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Identification and Validation of HCC-specific Gene Transcriptional Signature for Tumor Antigen Discovery

A novel two-step bioinformatics strategy was applied for identification of signatures with therapeutic implications in hepatitis-associated HCC. Transcriptional profiles from HBV- and HCV-associated HCC samples were compared with non-tumor liver controls. Resulting HCC modulated genes were subsequen...

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Detalles Bibliográficos
Autores principales: Petrizzo, Annacarmen, Caruso, Francesca Pia, Tagliamonte, Maria, Tornesello, Maria Lina, Ceccarelli, Michele, Costa, Valerio, Aprile, Marianna, Esposito, Roberta, Ciliberto, Gennaro, Buonaguro, Franco M., Buonaguro, Luigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937235/
https://www.ncbi.nlm.nih.gov/pubmed/27387388
http://dx.doi.org/10.1038/srep29258
Descripción
Sumario:A novel two-step bioinformatics strategy was applied for identification of signatures with therapeutic implications in hepatitis-associated HCC. Transcriptional profiles from HBV- and HCV-associated HCC samples were compared with non-tumor liver controls. Resulting HCC modulated genes were subsequently compared with different non-tumor tissue samples. Two related signatures were identified, namely “HCC-associated” and “HCC-specific”. Expression data were validated by RNA-Seq analysis carried out on unrelated HCC samples and protein expression was confirmed according to The Human Protein Atlas" (http://proteinatlas.org/), a public repository of immunohistochemistry data. Among all, aldo-keto reductase family 1 member B10, and IGF2 mRNA-binding protein 3 were found strictly HCC-specific with no expression in 18/20 normal tissues. Target peptides for vaccine design were predicted for both proteins associated with the most prevalent HLA-class I and II alleles. The described novel strategy showed to be feasible for identification of HCC-specific proteins as highly potential target for HCC immunotherapy.