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Updated: Oct 20, 2025

Quantitative Mass Spectrometric Profiling of Cancer-cell Proteomes Derived From Liquid and Solid Tumors
Published on: February 27, 2015
Protein-gene Expression Nexus: Comprehensive characterization of human cancer cell lines with proteogenomic analysis
Daejin Hyung1, Min-Jeong Baek1, Jongkeun Lee1
1National Cancer Center, 323 Ilsan-ro, Goyang-si, Gyeonggi-do 10408, Republic of Korea.
Abstract:
Researchers have gained new therapeutic insights using multi-omics platform approaches to study DNA, RNA, and proteins of comprehensively characterized human cancer cell lines. To improve our understanding of the molecular features associated with oncogenic modulation in cancer, we proposed a proteogenomic database for human cancer cell lines, called Protein-gene Expression Nexus (PEN). We have expanded the characterization of cancer cell lines to include genetic, mRNA, and protein data of 145 cancer cell lines from various public studies. PEN contains proteomic and phosphoproteomic data on 4,129,728 peptides, 13,862 proteins, 7,138 phosphorylation site-associated genomic variations, 117 studies, and 12 cancer. We analyzed functional characterizations along with the integrated datasets, such as cis/trans association for copy number alteration (CNA), single amino acid variation for coding genes, post-translation modification site variation for Single Amino Acid Variation, and novel peptide expression for noncoding regions and fusion genes. PEN provides a user-friendly interface for searching, browsing, and downloading data and also supports the visualization of genome-wide association between CNA and expression, novel peptide landscape, mRNA-protein abundance, and functional annotation. Together, this dataset and PEN data portal provide a resource to accelerate cancer research using model cancer cell lines. PEN is freely accessible at http://combio.snu.ac.kr/pen.
Insights
Researchers developed the Protein-gene Expression Nexus (PEN), a proteogenomic database integrating multi-omics data from 145 cancer cell lines. This resource accelerates cancer research by providing insights into molecular features driving oncogenic modulation.
Area of Science:
- Cancer Research
- Proteogenomics
- Multi-omics
Background:
- Understanding molecular features of oncogenic modulation in cancer is crucial for therapeutic insights.
- Multi-omics approaches studying DNA, RNA, and proteins in human cancer cell lines offer new therapeutic avenues.
Purpose of the Study:
- To develop a comprehensive proteogenomic database for human cancer cell lines to enhance understanding of molecular features associated with oncogenic modulation.
- To integrate genetic, mRNA, and protein data from diverse cancer cell line studies.
Main Methods:
- Expanded characterization of 145 cancer cell lines with genetic, mRNA, and protein data from public studies.
- Compiled proteomic and phosphoproteomic data, including peptides, proteins, and phosphorylation site-associated genomic variations.
- Analyzed functional characterizations and integrated datasets, including copy number alteration (CNA), single amino acid variation, and post-translation modification site variation.
Main Results:
- The Protein-gene Expression Nexus (PEN) database integrates data from 117 studies across 12 cancer types.
- PEN contains extensive proteomic and phosphoproteomic data, encompassing millions of peptides and thousands of proteins and genomic variations.
- Functional analyses revealed associations between CNA, gene expression, and novel peptide expression.
Conclusions:
- The PEN database and data portal serve as a valuable resource for accelerating cancer research.
- Provides a user-friendly platform for data exploration, visualization, and download to facilitate discovery.
- Facilitates research on model cancer cell lines for improved therapeutic strategies.
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