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Reliable in vitro studies require appropriate ovarian cancer cell lines.可靠的体外研究需要合适的卵巢癌细胞系。
J Ovarian Res. 2014 Jun 7;7:60. doi: 10.1186/1757-2215-7-60. eCollection 2014.
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Characterization of ovarian cancer cell lines as in vivo models for preclinical studies.将卵巢癌细胞系表征为临床前研究的体内模型。
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Drug discovery using clinical outcome-based Connectivity Mapping: application to ovarian cancer.基于临床结果的连接图谱在药物发现中的应用:在卵巢癌中的应用
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Should All Cases of High-Grade Serous Ovarian, Tubal, and Primary Peritoneal Carcinomas Be Reclassified as Tubo-Ovarian Serous Carcinoma?所有高级别浆液性卵巢癌、输卵管癌和原发性腹膜癌病例都应重新分类为输卵管卵巢浆液性癌吗?
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Tubal origin of ovarian cancer - the double-edged sword of haemoglobin.卵巢癌的输卵管起源——血红蛋白的双刃剑
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Differential roles of uPAR in peritoneal ovarian carcinomatosis.uPAR 在腹膜卵巢癌转移中的差异作用。
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[Ovarian cancer--from biology to clinic].[卵巢癌——从生物学到临床]
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The organoid: A research model for ovarian cancer.类器官:一种卵巢癌研究模型。
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本文引用的文献

1
Transformation of the fallopian tube secretory epithelium leads to high-grade serous ovarian cancer in Brca;Tp53;Pten models.Brca;Tp53;Pten 模型中,输卵管分泌上皮的转化导致高级别浆液性卵巢癌。
Cancer Cell. 2013 Dec 9;24(6):751-65. doi: 10.1016/j.ccr.2013.10.013.
2
Gene expression signature of normal cell-of-origin predicts ovarian tumor outcomes.正常细胞起源的基因表达特征可预测卵巢肿瘤的预后。
PLoS One. 2013 Nov 26;8(11):e80314. doi: 10.1371/journal.pone.0080314. eCollection 2013.
3
ARID1A mutations and PI3K/AKT pathway alterations in endometriosis and endometriosis-associated ovarian carcinomas.ARID1A 突变和 PI3K/AKT 通路改变在子宫内膜异位症和子宫内膜异位症相关卵巢癌中的作用。
Int J Mol Sci. 2013 Sep 12;14(9):18824-49. doi: 10.3390/ijms140918824.
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Type-specific cell line models for type-specific ovarian cancer research.用于特定类型卵巢癌研究的特定类型细胞系模型。
PLoS One. 2013 Sep 4;8(9):e72162. doi: 10.1371/journal.pone.0072162. eCollection 2013.
5
Origin and pathogenesis of pelvic (ovarian, tubal, and primary peritoneal) serous carcinoma.盆腔(卵巢、输卵管和原发性腹膜)浆液性癌的起源和发病机制。
Annu Rev Pathol. 2014;9:27-45. doi: 10.1146/annurev-pathol-020712-163949. Epub 2013 Aug 5.
6
Evaluating cell lines as tumour models by comparison of genomic profiles.通过基因组图谱比较评估细胞系作为肿瘤模型。
Nat Commun. 2013;4:2126. doi: 10.1038/ncomms3126.
7
Early telomere shortening and genomic instability in tubo-ovarian preneoplastic lesions.卵巢小管-性腺交界性肿瘤的端粒缩短和基因组不稳定性。
Clin Cancer Res. 2013 Jun 1;19(11):2873-82. doi: 10.1158/1078-0432.CCR-12-3947. Epub 2013 Apr 15.
8
Ovarian surface epithelium as a source of ovarian cancers: unwarranted speculation or evidence-based hypothesis?卵巢表面上皮作为卵巢癌的来源:毫无根据的推测还是基于证据的假说?
Gynecol Oncol. 2013 Jul;130(1):246-51. doi: 10.1016/j.ygyno.2013.03.021. Epub 2013 Apr 2.
9
Hiding in plain view: genetic profiling reveals decades old cross contamination of bladder cancer cell line KU7 with HeLa.藏于众目睽睽之下:基因分析揭示膀胱癌细胞系 KU7 与 HeLa 之间长达数十年的交叉污染。
J Urol. 2013 Oct;190(4):1404-9. doi: 10.1016/j.juro.2013.03.009. Epub 2013 Mar 7.
10
Ovarian surface epithelium at the junction area contains a cancer-prone stem cell niche.交界区卵巢表面上皮包含一个易患癌的干细胞巢。
Nature. 2013 Mar 14;495(7440):241-5. doi: 10.1038/nature11979. Epub 2013 Mar 6.

可靠的体外研究需要合适的卵巢癌细胞系。

Reliable in vitro studies require appropriate ovarian cancer cell lines.

作者信息

Jacob Francis, Nixdorf Sheri, Hacker Neville F, Heinzelmann-Schwarz Viola A

机构信息

Ovarian Cancer Group, Adult Cancer Program, Lowy Cancer Centre, Prince of Wales Clinical School, University of New South Wales, Sydney, Australia ; Department of Biomedicine, Gynecological Research Group, University Hospital Basel, University of Basel, Basel, Switzerland.

Ovarian Cancer Group, Adult Cancer Program, Lowy Cancer Centre, Prince of Wales Clinical School, University of New South Wales, Sydney, Australia.

出版信息

J Ovarian Res. 2014 Jun 7;7:60. doi: 10.1186/1757-2215-7-60. eCollection 2014.

DOI:10.1186/1757-2215-7-60
PMID:24936210
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4058698/
Abstract

Ovarian cancer is the fifth most common cause of cancer death in women and the leading cause of death from gynaecological malignancies. Of the 75% women diagnosed with locally advanced or disseminated disease, only 30% will survive five years following treatment. This poor prognosis is due to the following reasons: limited understanding of the tumor origin, unclear initiating events and early developmental stages of ovarian cancer, lack of reliable ovarian cancer-specific biomarkers, and drug resistance in advanced cases. In the past, in vitro studies using cell line models have been an invaluable tool for basic, discovery-driven cancer research. However, numerous issues including misidentification and cross-contamination of cell lines have hindered research efforts. In this study we examined all ovarian cancer cell lines available from cell banks. Hereby, we identified inconsistencies in the reporting, difficulties in the identification of cell origin or clinical data of the donor patients, restricted ethnic and histological type representation, and a lack of tubal and peritoneal cancer cell lines. We recommend that all cell lines should be distributed via official cell banks only with strict guidelines regarding the minimal available information required to improve the quality of ovarian cancer research in future.

摘要

卵巢癌是女性癌症死亡的第五大常见原因,也是妇科恶性肿瘤死亡的主要原因。在被诊断为局部晚期或播散性疾病的女性中,只有30%的人在治疗后能存活五年。这种不良预后归因于以下原因:对肿瘤起源的了解有限、卵巢癌起始事件和早期发育阶段不明确、缺乏可靠的卵巢癌特异性生物标志物以及晚期病例中的耐药性。过去,使用细胞系模型的体外研究一直是基础的、探索性癌症研究的宝贵工具。然而,包括细胞系错误识别和交叉污染在内的诸多问题阻碍了研究工作。在本研究中,我们检查了细胞库中所有可用的卵巢癌细胞系。据此,我们发现了报告中的不一致之处、细胞起源或供体患者临床数据识别方面的困难、种族和组织学类型代表性受限以及缺乏输卵管和腹膜癌细胞系的情况。我们建议所有细胞系应仅通过官方细胞库分发,并制定严格的指导方针,规定所需的最少可用信息,以提高未来卵巢癌研究的质量。