Codony-Servat Jordi, Cuatrecasas Miriam, Asensio Elena, Montironi Carla, Martínez-Cardús Anna, Marín-Aguilera Mercedes, Horndler Carlos, Martínez-Balibrea Eva, Rubini Michele, Jares Pedro, Reig Oscar, Victoria Iván, Gaba Lydia, Martín-Richard Marta, Alonso Vicente, Escudero Pilar, Fernández-Martos Carlos, Feliu Jaime, Méndez Jose Carlos, Méndez Miguel, Gallego Javier, Salud Antonieta, Rojo Federico, Castells Antoni, Prat Aleix, Rosell Rafael, García-Albéniz Xabier, Camps Jordi, Maurel Joan
Medical Oncology Department, Hospital Clínic, Translational Genomics and Targeted Therapeutics in Solid Tumors Group, IDIBAPS, Universitat de Barcelona, c/ Villarroel, 170, Barcelona 08036, Spain.
Medical Oncology Service, Institut Català d'Oncologia-Hospital Germans Trias i Pujol, Crta. de Canyet, s/n, Badalona 08916, Spain.
Br J Cancer. 2017 Dec 5;117(12):1777-1786. doi: 10.1038/bjc.2017.279. Epub 2017 Nov 9.
Although chemotherapy is the cornerstone treatment for patients with metastatic colorectal cancer (mCRC), acquired chemoresistance is common and constitutes the main reason for treatment failure. Monoclonal antibodies against insulin-like growth factor-1 receptor (IGF-1R) have been tested in pre-treated mCRC patients, but results have been largely deceiving.
We analysed time to progression, overall survival, and the mutational status of RAS, BRAF and nuclear p-IGF-1R expression by immunohistochemistry, in 470 metastatic CRC patients. The effect of IGF-1R activation and distribution was also assessed using cellular models of CRC and RNAi for functional validation.
Nuclear IGF-1R increased in metastatic tumours compared to paired untreated primary tumours, and significantly correlated with poor overall survival in mCRC patients. In vitro, chemo-resistant cell lines presented significantly higher levels of IGF-1R expression within the nuclear compartment, and PIAS3, a protein implicated also in the sumoylation process of intranuclear proteins, contributed to IGF-1R nuclear sequestration, highlighting the essential role of PIAS3 in this process. Intriguingly, we observed that ganitumab, an IGF-1R blocking-antibody used in several clinical trials, and dasatinib, an SRC inhibitor, increased the nuclear localisation of IGF-1R.
Our study demonstrates that IGF-1R nuclear location might lead to chemotherapy and targeted agent resistance.
尽管化疗是转移性结直肠癌(mCRC)患者的基石性治疗方法,但获得性化疗耐药很常见,是治疗失败的主要原因。抗胰岛素样生长因子-1受体(IGF-1R)单克隆抗体已在预处理的mCRC患者中进行了测试,但结果大多令人失望。
我们通过免疫组织化学分析了470例转移性结直肠癌患者的疾病进展时间、总生存期以及RAS、BRAF的突变状态和核p-IGF-1R表达情况。还使用结直肠癌细胞模型和RNAi评估了IGF-1R激活和分布的影响,以进行功能验证。
与配对的未经治疗的原发性肿瘤相比,转移性肿瘤中核IGF-1R增加,且与mCRC患者的总生存期差显著相关。在体外,化疗耐药细胞系在核区室中呈现出显著更高水平的IGF-1R表达,并且PIAS3(一种也参与核内蛋白质SUMO化过程的蛋白质)促成了IGF-1R的核隔离,突出了PIAS3在此过程中的重要作用。有趣的是,我们观察到在多项临床试验中使用的IGF-1R阻断抗体ganitumab和SRC抑制剂达沙替尼增加了IGF-1R的核定位。
我们的研究表明,IGF-1R的核定位可能导致化疗和靶向药物耐药。