inhibitor. Its activity against human HNSCC cells is studied here. In established SCC-9 cells and primary human oral cavity carcinoma (OCC) cells, CC-223 treatment at only nM concentrations significantly inhibited survival, proliferation and cell cycle progression. Furthermore, CC-223 provoked apoptosis activation in human HNSCC cells. CC-223 is more efficient in killing HNSCC cells than other known Akt-mTOR inhibitors: RAD001, MK-2206 and AZD-2014. CC-223 was however non-cytotoxic to the primary human oral epithelial cells. Further studies demonstrate that CC-223 almost completely blocked mTOR complex 1 (mTORC1) and mTORC2 activation in SCC-9 cells and primary OCC cells. In vivo, oral administration of CC-223 at well-tolerated doses potently inhibited SCC-9 xenograft tumor growth in severe combined immunodeficient mice. mTORC1 and mTORC2 activation was largely inhibited in CC-223-treated tumor tissues. Overall, targeting the mTOR kinase by CC-223 inhibits human HNSCC cell growth in vitro and in vivo. CC-223 might have a translational value for the treatment of HNSCC.

摘要

mTOR过度激活与头颈部鳞状细胞癌(HNSCC)的进展相关。CC-223是一种新型强效mTOR激酶抑制剂。本文研究了其对人HNSCC细胞的活性。在已建立的SCC-9细胞和原代人口腔癌细胞(OCC)中,仅以纳摩尔浓度的CC-223处理就能显著抑制细胞存活、增殖和细胞周期进程。此外,CC-223可激发人HNSCC细胞的凋亡激活。与其他已知的Akt-mTOR抑制剂(RAD001、MK-2206和AZD-2014)相比,CC-223在杀死HNSCC细胞方面更有效。然而,CC-223对原代人口腔上皮细胞无细胞毒性。进一步研究表明,CC-223几乎完全阻断了SCC-9细胞和原代OCC细胞中mTOR复合物1(mTORC1)和mTORC2的激活。在体内,以耐受性良好的剂量口服CC-223可有效抑制严重联合免疫缺陷小鼠中SCC-9异种移植瘤的生长。在CC-223处理的肿瘤组织中,mTORC1和mTORC2的激活受到很大抑制。总体而言,CC-223靶向mTOR激酶可在体外和体内抑制人HNSCC细胞生长。CC-223可能对HNSCC的治疗具有转化价值。

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