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本文引用的文献

1
Status of tumor markers in ovarian cancer screening.肿瘤标志物在卵巢癌筛查中的现状。
J Clin Oncol. 2003 May 15;21(10 Suppl):200s-205s. doi: 10.1200/JCO.2003.01.068.
2
Activation and overexpression of centrosome kinase BTAK/Aurora-A in human ovarian cancer.中心体激酶BTAK/Aurora-A在人类卵巢癌中的激活与过表达。
Clin Cancer Res. 2003 Apr;9(4):1420-6.
3
Female mice chimeric for expression of the simian virus 40 TAg under control of the MISIIR promoter develop epithelial ovarian cancer.在MISIIR启动子控制下嵌合表达猿猴病毒40 TAg的雌性小鼠会发生上皮性卵巢癌。
Cancer Res. 2003 Mar 15;63(6):1389-97.
4
Loss of cellular retinol-binding protein 1 gene expression in microdissected human ovarian cancer.显微切割的人类卵巢癌中细胞视黄醇结合蛋白1基因表达缺失
Clin Cancer Res. 2003 Mar;9(3):1013-20.
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Specific keynote: chemoprevention of ovarian cancer: the journey begins.专题主旨:卵巢癌的化学预防:征程伊始。
Gynecol Oncol. 2003 Jan;88(1 Pt 2):S59-66; discussion S67-70. doi: 10.1006/gyno.2002.6686.
6
LOT1 (PLAGL1/ZAC1), the candidate tumor suppressor gene at chromosome 6q24-25, is epigenetically regulated in cancer.位于6号染色体q24 - 25区域的候选抑癌基因LOT1(PLAGL1/ZAC1)在癌症中受到表观遗传调控。
J Biol Chem. 2003 Feb 21;278(8):6041-9. doi: 10.1074/jbc.M210361200. Epub 2002 Dec 6.
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Early events in ovarian epithelial carcinogenesis: progress and problems in experimental approaches.卵巢上皮癌发生的早期事件:实验方法的进展与问题
Int J Gynecol Cancer. 2002 Nov-Dec;12(6):691-703. doi: 10.1046/j.1525-1438.2002.01152.x.
8
Dynamic alterations of the extracellular environment of ovarian surface epithelial cells in premalignant transformation, tumorigenicity, and metastasis.卵巢表面上皮细胞在癌前转化、致瘤性和转移过程中细胞外环境的动态变化。
Cancer. 2002 Oct 15;95(8):1802-15. doi: 10.1002/cncr.10870.
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BRCA1 methylation: a significant role in tumour development?BRCA1甲基化:在肿瘤发展中起重要作用?
Semin Cancer Biol. 2002 Oct;12(5):359-371. doi: 10.1016/s1044-579x(02)00056-1.
10
Development of a highly specialized cDNA array for the study and diagnosis of epithelial ovarian cancer.用于上皮性卵巢癌研究与诊断的高度专业化cDNA芯片的研发。
Cancer Res. 2002 May 15;62(10):2923-8.

卵巢肿瘤发生的早期事件。

Early events in ovarian oncogenesis.

作者信息

Cvetkovic Dusica

机构信息

Ovarian Cancer Program, Division of Medical Science, Fox Chase Cancer Center, Philadelphia, PA, USA.

出版信息

Reprod Biol Endocrinol. 2003 Oct 7;1:68. doi: 10.1186/1477-7827-1-68.

DOI:10.1186/1477-7827-1-68
PMID:14577833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC239895/
Abstract

Ovarian cancer represents the most lethal of the gynecological neoplasms. The molecular and genetic events associated with early ovarian oncogenesis are still largely unknown, thus contributing to the lack of reliable biomarkers for disease detection. Since the majority of ovarian tumors are diagnosed at an advanced stage, the availability of early ovarian cancer tissue samples for molecular analyses is very limited. In this review, problems encountered in the study of early ovarian cancer are presented, along with the controversies concerning precursor lesions and stepwise progression towards ovarian malignancy. Experimental modeling in the development of ovarian cancer is also described, as well as genetic and epigenetic alterations associated with early ovarian cancer. Lastly, examples of technological advances in the study of early ovarian cancer are discussed. Hopefully, the increasing knowledge about molecular and genetic events involved in the early stages of ovarian tumorigenesis will provide the basis for management of ovarian cancer in the future.

摘要

卵巢癌是最致命的妇科肿瘤。与早期卵巢肿瘤发生相关的分子和遗传事件在很大程度上仍不清楚,这导致缺乏用于疾病检测的可靠生物标志物。由于大多数卵巢肿瘤在晚期才被诊断出来,用于分子分析的早期卵巢癌组织样本非常有限。在这篇综述中,介绍了早期卵巢癌研究中遇到的问题,以及关于前驱病变和向卵巢恶性肿瘤逐步发展的争议。还描述了卵巢癌发展过程中的实验模型,以及与早期卵巢癌相关的遗传和表观遗传改变。最后,讨论了早期卵巢癌研究中的技术进步实例。希望对卵巢肿瘤发生早期所涉及的分子和遗传事件的不断了解,将为未来卵巢癌的管理提供依据。