RNA Sequencing-Based Identification of Ganglioside GD2-Positive Cancer Phenotype.
Maxim SorokinIrina V KholodenkoDaniel V KalinovskyTatyana ShamanskayaIgor DoroninDmitry KonovalovAleksei MironovDenis KuzminDaniil NikitinSergey DeyevAnton BuzdinRoman V KholodenkoPublished in: Biomedicines (2020)
The tumor-associated ganglioside GD2 represents an attractive target for cancer immunotherapy. GD2-positive tumors are more responsive to such targeted therapy, and new methods are needed for the screening of GD2 molecular tumor phenotypes. In this work, we built a gene expression-based binary classifier predicting the GD2-positive tumor phenotypes. To this end, we compared RNA sequencing data from human tumor biopsy material from experimental samples and public databases as well as from GD2-positive and GD2-negative cancer cell lines, for expression levels of genes encoding enzymes involved in ganglioside biosynthesis. We identified a 2-gene expression signature combining ganglioside synthase genes ST8SIA1 and B4GALNT1 that serves as a more efficient predictor of GD2-positive phenotype (Matthews Correlation Coefficient (MCC) 0.32, 0.88, and 0.98 in three independent comparisons) compared to the individual ganglioside biosynthesis genes (MCC 0.02-0.32, 0.1-0.75, and 0.04-1 for the same independent comparisons). No individual gene showed a higher MCC score than the expression signature MCC score in two or more comparisons. Our diagnostic approach can hopefully be applied for pan-cancer prediction of GD2 phenotypes using gene expression data.
Keyphrases
- gene expression
- papillary thyroid
- dna methylation
- genome wide
- poor prognosis
- bioinformatics analysis
- squamous cell
- healthcare
- genome wide identification
- big data
- computed tomography
- magnetic resonance imaging
- electronic health record
- squamous cell carcinoma
- drug delivery
- ionic liquid
- lymph node metastasis
- single molecule
- fine needle aspiration
- adverse drug
- contrast enhanced
- drug induced