Journal
CANCERS
Volume 15, Issue 11, Pages -Publisher
MDPI
DOI: 10.3390/cancers15112990
Keywords
ovarian cancer; germ cell tumors; genomics; epigenomics; pediatric and adult
Categories
Ask authors/readers for more resources
Because ovarian germ cell tumors (OGCTs) are rare, our understanding of them is limited due to insufficient studies on their molecular basis in pediatric and adult cancers. This paper provides an overview of the etiology and pathogenesis of OGCTs in children and adults, focusing on their molecular characteristics.
Simple Summary: Because ovarian germ cell tumors (OGCTs) are rare tumors, our current understanding of them is sparse; this is because few studies have investigated the molecular basis of pediatric and adult cancers. In this paper, we aim to provide an overview of the etiopathogenesis of OGCTs in children and adults, and we address the molecular landscape of these tumors.Ovarian germ cell tumors (OGCTs) are rare in adults; indeed, they occur predominantly in children, adolescents, and young adults, and they account for approximately 11% of cancer diagnoses in these groups. Because OGCTs are rare tumors, our current understanding of them is sparse; this is because few studies have investigated the molecular basis of pediatric and adult cancers. Here, we review the etiopathogenesis of OGCTs in children and adults, and we address the molecular landscape of these tumors, including integrated genomic analysis, microRNAs, DNA methylation, the molecular implications of treatment resistance, and the development of in vitro and in vivo models. An elucidation of potential molecular alterations may provide a novel field for understanding the pathogenesis, tumorigenesis, diagnostic markers, and genetic peculiarity of the rarity and complexity of OGCTs.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available