Ravegnini Gloria, De Iaco Pierandrea, Gorini Francesca, Dondi Giulia, Klooster Isabella, De Crescenzo Eugenia, Bovicelli Alessandro, Hrelia Patrizia, Perrone Anna Myriam, Angelini Sabrina
Department of Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.
Division of Oncologic Gynecology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.
Biomedicines. 2021 Sep 26;9(10):1316. doi: 10.3390/biomedicines9101316.
Epithelial ovarian cancer (EOC) is one of the most lethal cancers worldwide, mostly due to nonspecific symptoms and a lack of screening tests, which, taken together, contribute to delayed diagnosis and treatment. The current clinical biomarker is serum CA-125, which allows the identification of most advanced primary and relapsed disease and correlates with disease burden; however, as well highlighted in the literature, CA-125 often lacks sensitivity and specificity, and is not helpful in monitoring chemotherapeutic response or in predicting the risk of relapse. Given that, the identification of novel biomarkers able to foster more precise medical approaches and the personalization of patient management represents an unmet clinical requirement. In this context, circulating miRNAs may represent an interesting opportunity as they can be easily detected in all biological fluids. This is particularly relevant when looking for non-invasive approaches that can be repeated over time, with no pain and stress for the oncological patient. Given that, the present review aims to describe the circulating miRNAs currently identified as associated with therapeutic treatments in OC and presents a complete overview of the available evidence.
上皮性卵巢癌(EOC)是全球最致命的癌症之一,主要原因是非特异性症状和缺乏筛查测试,这些因素共同导致诊断和治疗延迟。目前的临床生物标志物是血清CA-125,它可用于识别大多数晚期原发性和复发性疾病,并与疾病负担相关;然而,正如文献中所强调的,CA-125常常缺乏敏感性和特异性,对监测化疗反应或预测复发风险并无帮助。鉴于此,识别能够促进更精确医疗方法和患者管理个性化的新型生物标志物是一项尚未满足的临床需求。在这种背景下,循环miRNA可能是一个有趣的机会,因为它们可以在所有生物体液中轻松检测到。当寻找可以随时间重复进行、对肿瘤患者无痛苦和压力的非侵入性方法时,这一点尤为重要。鉴于此,本综述旨在描述目前确定与OC治疗相关的循环miRNA,并对现有证据进行全面概述。