therapeutic development

治疗发展
  • 文章类型: Journal Article
    这篇综述纪念发现用于间变性淋巴瘤激酶(ALK)和白细胞酪氨酸激酶(LTK)的生理配体Augmentorα(Augmentorα;ALKAL2;Fam150b)和Augmentorβ(Augmentorβ;ALKAL1;Fam150a)的10周年,以前被认为是孤儿受体。本文对ALK家族受体的生物物理和细胞特性及其在癌症中的作用进行了深入的综述。新陈代谢,疼痛,眼科,色素沉着,中枢神经系统(CNS)功能,和繁殖。ALK和LTK受体与许多癌症的发展有关。和靶向抑制它们的信号通路可以提供治疗益处。此外,ALK家族受体参与调节体重和代谢,调节疼痛信号,有助于眼睛发育和色素沉着。在中枢神经系统,这些受体在突触调节中起作用,神经发生,和各种精神病。最后,ALK的表达与生殖功能有关,对接受ALK抑制剂治疗的患者有潜在影响。需要进一步的研究来更好地了解ALK家族受体和Aug配体的复杂相互作用,并重新调整靶向治疗广泛的人类疾病。
    This review commemorates the 10-year anniversary of the discovery of physiological ligands Augα (Augmentor α; ALKAL2; Fam150b) and Augβ (Augmentor β; ALKAL1; Fam150a) for anaplastic lymphoma kinase (ALK) and leukocyte tyrosine kinase (LTK), previously considered orphan receptors. This manuscript provides an in-depth review of the biophysical and cellular properties of ALK family receptors and their roles in cancer, metabolism, pain, ophthalmology, pigmentation, central nervous system (CNS) function, and reproduction. ALK and LTK receptors are implicated in the development of numerous cancers, and targeted inhibition of their signaling pathways can offer therapeutic benefits. Additionally, ALK family receptors are involved in regulating body weight and metabolism, modulating pain signaling, and contributing to eye development and pigmentation. In the CNS, these receptors play a role in synapse modulation, neurogenesis, and various psychiatric pathologies. Lastly, ALK expression is linked to reproductive functions, with potential implications for patients undergoing ALK inhibitor therapy. Further research is needed to better understand the complex interactions of ALK family receptors and Aug ligands and to repurpose targeted therapy for a wide range of human diseases.
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  • 文章类型: Journal Article
    这篇综述深入研究了神经免疫学,重点关注其与多发性硬化症(MS)的相关性和潜在的治疗进展。神经免疫学探索免疫系统和中枢神经系统(CNS)之间的复杂关系。了解这些机制对于掌握MS等疾病的病理生理学和设计创新治疗方法至关重要。这篇综述介绍了基础神经免疫学概念,强调免疫细胞的作用,细胞因子,和中枢神经系统稳定性中的血脑屏障。它强调了它们的失调如何导致MS,并讨论了影响MS易感性的遗传和环境因素。前沿研究方法,从组学技术到先进的成像,彻底改变了我们对MS的理解,提供有价值的诊断和预后工具。这篇评论还涉及到有趣的肠-脑轴,研究肠道微生物群如何影响神经免疫过程及其潜在的治疗意义。目前的MS治疗,从免疫调节药物到疾病改善疗法,与有前途的实验方法一起讨论。个性化医疗的潜力,基于细胞的治疗,并探讨了基因治疗在MS管理中的应用。总之,这篇综述强调了神经免疫学在MS研究中的意义,这表明,更深入的了解可以为MS和类似病症的更量身定制和有效的治疗铺平道路。神经免疫学的持续研究和合作对于提高患者预后至关重要。
    This review delves into neuroimmunology, focusing on its relevance to multiple sclerosis (MS) and potential treatment advancements. Neuroimmunology explores the intricate relationship between the immune system and the central nervous system (CNS). Understanding these mechanisms is vital for grasping the pathophysiology of diseases like MS and for devising innovative treatments. This review introduces foundational neuroimmunology concepts, emphasizing the role of immune cells, cytokines, and blood-brain barrier in CNS stability. It highlights how their dysregulation can contribute to MS and discusses genetic and environmental factors influencing MS susceptibility. Cutting-edge research methods, from omics techniques to advanced imaging, have revolutionized our understanding of MS, offering valuable diagnostic and prognostic tools. This review also touches on the intriguing gut-brain axis, examining how gut microbiota impacts neuroimmunological processes and its potential therapeutic implications. Current MS treatments, from immunomodulatory drugs to disease-modifying therapies, are discussed alongside promising experimental approaches. The potential of personalized medicine, cell-based treatments, and gene therapy in MS management is also explored. In conclusion, this review underscores neuroimmunology\'s significance in MS research, suggesting that a deeper understanding could pave the way for more tailored and effective treatments for MS and similar conditions. Continued research and collaboration in neuroimmunology are essential for enhancing patient outcomes.
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  • 文章类型: Journal Article
    UNASSIGNED: The Institute of Translational Health Sciences (ITHS), a Clinical and Translational Science Award (CTSA)-funded program at the University of Washington (UW), established the Drug and Device Advisory Committee (DDAC) to provide product-specific scientific and regulatory mentoring to investigators seeking to translate their discoveries into medical products. An 8-year retrospective analysis was undertaken to evaluate the impact of the DDAC programs on commercialization metrics.
    UNASSIGNED: Tracked metrics included the number of teams who consulted with the DDAC, initiated a clinical trial, formed a startup, or were successful obtaining federal small business innovation awards or venture capital. The review includes historical comparisons of the startup rates for the UW School of Medicine and the Fred Hutchinson Cancer Research Center, two ITHS-affiliated institutions that have had different DDAC utilization rates.
    UNASSIGNED: Between 2008 and 2016, the DDAC supported 161 unique project teams, 28% of which went on to form a startup. The commercialization rates for the UW School of Medicine increased significantly following integration of the DDAC into the commercialization programs offered by the UW technology transfer office.
    UNASSIGNED: A formalized partnership between preclinical consulting and the technology transfer programs provides an efficient use of limited development funds and a more in-depth vetting of the business opportunity and regulatory path to development.
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