• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[肾上腺疾病的基因与细胞治疗:成就与展望]

[Gene and cell therapy of adrenal pathology: achievements and prospects].

作者信息

Glazova O V, Vorontsova M V, Sakr N, Shevkova L V, Onyanov N A, Kaziakhmedova S A, Volchkov P Y

机构信息

Endocrinology Research Centre; Moscow Institute of Physics and Technology (National Research University).

Moscow Institute of Physics and Technology (National Research University).

出版信息

Probl Endokrinol (Mosk). 2021 Dec 2;67(6):80-89. doi: 10.14341/probl12818.

DOI:10.14341/probl12818
PMID:35018764
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9753849/
Abstract

Our current understanding of the molecular and cellular mechanisms in tissues and organs during normal and pathological conditions opens up substantial prospects for the development of novel approaches to treatment of various diseases. For instance, lifelong replacement therapy is no longer mandatory for the management of some monogenic hereditary diseases. Genome editing techniques that have emerged in the last decade are being actively investigated as tools for correcting mutations in affected organs. Furthermore, new protocols for obtaining various types of human and animal cells and cellular systems are evolving, increasingly reflecting the real structures in vivo. These methods, together with the accompanying gene and cell therapy, are being actively developed and several approaches are already undergoing clinical trials. Adrenal insufficiency caused by a variety of factors can potentially be the target of such therapeutic strategies. The adrenal gland is a highly organized organ, with multiple structural components interacting with each other via a complex network of endocrine and paracrine signals. This review summarizes the findings of studies in the field of structural organization and functioning of the adrenal gland at the molecular level, as well as the modern approaches to the treatment of adrenal pathologies.

摘要

我们目前对组织和器官在正常及病理状态下分子和细胞机制的理解,为开发各种疾病的新型治疗方法开辟了广阔前景。例如,终身替代疗法不再是治疗某些单基因遗传病的必要手段。过去十年中出现的基因组编辑技术正在作为纠正受影响器官中突变的工具而被积极研究。此外,获取各种类型的人类和动物细胞及细胞系统的新方案不断发展,越来越多地反映体内的真实结构。这些方法连同伴随的基因和细胞疗法正在积极开发,并且有几种方法已经在进行临床试验。由多种因素引起的肾上腺功能不全可能成为此类治疗策略的目标。肾上腺是一个高度有组织的器官,其多个结构成分通过复杂的内分泌和旁分泌信号网络相互作用。本综述总结了肾上腺在分子水平上的结构组织和功能领域的研究结果,以及肾上腺疾病的现代治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a23/9753849/d402a3d46bc8/problendo-67-12818-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a23/9753849/d402a3d46bc8/problendo-67-12818-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a23/9753849/d402a3d46bc8/problendo-67-12818-g001.jpg

相似文献

1
[Gene and cell therapy of adrenal pathology: achievements and prospects].[肾上腺疾病的基因与细胞治疗:成就与展望]
Probl Endokrinol (Mosk). 2021 Dec 2;67(6):80-89. doi: 10.14341/probl12818.
2
Therapeutic editing of hepatocyte genome in vivo.体内肝细胞基因组的治疗性编辑。
J Hepatol. 2017 Oct;67(4):818-828. doi: 10.1016/j.jhep.2017.05.012. Epub 2017 May 17.
3
Towards novel treatments for adrenal diseases: Cell- and gene therapy-based approaches.针对肾上腺疾病的新型治疗方法:基于细胞和基因治疗的方法。
Mol Cell Endocrinol. 2021 Mar 15;524:111160. doi: 10.1016/j.mce.2021.111160. Epub 2021 Jan 14.
4
[Adrenal glands stem cells: general signaling pathways].[肾上腺干细胞:一般信号通路]
Probl Endokrinol (Mosk). 2021 Dec 14;67(6):90-97. doi: 10.14341/probl12819.
5
Gene Therapy with CRISPR/Cas9 Coming to Age for HIV Cure.基因治疗与 CRISPR/Cas9 渐趋成熟,有望攻克 HIV。
AIDS Rev. 2017 Oct-Dec;19(3):167-172.
6
Genome Editing of Monogenic Neuromuscular Diseases: A Systematic Review.单基因神经肌肉疾病的基因组编辑:系统评价。
JAMA Neurol. 2016 Nov 1;73(11):1349-1355. doi: 10.1001/jamaneurol.2016.3388.
7
Animal models of endocrine/organ-specific autoimmune diseases: do they really help us to understand human autoimmunity?内分泌/器官特异性自身免疫性疾病的动物模型:它们真的有助于我们理解人类自身免疫吗?
Springer Semin Immunopathol. 2002 Dec;24(3):297-321. doi: 10.1007/s00281-002-0110-2.
8
Macromolecular crowding: chemistry and physics meet biology (Ascona, Switzerland, 10-14 June 2012).大分子拥挤现象:化学与物理邂逅生物学(瑞士阿斯科纳,2012年6月10日至14日)
Phys Biol. 2013 Aug;10(4):040301. doi: 10.1088/1478-3975/10/4/040301. Epub 2013 Aug 2.
9
CRISPR-Cas9: a promising tool for gene editing on induced pluripotent stem cells.CRISPR-Cas9:一种用于诱导多能干细胞基因编辑的有前景的工具。
Korean J Intern Med. 2017 Jan;32(1):42-61. doi: 10.3904/kjim.2016.198. Epub 2017 Jan 1.
10
New aspects of endocrine control of atrial fibrillation and possibilities for clinical translation.心房颤动内分泌调控的新方面及其临床转化的可能性。
Cardiovasc Res. 2021 Jun 16;117(7):1645-1661. doi: 10.1093/cvr/cvab080.

引用本文的文献

1
Non-classical animal models for studying adrenal diseases: advantages, limitations, and implications for research.用于研究肾上腺疾病的非经典动物模型:优势、局限性及对研究的启示
Lab Anim Res. 2024 Jun 19;40(1):25. doi: 10.1186/s42826-024-00212-8.

本文引用的文献

1
Current progress in stem cell therapy for type 1 diabetes mellitus.1 型糖尿病干细胞治疗的研究进展。
Stem Cell Res Ther. 2020 Jul 8;11(1):275. doi: 10.1186/s13287-020-01793-6.
2
Extension of Survival in Bilaterally Adrenalectomized Mice by Implantation of SF-1/Ad4BP-Induced Steroidogenic Cells.通过植入SF-1/Ad4BP诱导的类固醇生成细胞延长双侧肾上腺切除小鼠的生存期
Endocrinology. 2020 Mar 1;161(3). doi: 10.1210/endocr/bqaa007.
3
Stem Cells, Self-Renewal, and Lineage Commitment in the Endocrine System.内分泌系统中的干细胞、自我更新与谱系定向分化
Front Endocrinol (Lausanne). 2019 Nov 8;10:772. doi: 10.3389/fendo.2019.00772. eCollection 2019.
4
Primary adrenal insufficiency: New genetic causes and their long-term consequences.原发性肾上腺皮质功能不全:新的遗传病因及其长期后果。
Clin Endocrinol (Oxf). 2020 Jan;92(1):11-20. doi: 10.1111/cen.14109. Epub 2019 Oct 30.
5
Disease modelling in human organoids.人类类器官中的疾病建模。
Dis Model Mech. 2019 Jul 29;12(7):dmm039347. doi: 10.1242/dmm.039347.
6
Isolated glucocorticoid deficiency: Genetic causes and animal models.孤立性糖皮质激素缺乏症:遗传病因与动物模型。
J Steroid Biochem Mol Biol. 2019 May;189:73-80. doi: 10.1016/j.jsbmb.2019.02.012. Epub 2019 Feb 25.
7
Paving the way for successful islet encapsulation.为胰岛成功封装铺平道路。
Drug Discov Today. 2019 Mar;24(3):737-748. doi: 10.1016/j.drudis.2019.01.020. Epub 2019 Feb 6.
8
Isolation and characterization of adrenocortical progenitors involved in the adaptation to stress.应激适应相关的肾上腺皮质祖细胞的分离和鉴定。
Proc Natl Acad Sci U S A. 2018 Dec 18;115(51):12997-13002. doi: 10.1073/pnas.1814072115. Epub 2018 Dec 4.
9
Human fetal adrenal cells retain age-related stem- and endocrine-differentiation potential in culture.人胎儿肾上腺细胞在培养中保留与年龄相关的干细胞和内分泌分化潜能。
FASEB J. 2019 Feb;33(2):2263-2277. doi: 10.1096/fj.201801028RR. Epub 2018 Sep 24.
10
Modeling Congenital Adrenal Hyperplasia and Testing Interventions for Adrenal Insufficiency Using Donor-Specific Reprogrammed Cells.使用供体特异性重编程细胞对先天性肾上腺增生症进行建模和测试肾上腺功能减退症的干预措施。
Cell Rep. 2018 Jan 30;22(5):1236-1249. doi: 10.1016/j.celrep.2018.01.003.