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Updated: Mar 12, 2026

Quantitative Mass Spectrometric Profiling of Cancer-cell Proteomes Derived From Liquid and Solid Tumors
Published on: February 27, 2015
Sample preparation method considerations for integrated transcriptomic and proteomic analysis of tumors.
Anupama Rajan Bhat1, Manoj Kumar Gupta2,3, Priya Krithivasan4
1Strand Life Sciences, Bangalore, India.
For integrated tumor analysis, Method 1, which isolates RNA and protein from a single tissue section, shows higher concordance in differential gene and protein expression compared to Method 2. This method is recommended for multiomics studies.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Integrated multiomics analysis of tumors requires compatible RNA and protein recovery protocols.
- Tumor heterogeneity can impact transcriptomic and proteomic data consistency.
Purpose of the Study:
- To compare two RNA and protein isolation methods for multiomics analysis of tumor tissues.
- To determine the optimal method for preserving transcriptomic and proteomic concordance.
Main Methods:
- Comparison of sequential (Method 1) versus parallel (Method 2) RNA and protein extraction from laryngopharyngeal tumor tissues.
- RNA sequencing (RNA-seq) and iTRAQ-based LC-MS/MS analysis of extracted samples.
Main Results:
- Method 1 yielded a higher number of concordant differentially expressed transcripts and proteins compared to Method 2.
- Sequential extraction from a single tissue section (Method 1) captured more concordant entities, highlighting tissue heterogeneity.
Conclusions:
- Method 1, involving sequential RNA and protein isolation from the same tissue section, is superior for integrated transcriptome and proteome analysis.
- This method enhances the reliability of multiomics data by accounting for molecular distribution heterogeneity.
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