Proteome- wide Tyrosine Phosphorylation Analysis Reveals Dysregulated Signaling Pathways in Ovarian Tumors

被引：20

作者：

Song, Guang ^{[1
]}

Chen, Li ^{[2
]}

Zhang, Bai ^{[2
]}

Song, Qifeng ^{[1
]}

Yu, Yu ^{[2
]}

Mooret, Cedric ^{[1
]}

Wang, Tian-Li ^{[2
,3
]}

Shih, Ie-Ming ^{[3
]}

Zhang, Hui ^{[2
]}

Chan, Daniel W. ^{[2
]}

Zhang, Zhen ^{[2
]}

Zhu, Heng ^{[1
]}

机构：

[1] Johns Hopkins Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA

[2] Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21231 USA

[3] Johns Hopkins Med Inst, Dept Gynecol & Obstet, Baltimore, MD 21231 USA

来源：

MOLECULAR & CELLULAR PROTEOMICS | 2019年 / 18卷 / 03期

关键词：

SRC FAMILY KINASES; FOCAL ADHESION KINASE; CELL-GROWTH; CANCER; TARGET; IDENTIFICATION; PROGRESSION; MICROARRAY; FAK;

D O I：

10.1074/mcp.RA118.000851

中图分类号：

Q5 [生物化学];

学科分类号：

071010 ; 081704 ;

摘要：

The recent accomplishment of comprehensive proteogenomic analysis of high-grade serous ovarian carcinoma (HGSOC) tissues reveals cancer associated molecular alterations were not limited to variations among DNA, and mRNA/protein expression, but are a result of complex reprogramming of signaling pathways/networks mediated by the protein and post-translational modification (PTM) interactomes. A systematic, multiplexed approach interrogating enzyme-substrate relationships in the context of PTMs is fundamental in understanding the dynamics of these pathways, regulation of cellular processes, and their roles in disease processes. Here, as part of Clinical Proteomic Tumor Analysis Consortium (CPTAC) project, we established a multiplexed PTM assay (tyrosine phosphorylation, and lysine acetylation, ubiquitylation and SUMOylation) method to identify protein probes' PTMs on the human proteome array. Further, we focused on the tyrosine phosphorylation and identified 19 kinases are potentially responsible for the dysregulated signaling pathways observed in HGSOC. Additionally, elevated kinase activity was observed when 14 ovarian cancer cell lines or tumor tissues were subjected to test the autophosphorylation status of PTK2 (pY397) and PTK2B (pY402) as a proxy for kinase activity. Taken together, this report demonstrates that PTM signatures based on lysate reactions on human proteome array is a powerful, unbiased approach to identify dysregulated PTM pathways in tumors.

引用

页码：448 / 460

页数：13

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