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首页> 外文期刊>BMC Cancer >Differential expression of histone deacetylases HDAC1, 2 and 3 in human breast cancer - overexpression of HDAC2 and HDAC3 is associated with clinicopathological indicators of disease progression
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Differential expression of histone deacetylases HDAC1, 2 and 3 in human breast cancer - overexpression of HDAC2 and HDAC3 is associated with clinicopathological indicators of disease progression

机译:组蛋白脱乙酰基酶HDAC1、2和3在人类乳腺癌中的差异表达-HDAC2和HDAC3的过表达与疾病进展的临床病理指标有关

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Background In breast cancer, the role of epigenetic alterations including modifications of the acetylation status of histones in carcinogenesis has been an important research focus during the last years. An increased deacetylation of histones leads to increased cell proliferation, cell migration, angiogenesis and invasion. Class 1 histone deacetylases (HDAC) seem to be most important during carcinogenesis. Methods The immunhistochemical expression of HDAC1, 2 and 3 was analyzed on tissue microarrays (TMAs) from 238 patients with primary breast cancer. We analyzed the nuclear staining intensity (negative, weak, moderate, strong) as well as the percentage of positive tumor cells and calculated the immunoreactivity score (0–12). Expression was correlated with clinicopathological parameters and patient survival. Results In this cohort, we found a differential positive expression of HDAC1, HDAC2 and HDAC3. HDAC2 and HDAC3 expression was significantly higher in less differentiated tumors: HDAC2 (n=207), pConclusion As a conclusion, our results show that the class-1 HDAC isoenzymes 1, 2 and 3 are differentially expressed in breast cancer. HDAC2 and HDAC3 are strongly expressed in subgroups of tumor with features of a more aggressive tumor type.
机译:背景技术在乳腺癌中,表观遗传学改变(包括组蛋白的乙酰化状态改变在致癌作用中的作用)在最近几年一直是重要的研究重点。组蛋白脱乙酰基增加导致细胞增殖,细胞迁移,血管生成和侵袭增加。 1类组蛋白脱乙酰基酶(HDAC)在致癌过程中似乎是最重要的。方法在238例原发性乳腺癌患者的组织芯片上分析HDAC1、2和3的免疫组织化学表达。我们分析了核染色强度(阴性,弱,中,强)以及阳性肿瘤细胞的百分比,并计算了免疫反应评分(0-12)。表达与临床病理参数和患者生存率相关。结果在该队列中,我们发现了HDAC1,HDAC2和HDAC3的差异阳性表达。在分化程度较低的肿瘤中,HDAC2和HDAC3的表达明显更高:HDAC2(n = 207),p结论结论:我们的结果表明,乳腺癌中1类HDAC同工酶1、2和3差异表达。 HDAC2和HDAC3在具有较高侵袭性肿瘤类型特征的肿瘤亚组中强烈表达。

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