Phosphorylated ribosomal S6 (p-rpS6) as a post-treatment indicator of HER2 signalling targeted drug resistance

被引:11
作者
Yang-Kolodji, Gloria [1 ]
Mumenthaler, Shannon M. [2 ]
Mehta, Arjun [1 ]
Ji, Lingyun [3 ]
Tripathy, Debu [1 ,4 ]
机构
[1] Univ So Calif, Dept Med, Kenneth Norris Jr Comprehens Canc Ctr, Los Angeles, CA 90033 USA
[2] Univ So Calif, Ctr Appl Mol Med, Los Angeles, CA 90033 USA
[3] Univ So Calif, Dept Prevent Med, Kenneth Norris Jr Comprehens Canc Ctr, Los Angeles, CA 90033 USA
[4] Univ Texas Houston, MD Anderson Canc Ctr, Houston, TX USA
关键词
Biomarker; breast cancer; cell model; drug response; trastuzumab resistance; METASTATIC BREAST-CANCER; OVERCOMING RESISTANCE; PARADIGM-SHIFT; SINGLE-AGENT; TRASTUZUMAB; LAPATINIB; SURVIVAL; EFFICACY; SAFETY; KI67;
D O I
10.3109/1354750X.2015.1068865
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Objective: To identify clinically relevant predictive biomarkers of trastuzumab resistance. Material and methods: MTT, FACS assays, immunoblotting and immunocytochemistry were used to phenotypically characterize drug responses of two cell models BT474R and SKBR3R. Student's t-test and Spearman's correlation were applied for statistic analysis. Results: The activity of a downstream effector of the HER2 pathway phosphorylated ribosomal protein S6 (p-rpS6), was suppressed by trastuzumab in the parental cell lines yet remained unchanged in the resistant cells following treatment. The level of p-rpS6 was inversely correlated to the drug induced growth inhibition of trastuzumab-resistant cells when they are treated with selected HER2 targeting drugs. Conclusion: p-rpS6 is a robust post-treatment indicator of HER2 pathway-targeted therapy resistance.
引用
收藏
页码:313 / 322
页数:10
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