School of Pharmaceutical Sciences & Yunnan Provincial Key Laboratory of Pharmacology for Natural Products, Kunming Medical University, 1168 West Chun Rong Road, Cheng Gong, Kunming, Yunnan, 650500, People's Republic of China.
Department of Gynecologic Oncology, The Third Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, People's Republic of China.
J Ovarian Res. 2017 Nov 13;10(1):75. doi: 10.1186/s13048-017-0369-5.
Limited understanding of ovarian cancer (OC) genome portrait has hindered the therapeutic advances. The serial monitoring of tumor genotypes is becoming increasingly attainable with circulating cell-free DNA (cf-DNA) and circulating tumor cells (CTCs) emerging as "liquid biopsies". They represent non-invasive biomarkers and are viable, as they can be isolated from human plasma, serum and other body fluids. Molecular characterization of circulating tumor DNA (ct-DNA) and CTCs offer unique potentials to better understand the biology of metastasis and resistance to therapies. The liquid biopsies may also give innovative insights into the process of rapid and accurate identification, resistant genetic alterations and a real time monitoring of treatment responses. In addition, liquid biopsies are shedding light on elucidating signal pathways involved in invasiveness and metastasis competence; but the detection and molecular characterization of ct-DNA and CTCs are still challenging, since they are rare, and the amount of available samples are very limited. This review will focus on the clinical potential of ct-DNA and CTCs in both the early and advanced diagnosis, prognosis, and in the identification of resistance mutations in OC.
对卵巢癌 (OC) 基因组图谱的有限了解阻碍了治疗的进展。随着循环游离 DNA (cf-DNA) 和循环肿瘤细胞 (CTC) 的出现,肿瘤基因型的连续监测变得越来越可行,它们作为“液体活检”成为可能。它们代表了非侵入性生物标志物,并且是可行的,因为它们可以从人体血浆、血清和其他体液中分离出来。循环肿瘤 DNA (ct-DNA) 和 CTCs 的分子特征为更好地了解转移和对治疗的耐药性生物学提供了独特的潜力。液体活检也可能为快速准确地识别、耐药遗传改变和实时监测治疗反应提供创新的见解。此外,液体活检还阐明了参与侵袭性和转移能力的信号通路;但 ct-DNA 和 CTCs 的检测和分子特征仍然具有挑战性,因为它们数量很少,可用样本量非常有限。这篇综述将重点介绍 ct-DNA 和 CTCs 在 OC 的早期和晚期诊断、预后以及耐药突变识别中的临床潜力。