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离子通道的表达和功能在实体瘤和血管畸形中会发生显著改变。

Ion channels expression and function are strongly modified in solid tumors and vascular malformations.

作者信息

Biasiotta Antonella, D'Arcangelo Daniela, Passarelli Francesca, Nicodemi Ezio Maria, Facchiano Antonio

机构信息

Department of Neurology and Psychiatry, Sapienza University, Rome, Italy.

Istituto Dermopatico dell'Immacolata, IDI-IRCCS, Fondazione Luigi Maria Monti, via Monti di Creta 104, 00167, Rome, Italy.

出版信息

J Transl Med. 2016 Oct 4;14(1):285. doi: 10.1186/s12967-016-1038-y.

Abstract

BACKGROUND

Several cellular functions relate to ion-channels activity. Physiologically relevant chains of events leading to angiogenesis, cell cycle and different forms of cell death, require transmembrane voltage control. We hypothesized that the unordered angiogenesis occurring in solid cancers and vascular malformations might associate, at least in part, to ion-transport alteration.

METHODS

The expression level of several ion-channels was analyzed in human solid tumor biopsies. Expression of 90 genes coding for ion-channels related proteins was investigated within the Oncomine database, in 25 independent patients-datasets referring to five histologically-different solid tumors (namely, bladder cancer, glioblastoma, melanoma, breast invasive-ductal cancer, lung carcinoma), in a total of 3673 patients (674 control-samples and 2999 cancer-samples). Furthermore, the ion-channel activity was directly assessed by measuring in vivo the electrical sympathetic skin responses (SSR) on the skin of 14 patients affected by the flat port-wine stains vascular malformation, i.e., a non-tumor vascular malformation clinical model.

RESULTS

Several ion-channels showed significantly increased expression in tumors (p < 0.0005); nine genes (namely, CACNA1D, FXYD3, FXYD5, HTR3A, KCNE3, KCNE4, KCNN4, CLIC1, TRPM3) showed such significant modification in at least half of datasets investigated for each cancer type. Moreover, in vivo analyses in flat port-wine stains patients showed a significantly reduced SSR in the affected skin as compared to the contralateral healthy skin (p < 0.05), in both latency and amplitude measurements.

CONCLUSIONS

All together these data identify ion-channel genes showing significantly modified expression in different tumors and cancer-vessels, and indicate a relevant electrophysiological alteration in human vascular malformations. Such data suggest a possible role and a potential diagnostic application of the ion-electron transport in vascular disorders underlying tumor neo-angiogenesis and vascular malformations.

摘要

背景

多种细胞功能与离子通道活性相关。导致血管生成、细胞周期及不同形式细胞死亡的生理相关事件链需要跨膜电压控制。我们推测实体癌和血管畸形中发生的无序血管生成可能至少部分与离子转运改变有关。

方法

分析了人类实体瘤活检组织中几种离子通道的表达水平。在Oncomine数据库中,研究了25个独立患者数据集(涉及5种组织学不同的实体瘤,即膀胱癌、胶质母细胞瘤、黑色素瘤、乳腺浸润性导管癌、肺癌)中90个编码离子通道相关蛋白的基因的表达情况,共计3673例患者(674例对照样本和2999例癌症样本)。此外,通过在14例患有扁平葡萄酒色斑血管畸形(一种非肿瘤性血管畸形临床模型)的患者皮肤上测量体内电交感皮肤反应(SSR),直接评估离子通道活性。

结果

几种离子通道在肿瘤中表达显著增加(p < 0.0005);9个基因(即CACNA1D、FXYD3、FXYD5、HTR3A、KCNE3、KCNE4、KCNN4、CLIC1、TRPM3)在每种癌症类型研究的至少一半数据集中显示出这种显著变化。此外,对扁平葡萄酒色斑患者的体内分析显示,与对侧健康皮肤相比,患侧皮肤的SSR在潜伏期和波幅测量中均显著降低(p < 0.05)。

结论

所有这些数据确定了在不同肿瘤和癌血管中表达显著改变的离子通道基因,并表明人类血管畸形存在相关的电生理改变。这些数据提示离子 - 电子转运在肿瘤新生血管形成和血管畸形相关的血管疾病中可能具有作用及潜在的诊断应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38f5/5050926/563e8d3b932e/12967_2016_1038_Fig1_HTML.jpg

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