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miRNA Expression May Have Implications for Immunotherapy in PDGFRA Mutant GISTs.
Ravegnini, Gloria; Nannini, Margherita; Indio, Valentina; Serrano, Cesar; Gorini, Francesca; Astolfi, Annalisa; Di Vito, Aldo; Morroni, Fabiana; Pantaleo, Maria Abbondanza; Hrelia, Patrizia; Angelini, Sabrina.
Afiliação
  • Ravegnini G; Department of Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.
  • Nannini M; Department of Specialized, Experimental and Diagnostic Medicine, Sant'Orsola-Malpighi Hospital, University of Bologna, Via Massarenti 9, 40138 Bologna, Italy.
  • Indio V; Division of Oncology, IRCCS Azienda Ospedaliero Universitaria di Bologna, 40138 Bologna, Italy.
  • Serrano C; Department of Veterinary Medical Sciences, University of Bologna, 40164 Ozzano, Italy.
  • Gorini F; Sarcoma Translational Research Laboratory, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron Hospital Campus, C/ Natzaret 115-117, 08035 Barcelona, Spain.
  • Astolfi A; Department of Medical Oncology, Vall d'Hebron University Hospital, P/Vall d'Hebron 119, 08035 Barcelona, Spain.
  • Di Vito A; Department of Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.
  • Morroni F; Department of Specialized, Experimental and Diagnostic Medicine, Sant'Orsola-Malpighi Hospital, University of Bologna, Via Massarenti 9, 40138 Bologna, Italy.
  • Pantaleo MA; Department of Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.
  • Hrelia P; Department of Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.
  • Angelini S; Department of Specialized, Experimental and Diagnostic Medicine, Sant'Orsola-Malpighi Hospital, University of Bologna, Via Massarenti 9, 40138 Bologna, Italy.
Int J Mol Sci ; 23(20)2022 Oct 14.
Article em En | MEDLINE | ID: mdl-36293105
Gastrointestinal stromal tumors (GISTs) harboring mutations in the PDGFRA gene occur in only about 5-7% of patients. The most common PDGFRA mutation is exon 18 D842V, which is correlated with specific clinico-pathological features compared to the other PDGFRA mutated GISTs. Herein, we present a miRNA expression profile comparison of PDGFRA D842V mutant GISTs and PDGFRA with mutations other than D842V (non-D842V). miRNA expression profiling was carried out on 10 patients using a TLDA miRNA array. Then, miRNA expression was followed by bioinformatic analysis aimed at evaluating differential expression, pathway enrichment, and miRNA-mRNA networks. We highlighted 24 differentially expressed miRNAs between D842V and non-D842V GIST patients. Pathway enrichment analysis showed that deregulated miRNAs targeted genes that are mainly involved in the immune response pathways. The miRNA-mRNA networks highlighted a signature of miRNAs/mRNA that could explain the indolent behavior of the D842V mutated GIST. The results highlighted a different miRNA fingerprint in PDGFRA D842V GISTs compared to non-D842Vmutated patients, which could explain the different biological behavior of this GIST subset.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: MicroRNAs / Tumores do Estroma Gastrointestinal Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: MicroRNAs / Tumores do Estroma Gastrointestinal Idioma: En Ano de publicação: 2022 Tipo de documento: Article