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hnRNP A/B 蛋白在人非小细胞肺癌中的失调表达:配对肿瘤/非肿瘤组织中蛋白和 mRNA 水平的平行评估。

Deregulated expression of hnRNP A/B proteins in human non-small cell lung cancer: parallel assessment of protein and mRNA levels in paired tumour/non-tumour tissues.

机构信息

RNA Processing Program, Institute of Biological Research and Biotechnology, National Hellenic Research Foundation, 48 Vas Constantinou Avenue, 11635 Athens, Greece.

出版信息

BMC Cancer. 2010 Aug 17;10:434. doi: 10.1186/1471-2407-10-434.

Abstract

BACKGROUND

Heterogeneous nuclear ribonucleoproteins (hnRNPs) of the A/B type (hnRNP A1, A2/B1, A3) are highly related multifunctional proteins participating in alternative splicing by antagonising other splicing factors, notably ASF/SF2. The altered expression pattern of hnRNP A2/B1 and/or splicing variant B1 alone in human lung cancer and their potential to serve as molecular markers for early diagnosis remain issues of intense investigation. The main objective of the present study was to use paired tumour/non-tumour biopsies from patients with non-small cell lung cancer (NSCLC) to investigate the expression profiles of hnRNP A1, A2/B1 and A3 in conjunction with ASF/SF2.

METHODS

We combined western blotting of tissue homogenates with immunohistochemical examination of fixed tissue sections and quantification of mRNA expression levels in tumour versus adjacent normal-looking areas of the lung in the same patient.

RESULTS

Our study, in addition to clear evidence of mostly uncoupled deregulation of hnRNPs A/B, has revealed hnRNP A1 to be the most deregulated protein with a high frequency of over-expression (76%), followed by A3 (52%) and A2/B1 (43%). Moreover, direct comparison of protein/mRNA levels showed a lack of correlation in the case of hnRNP A1 (as well as of ASF/SF2), but not of A2/B1, suggesting that different mechanisms underlie their deregulation.

CONCLUSION

Our results provide strong evidence for the up-regulation of hnRNP A/B in NSCLC, and they support the existence of distinct mechanisms responsible for their deregulated expression.

摘要

背景

异质核核糖核蛋白(hnRNP)A/B 型(hnRNP A1、A2/B1、A3)是高度相关的多功能蛋白,通过拮抗其他剪接因子(尤其是 ASF/SF2)参与可变剪接。hnRNP A2/B1 和/或剪接变体 B1 在人类肺癌中的表达模式改变及其作为早期诊断的分子标志物的潜力仍然是深入研究的问题。本研究的主要目的是使用非小细胞肺癌(NSCLC)患者的配对肿瘤/非肿瘤活检,结合 ASF/SF2 研究 hnRNP A1、A2/B1 和 A3 的表达谱。

方法

我们将组织匀浆的 Western 印迹与固定组织切片的免疫组织化学检查以及同一患者肿瘤与相邻正常肺区域的 mRNA 表达水平定量相结合。

结果

除了 hnRNP A/B 失调的明显证据外,我们的研究还揭示了 hnRNP A1 是失调最严重的蛋白,其高表达频率为 76%,其次是 A3(52%)和 A2/B1(43%)。此外,蛋白质/mRNA 水平的直接比较表明,hnRNP A1(以及 ASF/SF2)缺乏相关性,但 A2/B1 则没有,这表明它们的失调有不同的机制。

结论

我们的结果为 NSCLC 中 hnRNP A/B 的上调提供了有力证据,并支持存在不同的机制导致它们的失调表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5fa/2933625/20f8c4d886a7/1471-2407-10-434-1.jpg

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