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鉴定和评估 Aurora 激酶抑制剂 CCT137690 的新型药物组合,以增强口腔癌细胞的疗效。

Identification and evaluation of novel drug combinations of Aurora kinase inhibitor CCT137690 for enhanced efficacy in oral cancer cells.

机构信息

Department of Biology, Syed Babar Ali School of Science and Engineering, Lahore University of Management Sciences , Lahore , Pakistan.

Department of Chemistry & Chemical Engineering, Syed Babar Ali School of Science and Engineering, Lahore University of Management Sciences , Lahore , Pakistan.

出版信息

Cell Cycle. 2019 Sep;18(18):2281-2292. doi: 10.1080/15384101.2019.1643658. Epub 2019 Jul 26.

Abstract

Oral cancer is the most prevalent subtype of head and neck cancers and arises mainly from squamous cells of the oral cavity. Patients with advanced metastatic disease have poor overall survival resulting primarily from limited treatment options. Recent advances in the understanding of molecular basis of oral tumorigenesis provide an opportunity for identification and validation of new drug targets. The deregulated expression of the Aurora family of mitotic kinases, for example, has been associated with pathogenesis and poor prognosis in oral cancer. Here, we have evaluated the efficacy of the pan-Aurora inhibitor (CCT137690) alone and in combination with different chemotherapeutic and targeted drugs to identify its synergistic partners in oral cancer cell lines (ORL-48 and ORL-115). CCT137690 effectively inhibits Aurora kinases in both the cell lines and displays potent antiproliferative activity towards them. Prolonged treatment of these cells with CCT137690 results in abrogated mitotic spindle formation, misaligned chromosome attachment and polyploidy that ultimately leads to apoptotic cell death. We further identified that inhibitors of EGFR (gefitinib) and PI3-kinase (pictilisib) synergize with CCT137690 to inhibit the proliferation of the oral cancer cell lines. Moreover, we demonstrate that polyethylene glycol-based nanocapsules harboring combinations of CCT137690 with gefitinib or pictilisib inhibit the growth of oral cancer cell lines in 3D spheroid cultures and induce apoptosis that is comparable to free drug combinations. In conclusion, we have demonstrated the in vitro efficacy of CCT137690 in oral cancer cell lines, identified novel drug combinations with CCT137690 and synthesized nanocapsules containing these drug combinations for co-administration.

摘要

口腔癌是头颈部癌症中最常见的亚型,主要来源于口腔的鳞状细胞。晚期转移性疾病患者总体生存率较差,主要是因为治疗选择有限。近年来,对口腔肿瘤发生分子基础的认识的进步为识别和验证新的药物靶点提供了机会。例如,有丝分裂激酶 Aurora 家族的失调表达与口腔癌的发病机制和预后不良有关。在这里,我们评估了泛 Aurora 抑制剂(CCT137690)单独使用以及与不同化疗和靶向药物联合使用在口腔癌细胞系(ORL-48 和 ORL-115)中的疗效,以确定其协同伙伴。CCT137690 能有效地抑制这两个细胞系中的 Aurora 激酶,并对其显示出强大的抗增殖活性。这些细胞长期用 CCT137690 处理会导致有丝分裂纺锤体的形成被阻断,染色体附着错位和多倍体化,最终导致细胞凋亡死亡。我们进一步确定 EGFR(吉非替尼)和 PI3-激酶(pictilisib)抑制剂与 CCT137690 协同抑制口腔癌细胞系的增殖。此外,我们证明了载有 CCT137690 与吉非替尼或 pictilisib 组合的基于聚乙二醇的纳米胶囊在 3D 球体培养物中抑制口腔癌细胞系的生长,并诱导与游离药物组合相当的细胞凋亡。总之,我们已经证明了 CCT137690 在口腔癌细胞系中的体外疗效,确定了与 CCT137690 联合使用的新的药物组合,并合成了含有这些药物组合的纳米胶囊用于联合给药。

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