Over the last decade, next-generation sequencing technologies have improved our ability to assess biological aspects, at genomic and transcriptomic levels, on a large scale— and have been increasingly used for the management of adult cancers. However, their efficacy and feasibility within pediatrics is still under investigation. “Omic” approaches represent an opportunity to understand the oncogenic mechanisms driving the onset and progression of bone sarcoma and improve the clinical management of young patients with bone sarcomas. This review focuses on the current genomic and transcriptomic characteristics of managing pediatric patients, affected by Ewing sarcoma and osteosarcoma.

Omic approaches to pediatric bone sarcomas

Cereda M.;Quarello P.;Fagioli F.
2020-01-01

Abstract

Over the last decade, next-generation sequencing technologies have improved our ability to assess biological aspects, at genomic and transcriptomic levels, on a large scale— and have been increasingly used for the management of adult cancers. However, their efficacy and feasibility within pediatrics is still under investigation. “Omic” approaches represent an opportunity to understand the oncogenic mechanisms driving the onset and progression of bone sarcoma and improve the clinical management of young patients with bone sarcomas. This review focuses on the current genomic and transcriptomic characteristics of managing pediatric patients, affected by Ewing sarcoma and osteosarcoma.
2020
67
2
e28072
e28079
Ewing sarcoma; genomic; next-generation sequencing; osteosarcoma; pediatric oncology; transcriptomic; Biomarkers, Tumor; Bone Neoplasms; Genomics; Humans; Osteosarcoma; Sarcoma, Ewing; Transcriptome
Tirtei E.; Cereda M.; De Luna E.; Quarello P.; Asaftei S.D.; Fagioli F.
File in questo prodotto:
File Dimensione Formato  
2020 OMIC_Tirtei.pdf

Accesso riservato

Tipo di file: PDF EDITORIALE
Dimensione 296.09 kB
Formato Adobe PDF
296.09 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1757670
Citazioni
  • ???jsp.display-item.citation.pmc??? 8
  • Scopus 13
  • ???jsp.display-item.citation.isi??? 12
social impact