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印度三阴性乳腺癌女性配对血清和组织样本中特定miRNA特征的鉴定

Identification of Specific miRNA Signature in Paired Sera and Tissue Samples of Indian Women with Triple Negative Breast Cancer.

作者信息

Thakur Seema, Grover Rajesh K, Gupta Sanjay, Yadav Ajay K, Das Bhudev C

机构信息

Dr. B.R. Ambedker Centre for Biomedical Research, University of Delhi, New Delhi, India.

Delhi State Cancer Institute, Delhi, India.

出版信息

PLoS One. 2016 Jul 12;11(7):e0158946. doi: 10.1371/journal.pone.0158946. eCollection 2016.

Abstract

Of several subtypes of breast cancer, triple negative breast cancer (TNBC) is a highly aggressive tumor that lacks expression of hormone receptors for estrogen, progesterone and human epidermal growth factor receptor 2 and shows a worst prognosis. The small noncoding RNAs (miRNAs) considered as master regulator of gene expression play a key role in cancer initiation, progression and drug resistance and have emerged as attractive molecular biomarkers for diagnosis, prognosis and treatment targets in cancer. We have done expression profiling of selected miRNAs in paired serum and tissue samples of TNBC patients and corresponding cell lines and compared with that of other subtypes, in order to identify novel serum miRNA biomarkers for early detection and progression of TNBC. A total of 85 paired tumor tissues and sera with an equal number of adjacent normal tissue margins and normal sera from age matched healthy women including tissue and sera samples from 15 benign fibroadenomas were employed for the study. We report for the first time an extremely high prevalence (73.9%) of TNBC in premenopausal women below 35 years of age and a significant altered expression of a panel of three specific oncogenic miRNAs- miR-21, miR-221, miR-210, and three tumor suppressor miRNAs- miR-195, miR-145 and Let-7a in both tissues and corresponding sera of TNBC patients when compared with triple positive breast cancer (TPBC) patients. While miR-21, miR-221 and miR-210 showed significant over-expression, miR-195 and miR-145 were downregulated and well correlated with various clinicopathological and demographic risk factors, tumor grade, clinical stage and hormone receptor status. Interestingly, despite being a known tumor suppressor, Let-7a showed a significant overexpression in TNBCs. It is suggested that this panel of six miRNA signature may serve as a minimally invasive biomarker for an early detection of TNBC patients.

摘要

在几种乳腺癌亚型中,三阴性乳腺癌(TNBC)是一种侵袭性很强的肿瘤,它缺乏雌激素、孕激素和人表皮生长因子受体2的激素受体表达,预后最差。被认为是基因表达主要调节因子的小非编码RNA(miRNA)在癌症的发生、发展和耐药性中起关键作用,并已成为癌症诊断、预后和治疗靶点的有吸引力的分子生物标志物。我们对TNBC患者的配对血清和组织样本以及相应细胞系中的选定miRNA进行了表达谱分析,并与其他亚型进行了比较,以确定用于TNBC早期检测和进展的新型血清miRNA生物标志物。本研究共使用了85对肿瘤组织和血清,以及来自年龄匹配的健康女性的数量相等的相邻正常组织边缘和正常血清,其中包括15个良性纤维腺瘤的组织和血清样本。我们首次报告,在35岁以下的绝经前女性中,TNBC的患病率极高(73.9%),并且与三阳性乳腺癌(TPBC)患者相比,TNBC患者的组织和相应血清中一组三种特定致癌miRNA——miR-21、miR-221、miR-210,以及三种肿瘤抑制miRNA——miR-195、miR-145和Let-7a的表达有显著改变。虽然miR-21、miR-221和miR-210显示出显著的过表达,但miR-195和miR-145被下调,且与各种临床病理和人口统计学风险因素、肿瘤分级、临床分期和激素受体状态密切相关。有趣的是,尽管Let-7a是一种已知的肿瘤抑制因子,但它在TNBC中显示出显著的过表达。建议这六种miRNA特征组合可作为TNBC患者早期检测的微创生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09ba/4942139/105a04d0bfba/pone.0158946.g001.jpg

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