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可变聚腺苷酸化与非小细胞肺癌中PABPN1的低表达及不良预后相关。

Alternative polyadenylation is associated with lower expression of PABPN1 and poor prognosis in non-small cell lung cancer.

作者信息

Ichinose Junji, Watanabe Kousuke, Sano Atsushi, Nagase Takahide, Nakajima Jun, Fukayama Masashi, Yatomi Yutaka, Ohishi Nobuya, Takai Daiya

机构信息

Department of Thoracic Surgery, University of Tokyo Hospital, Tokyo, Japan.

出版信息

Cancer Sci. 2014 Sep;105(9):1135-41. doi: 10.1111/cas.12472. Epub 2014 Sep 3.

Abstract

Alternative polyadenylation (APA), which induces shortening of the 3'UTR, is emerging as an important phenomenon in gene regulation. APA is involved in development, cancer and cell proliferation. APA may lead to disruption of microRNA-mediated gene silencing in cancer cells via detachment of microRNA binding sites. We studied the correlation between the APA profile and the tumor aggressiveness in cases of lung cancer. We selected the top 10 genes showing significant 3'UTR shortening in lung cancer, using the package of the Bioconductor for probe-level analyses of expression microarrays. We established and evaluated the APA score by quantitative RT-PCR in 147 clinical specimens of non-small cell lung cancer and compared the results with the clinical outcomes and expression levels of APA-related genes, including PABPN1, CPEB1, E2F1 and proliferation markers (MKI67, TOP2A and MCM2). High APA scores were correlated with an advanced tumor stage and a poor prognosis (P < 0.001). Multivariate analysis identified the APA score as an independent prognostic factor (hazard ratio, 3.0; P = 0.03). Both lower expression of PABPN1 and higher expression of the proliferation markers were correlated with high APA scores and a poor prognosis, with suppression of PABPN1 exerting its influence independent of gain of the proliferation markers. Moreover, the APA score was correlated with the maximum standardized uptake value of the tumors on positron emission tomography (r = 0.53; P < 0.001). Our results indicate that the loss of PABPN1, a suppressor of APA, might promote tumor aggressiveness by releasing the cancer cells from microRNA-mediated gene regulation.

摘要

可变聚腺苷酸化(APA)可导致3'非翻译区(3'UTR)缩短,正逐渐成为基因调控中的一种重要现象。APA参与发育、癌症和细胞增殖过程。在癌细胞中,APA可能通过使微小RNA结合位点脱离而导致微小RNA介导的基因沉默被破坏。我们研究了肺癌病例中APA谱与肿瘤侵袭性之间的相关性。我们使用生物导体软件包对表达微阵列进行探针水平分析,筛选出肺癌中显示3'UTR显著缩短的前10个基因。我们通过定量逆转录聚合酶链反应(RT-PCR)在147例非小细胞肺癌临床标本中建立并评估了APA评分,并将结果与临床结局以及APA相关基因(包括PABPN1、CPEB1、E2F1)和增殖标志物(MKI67、TOP2A和MCM2)的表达水平进行比较。高APA评分与肿瘤晚期和预后不良相关(P < 0.001)。多变量分析确定APA评分为独立的预后因素(风险比,3.0;P = 0.03)。PABPN1表达降低和增殖标志物表达升高均与高APA评分和预后不良相关,PABPN1的抑制作用独立于增殖标志物的增加发挥作用。此外,APA评分与正电子发射断层扫描中肿瘤的最大标准化摄取值相关(r = 0.53;P < 0.001)。我们的结果表明,作为APA抑制剂的PABPN1缺失可能通过使癌细胞从微小RNA介导的基因调控中释放出来,从而促进肿瘤侵袭性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58a7/4462401/9e87b52d21d7/cas0105-1135-f1.jpg

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