Emerging power of proteomics for delineation of intrinsic tumor subtypes and resistance mechanisms to anti-cancer therapies

被引:0
作者
Oh, Sejin [1 ]
Kim, Hyun Seok [1 ]
机构
[1] Yonsei Univ, Coll Med, Severance Biomed Sci Inst, Brain Korea Project Med Sci 21, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Tumor subtype; drug resistance; quantitative proteomics; multi-omics; cancer heterogeneity; PHASE PROTEIN ARRAYS; BREAST-CANCER; QUANTITATIVE PROTEOMICS; MOLECULAR CLASSIFICATION; SYSTEMATIC IDENTIFICATION; MESENCHYMAL TRANSITION; SIGNALING PATHWAYS; GASTRIC-CANCER; CELL-LINES; INHIBITION;
D O I
10.1080/14789450.2016.1233063
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Despite extreme genetic heterogeneity, tumors often show similar alterations in the expression, stability, and activation of proteins important in oncogenic signaling pathways. Thus, classifying tumor samples according to shared proteomic features may help facilitate the identification of cancer subtypes predictive of therapeutic responses and prognostic for patient outcomes. Meanwhile, understanding mechanisms of intrinsic and acquired resistance to anti-cancer therapies at the protein level may prove crucial to devising reversal strategies.Areas covered: Herein, we review recent advances in quantitative proteomic technology and their applications in studies to identify intrinsic tumor subtypes of various tumors, to illuminate mechanistic aspects of pharmacological and oncogenic adaptations, and to highlight interaction targets for anti-cancer compounds and cancer-addicted proteins.Expert commentary: Quantitative proteomic technologies are being successfully employed to classify tumor samples into distinct intrinsic subtypes, to improve existing DNA/RNA based classification methods, and to evaluate the activation status of key signaling pathways.
引用
收藏
页码:929 / 939
页数:11
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