Current and Future Directions of Stem Cell Therapy for Bladder Dysfunction

Author:

Shin Jung Hyun,Ryu Chae-Min,Yu Hwan Yeul,Shin Dong-Myung,Choo Myung-SooORCID

Abstract

AbstractStem cells are capable of self-renewal and differentiation into a range of cell types and promote the release of chemokines and progenitor cells necessary for tissue regeneration. Mesenchymal stem cells are multipotent progenitor cells with enhanced proliferation and differentiation capabilities and less tumorigenicity than conventional adult stem cells; these cells are also easier to acquire. Bladder dysfunction is often chronic in nature with limited treatment modalities due to its undetermined pathophysiology. Most treatments focus on symptom alleviation rather than pathognomonic changes repair. The potential of stem cell therapy for bladder dysfunction has been reported in preclinical models for stress urinary incontinence, overactive bladder, detrusor underactivity, and interstitial cystitis/bladder pain syndrome. Despite these findings, however, stem cell therapy is not yet available for clinical use. Only one pilot study on detrusor underactivity and a handful of clinical trials on stress urinary incontinence have reported the effects of stem cell treatment. This limitation may be due to stem cell function loss following ex vivo expansion, poor in vivo engraftment or survival after transplantation, or a lack of understanding of the precise mechanisms of action underlying therapeutic outcomes and in vivo behavior of stem cells administered to target organs. Efficacy comparisons with existing treatment modalities are also needed for the successful clinical application of stem cell therapies. This review describes the current status of stem cell research on treating bladder dysfunction and suggests future directions to facilitate clinical applications of this promising treatment modality, particularly for bladder dysfunction.

Publisher

Springer Science and Business Media LLC

Reference89 articles.

1. Ratajczak, M. Z., Ratajczak, J., Suszynska, M., Miller, D. M., Kucia, M., & Shin, D. M. (2017). A novel view of the adult stem cell compartment from the perspective of a quiescent population of very small embryonic-like stem cells. Circulation Research, 120(1), 166–178.

2. Heo, J., Lim, J., Lee, S., Jeong, J., Kang, H., Kim, Y., Kang, J. W., Yu, H. Y., Jeong, E. M., Kim, K., Kucia, M., Waigel, S. J., Zacharias, W., Chen, Y., Kim, I. G., Ratajczak, M. Z., & Shin, D. M. (2017). Sirt1 regulates DNA methylation and differentiation potential of embryonic stem cells by antagonizing Dnmt3l. Cell Reports, 18(8), 1930–1945.

3. Jeong, H., Yim, H. W., Park, H. J., Cho, Y., Hong, H., Kim, N. J., & Oh, I. H. (2018). Mesenchymal stem cell therapy for ischemic heart disease: Systematic review and meta-analysis. International Journal of Stem Cells, 11(1), 1–12.

4. Kim, Y., Jin, H. J., Heo, J., Ju, H., Lee, H. Y., Kim, S., Lee, S., Lim, J., Jeong, S. Y., Kwon, J., Kim, M., Choi, S. J., Oh, W., Yang, Y. S., Hwang, H. H., Yu, H. Y., Ryu, C. M., Jeon, H. B., & Shin, D. M. (2018). Small hypoxia-primed mesenchymal stem cells attenuate graft-versus-host disease. Leukemia, 32(12), 2672–2684.

5. Jeong, E. M., Yoon, J. H., Lim, J., Shin, J. W., Cho, A. Y., Heo, J., Lee, K. B., Lee, J. H., Lee, W. J., Kim, H. J., Son, Y. H., Lee, S. J., Cho, S. Y., Shin, D. M., Choi, K., & Kim, I. G. (2018). Real-time monitoring of glutathione in living cells reveals that high glutathione levels are required to maintain stem cell function. Stem Cell Reports, 10(2), 600–614.

Cited by 25 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3