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比较不同动物模型中卵巢早衰的动物建模和治疗方法。

Comparison of the different animal modeling and therapy methods of premature ovarian failure in animal model.

机构信息

Department of Obstetrics and Gynecology, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei, China.

Department of Obstetrics and Gynecology Ultrasound, Renmin Hospital of Wuhan University, Wuhan, 430060, China.

出版信息

Stem Cell Res Ther. 2023 May 18;14(1):135. doi: 10.1186/s13287-023-03333-4.

Abstract

Incidence of premature ovarian failure (POF) is higher with the increase of the pace of life. The etiology of POF is very complex, which is closely related to genes, immune diseases, drugs, surgery, and psychological factors. Ideal animal models and evaluation indexes are essential for drug development and mechanism research. In our review, we firstly summarize the modeling methods of different POF animal models and compare their advantages and disadvantages. Recently, stem cells are widely studied for tumor treatment and tissue repair with low immunogenicity, high homing ability, high ability to divide and self-renew. Hence, we secondly reviewed recently published data on transplantation of stem cells in the POF animal model and analyzed the possible mechanism of their function. With the further insights of immunological and gene therapy, the combination of stem cells with other therapies should be actively explored to promote the treatment of POF in the future. Our article may provide guidance and insight for POF animal model selection and new drug development.

摘要

生活节奏加快导致卵巢早衰 (POF) 的发病率增高。POF 的病因非常复杂,与基因、自身免疫性疾病、药物、手术和心理因素密切相关。理想的动物模型和评估指标对于药物开发和机制研究至关重要。在我们的综述中,我们首先总结了不同 POF 动物模型的建模方法,并比较了它们的优缺点。最近,干细胞因其低免疫原性、高归巢能力、高分裂和自我更新能力,在肿瘤治疗和组织修复方面得到了广泛研究。因此,我们其次综述了最近关于干细胞在 POF 动物模型中移植的研究数据,并分析了其功能的可能机制。随着对免疫和基因治疗的进一步深入了解,应该积极探索干细胞与其他疗法的结合,以促进未来 POF 的治疗。我们的文章可能为 POF 动物模型选择和新药开发提供指导和思路。

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Current approaches for the treatment of premature ovarian failure with stem cell therapy.干细胞治疗治疗卵巢早衰的当前方法。
Biomed Pharmacother. 2018 Jun;102:254-262. doi: 10.1016/j.biopha.2018.03.056. Epub 2018 Mar 22.

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