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过氧化物酶体增殖物激活受体 γ,蕈样肉芽肿的可能罪魁祸首:免疫组化研究。

Peroxisome proliferator-activated receptor gamma, a possible culprit in mycosis fungoides: an immunohistochemical study.

机构信息

Department of Dermatology, Kasr AlAini Hospital, Cairo University, Cairo, Egypt.

出版信息

J Eur Acad Dermatol Venereol. 2012 Dec;26(12):1522-32. doi: 10.1111/j.1468-3083.2011.04333.x. Epub 2011 Nov 24.

DOI:10.1111/j.1468-3083.2011.04333.x
PMID:22112149
Abstract

BACKGROUND

It still remains debatable whether peroxisome proliferator-activated receptor gamma (PPARγ) is pro- or antineoplastic, and its exact role in mycosis fungoides (MF) remains unclear.

OBJECTIVE

This prospective comparative study aimed to investigate the expression of PPARγ in MF and compare it with psoriatics and controls in a trial to deduce its possible role in MF. Also, we tried to clarify the relation between PPARγ and Bcl-2 in MF.

METHODS

Twenty MF patients, 20 psoriatic patients and 20 controls were included. All participants underwent a skin biopsy, and immunohistochemical staining for both PPARγ and Bcl-2 were performed. Western blot analysis was performed for detection of both PPARγ and Bcl-2.

RESULTS

The mean area per cent of PPARγ measured in the MF patients (57.1217±9.502417) was significantly higher (P<0.001) when compared with that of both the psoriatics (2.989±1.723) and controls (35.9357±8.1789). The mean area per cent of Bcl-2 in MF patients (9.3763±6.6328) was significantly higher (P<0.001) than that of both the psoriatics (2.35±1.35) and the controls (0.73105±0.5302)]. Our results were confirmed using the western blot analysis. We detected a highly significant positive correlation between the PPARγ and Bcl-2 mean area per cents in all patients. In our MF patients, both parameters were also positively correlated with the age of the patient, duration and stage of MF (P<0.05).

CONCLUSION

Our data suggest a possible role for PPARγ in the pathogenesis of MF possibly through several mechanisms, one of which might be conferring upon the lymphoma cells, a survival advantage at least partially through up regulating Bcl-2.

摘要

背景

过氧化物酶体增殖物激活受体 γ(PPARγ)是促进还是抑制肿瘤的作用仍存在争议,其在蕈样肉芽肿(MF)中的确切作用尚不清楚。

目的

本前瞻性对照研究旨在探讨 MF 中 PPARγ的表达,并与银屑病患者和对照组进行比较,以推断其在 MF 中的可能作用。此外,我们还试图阐明 MF 中 PPARγ与 Bcl-2 之间的关系。

方法

纳入 20 例 MF 患者、20 例银屑病患者和 20 例对照组。所有参与者均接受皮肤活检,并进行 PPARγ和 Bcl-2 的免疫组织化学染色。进行 Western blot 分析以检测 PPARγ和 Bcl-2。

结果

MF 患者的 PPARγ测量的平均面积百分比(57.1217±9.502417)明显高于银屑病患者(2.989±1.723)和对照组(35.9357±8.1789)(P<0.001)。MF 患者的 Bcl-2 平均面积百分比(9.3763±6.6328)明显高于银屑病患者(2.35±1.35)和对照组(0.73105±0.5302)(P<0.001)。Western blot 分析结果也证实了这一点。我们在所有患者中检测到 PPARγ和 Bcl-2 的平均面积百分比之间存在高度显著的正相关。在我们的 MF 患者中,这两个参数也与患者的年龄、MF 的持续时间和阶段呈正相关(P<0.05)。

结论

我们的数据表明,PPARγ 可能通过几种机制在 MF 的发病机制中发挥作用,其中一种机制可能通过上调 Bcl-2 至少部分地赋予淋巴瘤细胞生存优势。

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