Center for Drug Discovery, Baylor College of Medicine, Houston, Texas, USA.
Department of Pathology & Immunology, Baylor College of Medicine, Houston, Texas, USA.
Mol Reprod Dev. 2024 Oct;91(10):e70000. doi: 10.1002/mrd.70000.
The development of novel non-hormonal male contraceptives represents a pivotal frontier in reproductive health, driven by the need for safe, effective, and reversible contraceptive methods. This comprehensive review explores the genetic underpinnings of male fertility, emphasizing the crucial roles of specific genes and structural variants (SVs) identified through advanced sequencing technologies such as long-read sequencing (LRS). LRS has revolutionized the detection of structural variants and complex genomic regions, offering unprecedented precision and resolution over traditional next-generation sequencing (NGS). Key genetic targets, including those implicated in spermatogenesis and sperm motility, are highlighted, showcasing their potential as non-hormonal contraceptive targets. The review delves into the systematic identification and validation of male reproductive tract-specific genes, utilizing advanced transcriptomics and genomics studies with validation using novel knockout mouse models. We discuss the innovative application of small molecule inhibitors, developed through platforms like DNA-encoded chemistry technology (DEC-Tec), which have shown significant promise in preclinical models. Notable examples include inhibitors targeting serine/threonine kinase 33 (STK33), soluble adenylyl cyclase (sAC), cyclin-dependent kinase 2 (CDK2), and bromodomain testis associated (BRDT), each demonstrating nanomolar affinity and potential for reversible and specific inhibition of male fertility. This review also honors the contributions of Dr. David L. Garbers whose foundational work has paved the way for these advancements. The integration of genomic, proteomic, and chemical biology approaches, supported by interdisciplinary collaboration, is poised to transform male contraceptive development. Future perspectives emphasize the need for continued innovation and rigorous testing to bring these novel contraceptives from the laboratory to clinical application, promising a new era of male reproductive health management.
新型非激素男性避孕药的开发代表了生殖健康的一个关键前沿领域,这是出于对安全、有效和可逆避孕方法的需求。本综述探讨了男性生育力的遗传基础,强调了通过长读测序(LRS)等先进测序技术鉴定的特定基因和结构变异(SVs)的关键作用。LRS 彻底改变了结构变异和复杂基因组区域的检测,提供了传统下一代测序(NGS)无法比拟的精度和分辨率。突出了包括参与精子发生和精子运动的基因在内的关键遗传靶标,展示了它们作为非激素避孕药靶标的潜力。该综述深入探讨了男性生殖道特异性基因的系统鉴定和验证,利用先进的转录组学和基因组学研究,并使用新型基因敲除小鼠模型进行验证。我们讨论了通过 DNA 编码化学技术(DEC-Tec)等平台开发的小分子抑制剂的创新应用,这些抑制剂在临床前模型中显示出了显著的前景。值得注意的例子包括靶向丝氨酸/苏氨酸激酶 33(STK33)、可溶性腺苷酸环化酶(sAC)、细胞周期蛋白依赖性激酶 2(CDK2)和溴结构域睾丸相关(BRDT)的抑制剂,每个抑制剂都具有纳摩尔亲和力和可逆且特异性抑制男性生育力的潜力。该综述还向 David L. Garbers 博士的贡献致敬,他的基础工作为这些进展铺平了道路。基因组学、蛋白质组学和化学生物学方法的整合,得到了跨学科合作的支持,有望改变男性避孕药的开发。未来的展望强调需要持续创新和严格测试,将这些新型避孕药从实验室推向临床应用,有望开创男性生殖健康管理的新时代。