| Literature DB >> 34207450 |
Mihaela Raluca Radu1, Alina Prădatu1, Florentina Duică1, Romeo Micu2, Sanda Maria Creţoiu3, Nicolae Suciu1,4,5, Dragoş Creţoiu1,3, Valentin Nicolae Varlas6,7, Viorica Elena Rădoi5,8.
Abstract
Ovarian cancer is one of the most common causes of death in women as survival is highly dependent on the stage of the disease. Ovarian cancer is typically diagnosed in the late stage due to the fact that in the early phases is mostly asymptomatic. Genomic instability is one of the hallmarks of ovarian cancer. While ovarian cancer is stratified into different clinical subtypes, there still exists extensive genetic and progressive diversity within each subtype. Early detection of the disorder is one of the most important steps that facilitate a favorable prognosis and a good response to medical therapy for the patients. In targeted therapies, individual patients are treated by agents targeting the changes in tumor cells that help them grow, divide and spread. Currently, in gynecological malignancies, potential therapeutic targets include tumor-intrinsic signaling pathways, angiogenesis, homologous-recombination deficiency, hormone receptors, and immunologic factors. Ovarian cancer is usually diagnosed in the final stages, partially due to the absence of an effective screening strategy, although, over the times, numerous biomarkers have been studied and used to assess the status, progression, and efficacy of the drug therapy in this type of disorder.Entities:
Keywords: NTRK inhibitors; PARP inhibitors; biomarkers; ncRNAs; ovarian cancer; targeted therapy
Year: 2021 PMID: 34207450 DOI: 10.3390/biomedicines9060693
Source DB: PubMed Journal: Biomedicines ISSN: 2227-9059