| Literature DB >> 32512900 |
Elena Alexandrova1, Giovanni Pecoraro1, Assunta Sellitto1, Viola Melone1, Carlo Ferravante1,2, Teresa Rocco1,2, Anna Guacci2, Giorgio Giurato1, Giovanni Nassa1, Francesca Rizzo1, Alessandro Weisz1,3, Roberta Tarallo1.
Abstract
Ovarian cancer (OC) shows the highest mortality rate among gynecological malignancies and, because of the absence of specific symptoms, it is frequently diagnosed at an advanced stage, mainly due to the lack of specific and early biomarkers, such as those based on cancer molecular signature identification. Indeed, although significant progress has been made toward improving the clinical outcome of other cancers, rates of mortality for OC are essentially unchanged since 1980, suggesting the need of new approaches to identify and characterize the molecular mechanisms underlying pathogenesis and progression of these malignancies. In addition, due to the low response rate and the high frequency of resistance to current treatments, emerging therapeutic strategies against OC focus on targeting single factors and pathways specifically involved in tumor growth and metastasis. To date, loss-of-function screenings are extensively applied to identify key drug targets in cancer, seeking for more effective, disease-tailored treatments to overcome lack of response or resistance to current therapies. We review here the information relative to essential genes and functional pathways recently discovered in OC, often strictly interconnected with each other and representing promising biomarkers and molecular targets to treat these malignancies.Entities:
Keywords: fitness genes; hub molecules; molecular signature; ovarian cancer
Year: 2020 PMID: 32512900 DOI: 10.3390/cancers12061470
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639