卵巢癌建模的新面貌:更好的检测和治疗前景。

F1000 medicine reports Pub Date : 2011-01-01 Epub Date: 2011-11-01 DOI:10.3410/M3-22
Alison M Karst, Ronny Drapkin
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引用次数: 21

摘要

卵巢癌具有不成比例的高死亡率,因为患者通常表现为晚期转移性疾病。这些死亡绝大多数来自高级别浆液性癌。最近的研究表明,许多此类肿瘤起源于输卵管,随后转移到卵巢。这也许可以解释为什么这些肿瘤没有在早期被发现,因为检测的努力仅仅集中在卵巢上。随着对离体模型的发展和人类输卵管上皮细胞的永生化等其他进展的理解的飞跃,以及使用综合基因组分析来鉴定数百种可能参与肿瘤发生的新的候选癌基因和肿瘤抑制因子,现在我们可以开始真正定义输卵管和卵巢源性肿瘤之间发病机制的差异。这样做,我们有望改善早期发现、治疗和结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The new face of ovarian cancer modeling: better prospects for detection and treatment.

The new face of ovarian cancer modeling: better prospects for detection and treatment.

The new face of ovarian cancer modeling: better prospects for detection and treatment.

The new face of ovarian cancer modeling: better prospects for detection and treatment.

Ovarian cancer has a disproportionately high mortality rate because patients typically present with late-stage metastatic disease. The vast majority of these deaths are from high-grade serous carcinoma. Recent studies indicate that many of these tumors arise from the fallopian tube and subsequently metastasize to the ovary. This may explain why such tumors have not been detected at early stage as detection efforts have been focused purely on the ovary. In keeping with this leap in understanding other advances such as the development of ex-vivo models and immortalization of human fallopian tube epithelial cells, and the use of integrated genomic analyses to identify hundreds of novel candidate oncogenes and tumor suppressors potentially involved in tumorigenesis now engender hope that we can begin to truly define the differences in pathogenesis between fallopian tube and ovarian-derived tumors. In doing so, we can hopefully improve early detection, treatment, and outcome.

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