首页> 美国卫生研究院文献>PLoS Clinical Trials >Defining the Sister Rat Mammary Tumor Cell Lines HH-16 cl.2/1 and HH-16.cl.4 as an In Vitro Cell Model for Erbb2
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Defining the Sister Rat Mammary Tumor Cell Lines HH-16 cl.2/1 and HH-16.cl.4 as an In Vitro Cell Model for Erbb2

机译:将姊妹大鼠乳腺肿瘤细胞系HH-16 cl.2 / 1和HH-16.cl.4定义为Erbb2的体外细胞模型

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摘要

Cancer cell lines have been shown to be reliable tools in genetic studies of breast cancer, and the characterization of these lines indicates that they are good models for studying the biological mechanisms underlying this disease. Here, we describe the molecular cytogenetic/genetic characterization of two sister rat mammary tumor cell lines, HH-16 cl.2/1 and HH-16.cl.4, for the first time. Molecular cytogenetic analysis using rat and mouse chromosome paint probes and BAC/PAC clones allowed the characterization of clonal chromosome rearrangements; moreover, this strategy assisted in revealing detected breakpoint regions and complex chromosome rearrangements. This comprehensive cytogenetic analysis revealed an increase in the number of copies of the Mycn and Erbb2 genes in the investigated cell lines. To analyze its possible correlation with expression changes, relative RNA expression was assessed by real-time reverse transcription quantitative PCR and RNA FISH. Erbb2 was found to be overexpressed in HH-16.cl.4, but not in the sister cell line HH-16 cl.2/1, even though these lines share the same initial genetic environment. Moreover, the relative expression of Erbb2 decreased after global genome demethylation in the HH-16.cl.4 cell line. As these cell lines are commercially available and have been used in previous studies, the present detailed characterization improves their value as an in vitro cell model. We believe that the development of appropriate in vitro cell models for breast cancer is of crucial importance for revealing the genetic and cellular pathways underlying this neoplasy and for employing them as experimental tools to assist in the generation of new biotherapies.
机译:癌细胞系已被证明是乳腺癌基因研究中的可靠工具,这些系的表征表明它们是研究该疾病潜在生物学机制的良好模型。在这里,我们第一次描述了两个姐妹大鼠乳腺肿瘤细胞系HH-16 cl.2 / 1和HH-16.cl.4的分子细胞遗传学/遗传学表征。使用大鼠和小鼠染色体油漆探针和BAC / PAC克隆进行分子细胞遗传学分析,可以表征克隆染色体重排;此外,该策略有助于揭示检测到的断点区域和复杂的染色体重排。这项全面的细胞遗传学分析表明,在所研究的细胞系中,Mycn和Erbb2基因的拷贝数增加了。为了分析其与表达变化的可能相关性,通过实时逆转录定量PCR和RNA FISH评估相对RNA表达。发现Erbb2在HH-16.cl.4中过表达,但在姊妹细胞系HH-16 cl.2 / 1中没有过表达,即使这些系具有相同的初始遗传环境。此外,在HH-16.cl.4细胞系中全局基因组去甲基化后,Erbb2的相对表达降低。由于这些细胞系是可商购的并且已经用于先前的研究中,因此本发明的详细表征提高了它们作为体外细胞模型的价值。我们认为,开发合适的乳腺癌体外细胞模型对于揭示这种瘤形成的遗传和细胞途径以及将其用作辅助新生物疗法产生的实验工具至关重要。

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