Phosphoproteomics identifies oncogenic Ras signaling targets and their involvement in lung adenocarcinomas.

BACKGROUND:Ras is frequently mutated in a variety of human cancers, including lung cancer, leading to constitutive activation of MAPK signaling. Despite decades of research focused on the Ras oncogene, Ras-targeted phosphorylation events and signaling pathways have not been described on a proteome-w...

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Main Authors: Putty-Reddy Sudhir, Chia-Lang Hsu, Mei-Jung Wang, Yi-Ting Wang, Yu-Ju Chen, Ting-Yi Sung, Wen-Lian Hsu, Ueng-Cheng Yang, Jeou-Yuan Chen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3102680?pdf=render
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author Putty-Reddy Sudhir
Chia-Lang Hsu
Mei-Jung Wang
Yi-Ting Wang
Yu-Ju Chen
Ting-Yi Sung
Wen-Lian Hsu
Ueng-Cheng Yang
Jeou-Yuan Chen
author_facet Putty-Reddy Sudhir
Chia-Lang Hsu
Mei-Jung Wang
Yi-Ting Wang
Yu-Ju Chen
Ting-Yi Sung
Wen-Lian Hsu
Ueng-Cheng Yang
Jeou-Yuan Chen
author_sort Putty-Reddy Sudhir
collection DOAJ
description BACKGROUND:Ras is frequently mutated in a variety of human cancers, including lung cancer, leading to constitutive activation of MAPK signaling. Despite decades of research focused on the Ras oncogene, Ras-targeted phosphorylation events and signaling pathways have not been described on a proteome-wide scale. METHODOLOGY/PRINCIPAL FINDINGS:By functional phosphoproteomics, we studied the molecular mechanics of oncogenic Ras signaling using a pathway-based approach. We identified Ras-regulated phosphorylation events (n = 77) using label-free comparative proteomics analysis of immortalized human bronchial epithelial cells with and without the expression of oncogenic Ras. Many were newly identified as potential targets of the Ras signaling pathway. A majority (∼60%) of the Ras-targeted events consisted of a [pSer/Thr]-Pro motif, indicating the involvement of proline-directed kinases. By integrating the phosphorylated signatures into the Pathway Interaction Database, we further inferred Ras-regulated pathways, including MAPK signaling and other novel cascades, in governing diverse functions such as gene expression, apoptosis, cell growth, and RNA processing. Comparisons of Ras-regulated phosphorylation events, pathways, and related kinases in lung cancer-derived cells supported a role of oncogenic Ras signaling in lung adenocarcinoma A549 and H322 cells, but not in large cell carcinoma H1299 cells. CONCLUSIONS/SIGNIFICANCE:This study reveals phosphorylation events, signaling networks, and molecular functions that are regulated by oncogenic Ras. The results observed in this study may aid to extend our knowledge on Ras signaling in lung cancer.
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spelling doaj.art-39e679470b7f4ee1a600bd39888cfb112022-12-21T23:04:53ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0165e2019910.1371/journal.pone.0020199Phosphoproteomics identifies oncogenic Ras signaling targets and their involvement in lung adenocarcinomas.Putty-Reddy SudhirChia-Lang HsuMei-Jung WangYi-Ting WangYu-Ju ChenTing-Yi SungWen-Lian HsuUeng-Cheng YangJeou-Yuan ChenBACKGROUND:Ras is frequently mutated in a variety of human cancers, including lung cancer, leading to constitutive activation of MAPK signaling. Despite decades of research focused on the Ras oncogene, Ras-targeted phosphorylation events and signaling pathways have not been described on a proteome-wide scale. METHODOLOGY/PRINCIPAL FINDINGS:By functional phosphoproteomics, we studied the molecular mechanics of oncogenic Ras signaling using a pathway-based approach. We identified Ras-regulated phosphorylation events (n = 77) using label-free comparative proteomics analysis of immortalized human bronchial epithelial cells with and without the expression of oncogenic Ras. Many were newly identified as potential targets of the Ras signaling pathway. A majority (∼60%) of the Ras-targeted events consisted of a [pSer/Thr]-Pro motif, indicating the involvement of proline-directed kinases. By integrating the phosphorylated signatures into the Pathway Interaction Database, we further inferred Ras-regulated pathways, including MAPK signaling and other novel cascades, in governing diverse functions such as gene expression, apoptosis, cell growth, and RNA processing. Comparisons of Ras-regulated phosphorylation events, pathways, and related kinases in lung cancer-derived cells supported a role of oncogenic Ras signaling in lung adenocarcinoma A549 and H322 cells, but not in large cell carcinoma H1299 cells. CONCLUSIONS/SIGNIFICANCE:This study reveals phosphorylation events, signaling networks, and molecular functions that are regulated by oncogenic Ras. The results observed in this study may aid to extend our knowledge on Ras signaling in lung cancer.http://europepmc.org/articles/PMC3102680?pdf=render
spellingShingle Putty-Reddy Sudhir
Chia-Lang Hsu
Mei-Jung Wang
Yi-Ting Wang
Yu-Ju Chen
Ting-Yi Sung
Wen-Lian Hsu
Ueng-Cheng Yang
Jeou-Yuan Chen
Phosphoproteomics identifies oncogenic Ras signaling targets and their involvement in lung adenocarcinomas.
PLoS ONE
title Phosphoproteomics identifies oncogenic Ras signaling targets and their involvement in lung adenocarcinomas.
title_full Phosphoproteomics identifies oncogenic Ras signaling targets and their involvement in lung adenocarcinomas.
title_fullStr Phosphoproteomics identifies oncogenic Ras signaling targets and their involvement in lung adenocarcinomas.
title_full_unstemmed Phosphoproteomics identifies oncogenic Ras signaling targets and their involvement in lung adenocarcinomas.
title_short Phosphoproteomics identifies oncogenic Ras signaling targets and their involvement in lung adenocarcinomas.
title_sort phosphoproteomics identifies oncogenic ras signaling targets and their involvement in lung adenocarcinomas
url http://europepmc.org/articles/PMC3102680?pdf=render
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