TY - JOUR
T1 - The molecular landscape influencing prognoses of epithelial ovarian cancer
AU - Liu, Chao Lien
AU - Yuan, Ray Hwang
AU - Mao, Tsui Lien
N1 - Funding Information:
This work was supported in part by grants from the Ministry of Science and Technology, Taiwan to C.L.L (MOST 108-2314-B-038-059-MY3) and to T.L.M (MOST 106-2320-B-002-030-MY3).
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/7
Y1 - 2021/7
N2 - Epithelial ovarian cancer (EOC) is one of the major increasing lethal malignancies of the gynecological tract, mostly due to delayed diagnosis and chemoresistance, as well as its very heterogeneous genetic makeup. Application of high-throughput molecular technologies, gene expression microarrays, and powerful preclinical models has provided a deeper understanding of the molecular characteristics of EOC. Therefore, molecular markers have become a potent tool in EOC management, including prediction of aggressiveness, prognosis, and recurrence, and identification of novel therapeutic targets. In addition, biomarkers derived from genomic/epigenomic alterations (e.g., gene mutations, copy number aberrations, and DNA methylation) enable targeted treatment of affected signaling pathways in advanced EOC, thereby improving the effectiveness of traditional treatments. This review outlines the molecular landscape and discusses the impacts of biomarkers on the detection, diagnosis, surveillance, and therapeutic targets of EOC. These findings focus on the necessity to translate these potential biomarkers into clinical practice.
AB - Epithelial ovarian cancer (EOC) is one of the major increasing lethal malignancies of the gynecological tract, mostly due to delayed diagnosis and chemoresistance, as well as its very heterogeneous genetic makeup. Application of high-throughput molecular technologies, gene expression microarrays, and powerful preclinical models has provided a deeper understanding of the molecular characteristics of EOC. Therefore, molecular markers have become a potent tool in EOC management, including prediction of aggressiveness, prognosis, and recurrence, and identification of novel therapeutic targets. In addition, biomarkers derived from genomic/epigenomic alterations (e.g., gene mutations, copy number aberrations, and DNA methylation) enable targeted treatment of affected signaling pathways in advanced EOC, thereby improving the effectiveness of traditional treatments. This review outlines the molecular landscape and discusses the impacts of biomarkers on the detection, diagnosis, surveillance, and therapeutic targets of EOC. These findings focus on the necessity to translate these potential biomarkers into clinical practice.
KW - Biomarker
KW - Epithelial ovarian cancer (EOC)
KW - Genome/epigenome
KW - Mutation
KW - Personalized medicine
KW - Therapeutic targets
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U2 - 10.3390/biom11070998
DO - 10.3390/biom11070998
M3 - Review article
AN - SCOPUS:85109083516
SN - 2218-273X
VL - 11
JO - Biomolecules
JF - Biomolecules
IS - 7
M1 - 998
ER -