miR-3648介导的APC2 1失调参与早期发病和乳腺癌进展

M. Batool, J. Qadir, Misbah Shan, Feiya Li, F. A. Malik, H. M. Awan
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引用次数: 0

摘要

多种癌症的发生是由于Wnt信号通路的畸变。几种mirna调节无翼集成(Wnt)信号通路的组成部分。miR-3648是一种人类特异性mirna,由于其最小的脱靶效应而引起特别关注。在本研究中,我们研究了miR-3648和APC2在巴基斯坦乳腺癌患者中的表达。采用实时荧光定量PCR方法观察组织样本中miR-3648和APC2表达与临床病理特征及乳腺癌亚型的相关性。我们的研究结果显示,miR-3648在Luminal A亚型中相对下调,APC2在这些患者中相应上调。此外,在发病早、绝经前、肿瘤分级低、临床分期早、无淋巴结侵袭和转移的乳腺癌女性中,miR-3648和APC2的转录水平均被发现呈负调控,进一步提示了这些分子在乳腺癌发生和进展中的分子相互作用。
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Involvement of miR-3648 mediated APC2 1 dysregulation in early onset and breast cancer progression
Multiple cancers arise due to aberrations in the Wnt signaling pathway. Several miRNAs modulate the integral components of the wingless integrated (Wnt) signaling pathway. miR-3648 is a human-specific miRNAs that is of particular interest due to its minimal off-targeting effect. In this study, we investigated the expression of miR-3648 and APC2 in breast cancer patients of Pakistan. Correlations of miR-3648 and APC2 expression with clinico-pathological features and breast cancer subtypes were observed in tissue samples by means of quantitative real time PCR. Our results showed that miR-3648 was relatively downregulated in Luminal A subtype, with corresponding upregulation of APC2 in these patients. Moreover, the transcript levels of both miR-3648 and APC2 were found to be inversely regulated in breast cancer women presented with early disease onset, pre-menopause, low tumor grade, early clinical stage, absence of nodal invasion and metastasis, further suggesting the molecular interplay of these molecules in breast cancer development and progression.
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来源期刊
Kuwait Journal of Science & Engineering
Kuwait Journal of Science & Engineering MULTIDISCIPLINARY SCIENCES-
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3 months
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