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佩罗尼氏病:治疗靶点的研究进展。

Peyronie's disease: perspectives on therapeutic targets.

机构信息

Division of Andrology, Mansoura , Egypt.

出版信息

Expert Opin Ther Targets. 2011 Aug;15(8):913-29. doi: 10.1517/14728222.2011.577419. Epub 2011 Apr 14.

DOI:10.1517/14728222.2011.577419
PMID:21492024
Abstract

INTRODUCTION

Peyronie's disease (PD) is an acquired benign connective tissue disorder of the penis, characterized by the development of fibrotic plaques, that can cause different degrees of bending, narrowing or shortening. Medical treatment for PD remains a major challenge. Impressive progress in our understanding of the molecular mechanisms of PD pathogenesis has uncovered several promising molecular targets for antifibrotic treatments.

AREAS COVERED

This review covers the literature pertaining to the exploration of therapeutic targets for PD. The search included: i) a MEDLINE search from 1941 to January 2011, limited to English-language medical literature, ii) relevant abstracts from 2009 and 2010, iii) relevant textbooks and iv) a pipeline search for therapeutics in development.

EXPERT OPINION

Rapid translational research depends on our ability to develop rational therapies targeted to penile tunical fibrosis, which necessitate a sound knowledge of the biology, biochemistry and the physiological role of fibroblasts, myofibroblasts and stem cells in PD. Much remains to be learned about the pathogenesis of PD. Although there are many interesting therapeutic targets, we are confronted with some questions when identifying new targets, or when validating potential therapeutic options.

摘要

简介

佩罗尼氏病(PD)是一种获得性阴茎良性结缔组织疾病,其特征为纤维斑块的形成,可导致不同程度的弯曲、变窄或缩短。PD 的医学治疗仍然是一个主要挑战。对 PD 发病机制的分子机制的理解取得了令人瞩目的进展,为抗纤维化治疗揭示了几个有前途的分子靶点。

涵盖领域

这篇综述涵盖了 PD 治疗靶点探索的文献。搜索包括:i)从 1941 年到 2011 年 1 月的 MEDLINE 搜索,仅限于英文医学文献,ii)2009 年和 2010 年的相关摘要,iii)相关教科书和 iv)正在开发的治疗药物的流水线搜索。

专家意见

快速转化研究取决于我们开发针对阴茎白膜纤维化的合理疗法的能力,这需要对纤维化、肌成纤维细胞和干细胞在 PD 中的生物学、生物化学和生理作用有一个正确的认识。PD 的发病机制仍有许多需要了解的地方。虽然有许多有趣的治疗靶点,但在确定新靶点或验证潜在的治疗选择时,我们面临着一些问题。

相似文献

1
Peyronie's disease: perspectives on therapeutic targets.佩罗尼氏病:治疗靶点的研究进展。
Expert Opin Ther Targets. 2011 Aug;15(8):913-29. doi: 10.1517/14728222.2011.577419. Epub 2011 Apr 14.
2
Experimental models of Peyronie's disease. Implications for new therapies.佩罗尼氏病的实验模型。对新疗法的启示。
J Sex Med. 2009 Feb;6(2):303-13. doi: 10.1111/j.1743-6109.2008.01104.x. Epub 2008 Dec 2.
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BJU Int. 2012 Jul;110(1):117-21. doi: 10.1111/j.1464-410X.2011.10733.x. Epub 2011 Dec 16.
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Pathophysiology and Future Therapeutic Perspectives for Resolving Fibrosis in Peyronie's Disease.探讨阴茎硬结症纤维化治疗的病理生理学和未来治疗前景
Sex Med Rev. 2019 Oct;7(4):679-689. doi: 10.1016/j.sxmr.2019.02.004. Epub 2019 Apr 5.
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Mechanisms of Disease: new insights into the cellular and molecular pathology of Peyronie's disease.疾病机制:佩罗尼氏病细胞与分子病理学的新见解
Nat Clin Pract Urol. 2005 Jun;2(6):291-7. doi: 10.1038/ncpuro0201.
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Basic fibroblast growth factor expression in Peyronie's disease.佩罗尼氏病中碱性成纤维细胞生长因子的表达
J Urol. 2001 Feb;165(2):419-23. doi: 10.1097/00005392-200102000-00016.
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Antifibrotic Synergy Between Phosphodiesterase Type 5 Inhibitors and Selective Oestrogen Receptor Modulators in Peyronie's Disease Models.在佩罗尼病模型中,磷酸二酯酶 5 抑制剂与选择性雌激素受体调节剂的抗纤维化协同作用。
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Radiation increases fibrogenic cytokine expression by Peyronie's disease fibroblasts.辐射会增加佩罗尼氏病成纤维细胞的促纤维化细胞因子表达。
J Urol. 2003 Jul;170(1):281-4. doi: 10.1097/01.ju.0000070860.78370.08.
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Pharmacologic therapy for Peyronie's disease: what should we prescribe?佩罗尼氏病的药物治疗:我们应该开什么药?
Expert Opin Pharmacother. 2015 Jun;16(9):1299-311. doi: 10.1517/14656566.2015.1041503. Epub 2015 Apr 30.
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Implications of nitric oxide synthase isoforms in the pathophysiology of Peyronie's disease.一氧化氮合酶同工型在佩罗尼氏病病理生理学中的意义。
Int J Impot Res. 2002 Oct;14(5):345-52. doi: 10.1038/sj.ijir.3900872.

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Int J Impot Res. 2020 May;32(3):281-288. doi: 10.1038/s41443-019-0136-9. Epub 2019 Apr 15.
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Peyronie's Disease Treated with Oral Weekly Dexamethasone and Continuous Low-dose Cyclophosphamide.口服每周一次地塞米松和持续低剂量环磷酰胺治疗佩罗尼氏病
Indian J Dermatol. 2014 May;59(3):317. doi: 10.4103/0019-5154.131463.