前列腺健康的新治疗前沿:与BPH和前列腺癌比较的新分子靶点和经典途径。

Muhammad Sajjad Hassan, Hafiz Muhammad Irfan, Alamgeer, Muavia Sarwar, Zeeshan Jabbar, Shoaib Nawaz
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引用次数: 0

摘要

目前良性前列腺增生(BPH)和前列腺癌的治疗策略主要集中在雄激素受体(AR)和5- α还原酶抑制,以抑制雄激素驱动的前列腺生长。然而,这些方法往往会导致副作用和耐药性。最近的研究发现了新的靶点,如整合素和钙粘蛋白抑制剂、基因调控、microrna、细胞衰老和代谢组学途径,以克服这些局限性。与传统的雄激素治疗相比,这些创新提供了更个性化的治疗方法,潜在的副作用更少,耐药性也更低。新的靶点和通路,无论是抑制的还是过表达的,都为前列腺疾病的信号调节提供了控制点,这表明通过创新外源性物质治疗的未来潜力。数据来自谷歌Scholar、PubMed和谷歌,以突出这些新兴方法在提高前列腺健康治疗效果方面的比较潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emerging therapeutic frontiers in prostate health: Novel molecular targets and classical pathways in comparison with BPH and prostate cancer.

Current therapeutic strategies for benign prostatic hyperplasia (BPH) and prostate cancer focus mainly on androgen receptors (AR) and 5-alpha reductase inhibition to suppress androgen-driven prostate growth. However, these methods often result in side effects and resistance. Recent research identifies novel targets like integrin and cadherin inhibitors, gene regulation, microRNAs, cellular senescence, and metabolomics pathways to overcome these limitations. These innovations offer more personalized approaches with potentially fewer adverse effects and reduced resistance compared to traditional androgen-focused therapies. Novel target sites and pathways, either suppressed or overexpressed, offer control points for modulating signaling in prostate diseases, suggesting future potential for treatment through innovative exogenous substances. Data was compiled from Google Scholar, PubMed, and Google to highlight the comparative potential of these emerging methods in enhancing treatment efficacy for prostate health.

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