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PDE5 抑制剂及 NO/cGMP 通路在癌症中的作用。

The Role of PDE5 Inhibitors and the NO/cGMP Pathway in Cancer.

机构信息

Department of Urology, Tulane University Health Sciences Center, New Orleans, LA, USA.

Department of Pharmacology, School of Pharmacy, Ankara University, Ankara, Turkey.

出版信息

Sex Med Rev. 2016 Jan;4(1):74-84. doi: 10.1016/j.sxmr.2015.10.004. Epub 2016 Jan 8.

Abstract

INTRODUCTION

Phosphodiesterase 5 (PDE5) inhibitors (PDE5i) have been used clinically for the treatment of erectile dysfunction, acting on the nitric oxide/cyclic guanosine monophosphate (NO/cGMP) signaling pathway. Simultaneously, researchers have elucidated the roles that this pathway plays in the regulation of cell proliferation, tumor development, and progression. As a result, our knowledge of PDE5i and cancer biology has expanded and provides an integration that holds great promise for some, but concern for others.

AIM

This review evaluates the role of PDE5i and the NO/cGMP signaling pathway in the pathogenesis and prevention of various malignancies.

METHODS

A literature review was performed with regard to the role of NO/cGMP pathway in tumor formation and prevention in preclinical and clinical studies. Studies that utilized PDE5i to further explore the involvement of this pathway also were included.

MAIN OUTCOME MEASURES

To evaluate whether PDE5i provide a potential benefit for treating and/or preventing malignancies; or if they create potential harm leading to the development of these malignancies.

RESULTS

The best available data suggest that the interactions between PDE5i and cancer are tumor- and tissue-specific. Currently, the effect of PDE5i use on melanoma development is being debated. Further clinical controversy lies in PDE5i use for penile rehabilitation after nerve-sparing prostate cancer surgery. Preclinical studies suggest that PDE5 inhibition could lead to a decreased risk of developing colorectal and breast cancer, leukemia, and myeloma. PDE5i also may provide an additional antitumor immune response. Finally, researchers have demonstrated a synergistic effect from combining PDE5i with current chemotherapeutic regimens.

CONCLUSION

Currently, there are inadequate data to make any conclusive statements regarding the role of PDE5i in cancer pathogenesis and how to alter clinical management. In order to create appropriate clinical guidelines, further experimental and clinical evidence is required.

摘要

简介

磷酸二酯酶 5(PDE5)抑制剂(PDE5i)已在临床上用于治疗勃起功能障碍,作用于一氧化氮/环鸟苷酸(NO/cGMP)信号通路。同时,研究人员阐明了该通路在细胞增殖、肿瘤发生和进展中的作用。因此,我们对 PDE5i 和癌症生物学的认识不断扩大,并为一些人提供了很大的希望,但也引起了其他人的担忧。

目的

本综述评估了 PDE5i 和 NO/cGMP 信号通路在各种恶性肿瘤发病机制和预防中的作用。

方法

对 NO/cGMP 通路在临床前和临床研究中肿瘤形成和预防中的作用进行文献复习。还包括利用 PDE5i 进一步探讨该通路参与的研究。

主要观察指标

评估 PDE5i 是否为治疗和/或预防恶性肿瘤提供潜在益处;或者它们是否会造成潜在危害,导致这些恶性肿瘤的发生。

结果

目前最好的数据表明,PDE5i 与癌症之间的相互作用具有肿瘤和组织特异性。目前,关于 PDE5i 对黑色素瘤发展的影响存在争议。进一步的临床争议在于 PDE5i 在前列腺癌神经保留手术后阴茎康复中的应用。临床前研究表明,PDE5 抑制可能会降低结直肠癌、乳腺癌、白血病和骨髓瘤的发病风险。PDE5i 还可能提供额外的抗肿瘤免疫反应。最后,研究人员还证明了 PDE5i 与当前化疗方案联合使用具有协同作用。

结论

目前,关于 PDE5i 在癌症发病机制中的作用以及如何改变临床管理,还没有足够的数据得出任何结论性的陈述。为了制定适当的临床指南,需要进一步的实验和临床证据。

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