Mehmood Aamir, Nawab Sadia, Jin Yifan, Hassan Hesham, Kaushik Aman Chandra, Wei Dong-Qing
Department of Bioinformatics and Biological Statistics, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai 200240, P.R. China.
State Key Laboratory of Microbial Metabolism and School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, P.R. China.
ACS Pharmacol Transl Sci. 2023 Feb 24;6(3):399-409. doi: 10.1021/acsptsci.2c00212. eCollection 2023 Mar 10.
Breast cancer is one of the major causes of death in women worldwide. It is a diverse illness with substantial intersubject heterogeneity, even among individuals with the same type of tumor, and customized therapy has become increasingly important in this sector. Because of the clinical and physical variability of different kinds of breast cancers, multiple staging and classification systems have been developed. As a result, these tumors exhibit a wide range of gene expression and prognostic indicators. To date, no comprehensive investigation of model training procedures on information from numerous cell line screenings has been conducted together with radiation data. We used human breast cancer cell lines and drug sensitivity information from Cancer Cell Line Encyclopedia (CCLE) and Genomics of Drug Sensitivity in Cancer (GDSC) databases to scan for potential drugs using cell line data. The results are further validated through three machine learning approaches: Elastic Net, LASSO, and Ridge. Next, we selected top-ranked biomarkers based on their role in breast cancer and tested them further for their resistance to radiation using the data from the Cleveland database. We have identified six drugs named Palbociclib, Panobinostat, PD-0325901, PLX4720, Selumetinib, and Tanespimycin that significantly perform on breast cancer cell lines. Also, five biomarkers named TNFSF15, DCAF6, KDM6A, PHETA2, and IFNGR1 are sensitive to all six shortlisted drugs and show sensitivity to the radiations. The proposed biomarkers and drug sensitivity analysis are helpful in translational cancer studies and provide valuable insights for clinical trial design.
乳腺癌是全球女性主要死因之一。它是一种多样的疾病,即使在患有相同类型肿瘤的个体之间也存在显著的个体间异质性,因此定制化治疗在该领域变得越来越重要。由于不同类型乳腺癌的临床和物理变异性,已经开发了多种分期和分类系统。因此,这些肿瘤表现出广泛的基因表达和预后指标。迄今为止,尚未对来自众多细胞系筛选的信息与辐射数据一起进行模型训练程序的全面研究。我们使用来自癌症细胞系百科全书(CCLE)和癌症药物敏感性基因组学(GDSC)数据库的人类乳腺癌细胞系和药物敏感性信息,利用细胞系数据筛选潜在药物。结果通过三种机器学习方法进一步验证:弹性网络、套索回归和岭回归。接下来,我们根据生物标志物在乳腺癌中的作用选择排名靠前的生物标志物,并使用克利夫兰数据库的数据进一步测试它们对辐射的抗性。我们确定了六种名为帕博西尼、帕比司他、PD - 0325901、PLX4720、司美替尼和坦西莫司的药物,它们在乳腺癌细胞系上有显著效果。此外,五种名为TNFSF15、DCAF6、KDM6A、PHETA2和IFNGR1的生物标志物对所有六种入围药物敏感,并对辐射敏感。所提出的生物标志物和药物敏感性分析有助于转化癌症研究,并为临床试验设计提供有价值的见解。