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Computational Advances in the Label-free Quantification of Cancer Proteomics Data
Jing Tang1,2, Yang Zhang1,2, Jianbo Fu2
1School of Pharmaceutical Sciences, Chongqing University, Chongqing 401331, China.
Current Pharmaceutical Design
|November 3, 2018
Summary
Label-free quantification (LFQ) in cancer proteomics faces challenges in precision and reproducibility. This review analyzes computational advances to improve LFQ performance for discovering anticancer targets and drugs.
Area of Science:
- Proteomics
- Cancer Research
- Computational Biology
Background:
- Proteomics offers quantitative insights into tumor development and drug responses.
- It aids in identifying cancer targets and developing novel anticancer drugs.
- Characterizing protein expression is crucial for understanding malignancy.
Purpose of the Study:
- To systematically review and analyze computational advances in label-free quantification (LFQ) for cancer proteomics.
- To address the key technical challenges of low precision, poor reproducibility, and inaccuracy in LFQ.
- To enhance the discovery of anticancer targets and drugs.
Main Methods:
- Searched PubMed and Web of Science databases.
- Focused on label-free quantification approaches, cancer proteomics, and computational advances.
- Systematically reviewed and critically assessed acquisition techniques and quantification tools.
Main Results:
- Discussed various popular acquisition techniques and state-of-the-art quantification tools.
- Evaluated processing approaches (transformation, normalization, filtering, imputation) for improving LFQ performance.
- Proposed future directions for enhancing computation-based quantification in cancer proteomics.
Conclusions:
- There has been a dramatic increase in LFQ approaches in recent years.
- These advances significantly enhance quantification strategies for cancer proteomics.
- Improved computational methods are vital for advancing cancer drug discovery.
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