Publicação: Integrated miRNA and mRNA expression analysis uncovers drug targets in laryngeal squamous cell carcinoma patients
dc.contributor.author | Lapa, Rainer Marco Lopez [UNESP] | |
dc.contributor.author | Barros-Filho, Mateus Camargo | |
dc.contributor.author | Marchi, Fabio Albuquerque | |
dc.contributor.author | Domingues, Maria Aparecida Custódio [UNESP] | |
dc.contributor.author | de Carvalho, Genival Barbosa | |
dc.contributor.author | Drigo, Sandra Aparecida [UNESP] | |
dc.contributor.author | Kowalski, Luiz Paulo | |
dc.contributor.author | Rogatto, Silvia Regina [UNESP] | |
dc.contributor.institution | CIPE – A.C.Camargo Cancer Center | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.contributor.institution | A.C.Camargo Cancer Center | |
dc.contributor.institution | University of Southern Denmark | |
dc.date.accessioned | 2019-10-06T16:27:20Z | |
dc.date.available | 2019-10-06T16:27:20Z | |
dc.date.issued | 2019-06-01 | |
dc.description.abstract | Objectives: The current treatment of laryngeal squamous cell carcinoma (LSCC)is based on radical surgery and radiotherapy resulting in high morbidity. Chemoradiotherapy has been used as alternative to organ sparing; however, several advanced cases presented resistance to treatment, which contributes to a high risk of recurrence and mortality. Coding RNAs and miRNAs have potential to be used as biomarkers or targets for cancer therapy. Materials and Methods: In this study, 36 LSCC and 5 non-neoplastic control samples were investigated using miRNA and mRNA large-scale expression analysis and a cross-validation was performed using the TCGA database (116 LSCC and 12 surrounding normal tissues). Results: The large-scale profiling revealed the involvement of 28 miRNAs and 817 genes differentially expressed in LSCC. An integrative analysis comprising predicted and experimentally validated miRNA/mRNA interactions (negatively correlated), resulted in 28 miRNAs and 543 mRNAs. Decreased expression of miR-199b was significantly associated with shorter disease-free survival in LSCC (internal and TCGA datasets). The expression levels of selected miRNAs (miR-199b-5p, miR-29c-3p, miR-204-5p, miR-125b-5p and miR-92a-3p)and genes (COL3A1, COL10A1, ERBB4, HMGA2, HLF, TOP2A, MMP3, MMP13, MMP10 and PPP1R3)were confirmed as altered in LSCC by RT-qPCR. Additionally, a drug target prediction analysis revealed drug combinations based on miRNA and mRNA expression, pointing out novel alternatives to optimize the LSCC treatment. Conclusion: Collectively, these findings provide new insights in the LSCC transcriptional deregulation and potential drug targets. | en |
dc.description.affiliation | International Research Center CIPE – A.C.Camargo Cancer Center | |
dc.description.affiliation | Department of Genetics Institute of Bioscience São Paulo State University – UNESP | |
dc.description.affiliation | Department of Pathology Faculty of Medicine São Paulo State University-UNESP | |
dc.description.affiliation | Department of Head and Neck Surgery and Otorhinolaryngology A.C.Camargo Cancer Center | |
dc.description.affiliation | Department of Surgery and Orthopedics Faculty of Medicine São Paulo State University - UNESP | |
dc.description.affiliation | Department of Clinical Genetics Vejle Hospital Institute of Regional Health Research University of Southern Denmark | |
dc.description.affiliationUnesp | Department of Genetics Institute of Bioscience São Paulo State University – UNESP | |
dc.description.affiliationUnesp | Department of Pathology Faculty of Medicine São Paulo State University-UNESP | |
dc.description.affiliationUnesp | Department of Surgery and Orthopedics Faculty of Medicine São Paulo State University - UNESP | |
dc.description.sponsorship | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description.sponsorshipId | CNPq: 153142/2012-0 | |
dc.description.sponsorshipId | FAPESP: 2008/57887-9 | |
dc.description.sponsorshipId | CNPq: 573589/08-9 | |
dc.format.extent | 76-84 | |
dc.identifier | http://dx.doi.org/10.1016/j.oraloncology.2019.04.018 | |
dc.identifier.citation | Oral Oncology, v. 93, p. 76-84. | |
dc.identifier.doi | 10.1016/j.oraloncology.2019.04.018 | |
dc.identifier.issn | 1879-0593 | |
dc.identifier.issn | 1368-8375 | |
dc.identifier.lattes | 0585723113037140 | |
dc.identifier.scopus | 2-s2.0-85064731170 | |
dc.identifier.uri | http://hdl.handle.net/11449/189023 | |
dc.language.iso | eng | |
dc.relation.ispartof | Oral Oncology | |
dc.rights.accessRights | Acesso aberto | |
dc.source | Scopus | |
dc.subject | Chemotherapy | |
dc.subject | Drug targets | |
dc.subject | Integrative analysis | |
dc.subject | Laryngeal squamous cell carcinoma | |
dc.subject | miRNAs | |
dc.subject | mRNA | |
dc.subject | Treatment | |
dc.title | Integrated miRNA and mRNA expression analysis uncovers drug targets in laryngeal squamous cell carcinoma patients | en |
dc.type | Artigo | |
dspace.entity.type | Publication | |
unesp.author.lattes | 0585723113037140 | |
unesp.campus | Universidade Estadual Paulista (Unesp), Faculdade de Medicina, Botucatu | pt |
unesp.department | Cirurgia e Ortopedia - FMB | pt |