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阿哌利西(PI3K抑制剂)与瑞博西尼(CDK4/6抑制剂)联合应用在临床前结直肠癌模型中的协同作用

Synergistic Effects of the Combination of Alpelisib (PI3K Inhibitor) and Ribociclib (CDK4/6 Inhibitor) in Preclinical Colorectal Cancer Models.

作者信息

Aslam Razia, Richards Cathy E, Fay Joanna, Hudson Lance, Workman Julie, Lee Cha Len, Murphy Adrian, O'Neill Brian, Toomey Sinead, Hennessy Bryan T

机构信息

Medical Oncology Group, Department of Medicine, RCSI University of Medicine and Health Sciences, D09 YD60 Dublin, Ireland.

Beaumont RCSI Cancer Centre, D09 YD60 Dublin, Ireland.

出版信息

Int J Mol Sci. 2024 Dec 10;25(24):13264. doi: 10.3390/ijms252413264.

Abstract

The CDK4/6 inhibitor Ribociclib has shown limited efficacy as a monotherapy in colorectal cancer (CRC). However, combining Ribociclib with targeted therapies could present a viable strategy for treating CRC. This study evaluated the combination of Ribociclib and the PI3K inhibitor Alpelisib across four distinct cell lines representing different mutational statuses ( wild-type, -mutated, -mutated, and -mutated). We analyzed the drugs' impact on key proteins involved in the PI3K pathway, cell cycle regulation, and apoptosis. The combination of Alpelisib and Ribociclib demonstrated a synergistic anti-proliferative effect across all cell lines, leading to a simultaneous decrease in pRB, pAKT, and p-S6 levels, and a more comprehensive suppression of the PI3K/AKT/mTOR pathway. Additionally, there was an upregulation of the apoptotic marker, p-BCL2, in cells treated with the combination compared to controls. In vivo studies using Caco-2, LS1034, and SNUC4 xenografts revealed a significant reduction in tumour growth with the combination therapy compared to single-agent treatments. These findings suggest that combining Alpelisib and Ribociclib could be a promising therapeutic approach for CRC, warranting further clinical exploration.

摘要

细胞周期蛋白依赖性激酶4/6(CDK4/6)抑制剂瑞博西尼在结直肠癌(CRC)单药治疗中显示出有限的疗效。然而,将瑞博西尼与靶向疗法联合使用可能是一种治疗CRC的可行策略。本研究评估了瑞博西尼与磷脂酰肌醇-3-激酶(PI3K)抑制剂阿培利司在四种代表不同突变状态(野生型、 突变型、 突变型和 突变型)的不同细胞系中的联合应用。我们分析了这些药物对PI3K通路、细胞周期调控和细胞凋亡中关键蛋白的影响。阿培利司和瑞博西尼的联合应用在所有细胞系中均表现出协同抗增殖作用,导致视网膜母细胞瘤蛋白(pRB)、磷酸化蛋白激酶B(pAKT)和磷酸化核糖体蛋白S6(p-S6)水平同时降低,并对PI3K/AKT/哺乳动物雷帕霉素靶蛋白(mTOR)通路产生更全面的抑制。此外,与对照组相比,联合治疗的细胞中凋亡标志物磷酸化B细胞淋巴瘤-2(p-BCL2)上调。使用人结肠腺癌细胞系(Caco-2)、人结肠癌细胞系(LS1034)和人结肠癌细胞系(SNUC4)异种移植物进行的体内研究表明,与单药治疗相比,联合治疗显著降低了肿瘤生长。这些发现表明,阿培利司和瑞博西尼联合应用可能是一种有前景的CRC治疗方法,值得进一步的临床探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7894/11676898/4bcf9f2189cd/ijms-25-13264-g001.jpg

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