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首页> 外文期刊>Breast cancer research and treatment. >Prognostic value of tumor cell DNA content determined by flow cytometry using formalin-fixed paraffin-embedded breast cancer tissues
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Prognostic value of tumor cell DNA content determined by flow cytometry using formalin-fixed paraffin-embedded breast cancer tissues

机译:流式细胞仪使用福尔马林固定的石蜡包埋乳腺癌组织测定肿瘤细胞DNA含量的预后值

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PurposeThe use of formalin-fixed paraffin-embedded (FFPE) tumor tissues in flow cytometry (FCM)-based determination of tumor cell DNA content is more complicated than the use of fresh-frozen tissues. This study aimed to accurately measure tumor cell DNA content from FFPE tissues by separating tumor cells from stromal cells through FCM and investigating its prognostic impact.MethodsWe separately measured the DNA contents of tumor cells and stromal cells by gating with pan-cytokeratin and vimentin (FCMC/V). We evaluated tumor cell DNA contents [DNA index (DI)] of 290 FFPE tumor tissues and classified them into low and high DI groups, using a cutoff DI value determined through an unbiased computational method.ResultsThe distribution of DI was bimodal, and a cutoff value was determined at a DI of 1.26. The high-DI tumors were associated with aggressive phenotypes and had significantly worse distant recurrence-free intervals (DRFI) than low-DI tumors. Multivariate analysis revealed that lymph node metastasis, Ki67, and DI were independent factors affecting DRFI. Accordingly, patients with low-DI/low-Ki67 tumors had excellent outcomes compared with other tumor types. Multiploid tumors were associated with increased lymphocytic infiltration and aggressive phenotypes.ConclusionsThe DI of FFPE tumors could be precisely determined through FCMC/V. A combination of DI and Ki67 analyses may be able to predict the prognoses of breast cancer patients with greater accuracy.
机译:用福尔马林固定的石蜡包埋(FFPE)肿瘤组织在流式细胞术(FCM)中的使用比使用新鲜冷冻组织的使用更加复杂。本研究旨在通过将肿瘤细胞从基质细胞分离通过FCM来精确测量来自FFPE组织的肿瘤细胞DNA含量,并研究其预后抗冲击。近奇地用PAN-Cytokeratin和Vimentin(FCMC)分别测量肿瘤细胞和基质细胞的DNA含量和基质细胞的DNA含量(FCMC / v)。我们评估了290个FFPE肿瘤组织的肿瘤细胞DNA含量[DNA指数(DI)]并将它们分为低和高DI族,使用通过无偏的计算方法确定的切断DI值。DI的分布是双峰,以及截止值在1.26的DI中确定。高DI肿瘤与腐蚀性表型相关,并且具有比低DI肿瘤的远程复发间隔(DRFI)显着差。多变量分析显示,淋巴结转移,KI67和DI是影响DRFI的独立因素。因此,与其他肿瘤类型相比,低DI /低ki67肿瘤的患者具有出色的结果。多倍曲线肿瘤与增加的淋巴细胞浸润和腐蚀性表型相关。可以通过FCMC / v精确地确定FFPE肿瘤的组合。 DI和KI67分析的组合可能能够更高准确地预测乳腺癌患者的预期。

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