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光化性角化病中异常基因表达的微阵列分析:Toll样受体7激动剂咪喹莫特的作用

Microarray analysis of aberrant gene expression in actinic keratosis: effect of the Toll-like receptor-7 agonist imiquimod.

作者信息

Torres A, Storey L, Anders M, Miller R L, Bulbulian B J, Jin J, Raghavan S, Lee J, Slade H B, Birmachu W

机构信息

Dermatology Office, Loma Linda University Medical Center, Loma Linda, CA, USA.

出版信息

Br J Dermatol. 2007 Dec;157(6):1132-47. doi: 10.1111/j.1365-2133.2007.08218.x. Epub 2007 Oct 18.

Abstract

BACKGROUND

The molecular events leading to actinic keratosis (AK) are not well understood.

OBJECTIVE

To identify and compare gene expression changes in AK lesions and in sun-exposed nonlesional skin and to determine the effect of imiquimod 5% cream on these changes.

METHOD

A double-blind, vehicle-controlled, randomized study was conducted to evaluate the molecular changes in AK treated with imiquimod. Seventeen male subjects with >/= 5 AK lesions on the scalp applied vehicle or imiquimod three times a week for 4 weeks. Gene expression analysis using Affymetrix oligonucleotide arrays was performed on shave biopsies of lesions taken before and after treatment. Confocal microscopy was performed on the study area as an adjunctive diagnostic procedure.

RESULTS

We identified gene expression changes which occur in sun-exposed, nonlesional skin as well as in AK lesions. These changes include, but are not limited to, the overexpression of oncogenic and proliferative genes and diminished expression of tumour suppressor genes. The gene expression changes observed in AK lesions and in sun-exposed, nonlesional skin were consistent with the confocal microscopy observations, which showed abnormalities in the sun-exposed, nonlesional skin, similar in nature but less pronounced than abnormalities seen in AK. Imiquimod partially or totally reversed the aberrant expression of some of the genes observed in AK, consistent with clearing of lesions and normalization of confocal cellular images.

CONCLUSIONS

The data show that profound gene expression changes occur in sun-exposed, nonlesional skin which progress further in AK lesions. The data also suggest that imiquimod may play a role in normalizing gene expression and cellular morphology in sun-damaged skin.

摘要

背景

导致光化性角化病(AK)的分子事件尚未完全明确。

目的

识别并比较AK皮损与阳光暴露的非皮损皮肤中的基因表达变化,并确定5%咪喹莫特乳膏对这些变化的影响。

方法

开展一项双盲、赋形剂对照、随机研究,以评估咪喹莫特治疗AK的分子变化。17名头皮上有≥5个AK皮损的男性受试者,每周3次外用赋形剂或咪喹莫特,共4周。使用Affymetrix寡核苷酸阵列对治疗前后病变的剃刀活检组织进行基因表达分析。在研究区域进行共聚焦显微镜检查作为辅助诊断程序。

结果

我们识别出在阳光暴露的非皮损皮肤以及AK皮损中发生的基因表达变化。这些变化包括但不限于致癌和增殖基因的过表达以及肿瘤抑制基因表达的减少。在AK皮损和阳光暴露的非皮损皮肤中观察到的基因表达变化与共聚焦显微镜观察结果一致,共聚焦显微镜观察显示阳光暴露的非皮损皮肤存在异常,其性质与AK中所见异常相似,但程度较轻。咪喹莫特部分或完全逆转了AK中观察到的一些基因的异常表达,这与皮损消退和共聚焦细胞图像正常化一致。

结论

数据表明,在阳光暴露的非皮损皮肤中发生了深刻的基因表达变化,这些变化在AK皮损中进一步发展。数据还表明,咪喹莫特可能在使光损伤皮肤中的基因表达和细胞形态正常化方面发挥作用。

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