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Cultured isolates will not only expand the reference genome databases, they may also reveal novel genes/functions for development of new therapeutics

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Conclusion CR dramatically reduces immune responses, dysregulates tissue-specific epithelial stem cell developmental processes and telomere maintaining processes CR induces metabolic reprogramming processes, oncogenic and cell cycle pathways, and may increase the risk of malignancy CR-induced Rrm2, Lamc2, Fkbp5, and aberrant glutathione gene family activation coupled with Sirtuin3 and RNaseL suppression could play tumorigenic roles in mucosa pathophysiology Interferon-inducible gene family including novel members on Chr11qB1.2 are suppressed by CR Data Availability The microarray datasets analyzed during the current study are available in the ArrayExpress repository, Authors contributions Concept, design and study supervision: V.A.K., Development of methodology, analysis and interpretation of results and writing of manuscript: E.M, V.A.K