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慢速冷冻保存通过体内和体外方法确保了高卵巢组织质量,并且对生育力保存是安全的。

Slow-Freezing Cryopreservation Ensures High Ovarian Tissue Quality Followed by In Vivo and In Vitro Methods and Is Safe for Fertility Preservation.

作者信息

Gudlevičienė Živilė, Žilinskas Kastytis, Kundrotas Gabrielis, Grubliauskaitė Monika, Baltriukienė Daiva, Bukelskienė Virginija

机构信息

Department of Biobank, National Cancer Institute, Santariskiu Str. 1, 08660 Vilnius, Lithuania.

Department of Oncogynecology, National Cancer Institute, Santariskiu Str. 1, 08660 Vilnius, Lithuania.

出版信息

Medicina (Kaunas). 2020 Oct 19;56(10):547. doi: 10.3390/medicina56100547.

DOI:10.3390/medicina56100547
PMID:33086522
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7603126/
Abstract

Cancer incidence is growing with younger patients diagnosed with this disease every year. Improved cancer diagnostics and treatment lead to better survival of cancer patients. However, after aggressive chemo- or radiotherapy, cancer survivors suffer from various degrees of subfertility or infertility. Several fertility preservation technologies have been developed for young cancer patients: cryopreservation of germ cells, embryos, or reproductive tissues. The best results have been shown by cryopreservation of sperm and embryos. Yet the success of using cryopreserved oocytes or reproductive tissues (ovarian and testicular) is still insufficient. Therefore, this study was designed to assess the vitality, viability, general quality, and safety of frozen-thawed human ovarian tissue for retransplantation using modern molecular tests. The new miRNA array test was used to evaluate miRNA expression in thawed ovarian tissue in combination with standard xenotransplantation and pathological examination of microslides. Our results demonstrated that slow freezing is an efficient way (80%) to cryopreserve ovarian tissue with no structural damage afterwards. We have shown that xenotransplantation into immunodeficient mice, histology, and immunohistochemistry could be potentially replaced by more recent molecular methods. The latter method has shown that altered expression of miRNAs might be used as identifiers of normal/damaged tissue after further analysis. Newer, safer, and more specific approaches need to be developed in order to eliminate the risk of disease reoccurrence.

摘要

癌症发病率逐年上升,每年都有更年轻的患者被诊断出患有这种疾病。癌症诊断和治疗的改善使癌症患者的生存率提高。然而,在积极的化疗或放疗后,癌症幸存者会遭受不同程度的生育力下降或不育。针对年轻癌症患者已经开发了几种生育力保存技术:生殖细胞、胚胎或生殖组织的冷冻保存。精子和胚胎的冷冻保存显示出了最好的效果。然而,使用冷冻保存的卵母细胞或生殖组织(卵巢和睾丸)的成功率仍然不足。因此,本研究旨在使用现代分子检测方法评估冻融后人卵巢组织再移植的活力、生存能力、总体质量和安全性。新的miRNA阵列检测被用于结合标准异种移植和显微切片的病理检查来评估解冻后卵巢组织中的miRNA表达。我们的结果表明,慢速冷冻是一种有效的(80%)卵巢组织冷冻保存方法,之后不会造成结构损伤。我们已经表明,将其移植到免疫缺陷小鼠体内、组织学和免疫组织化学检测可能会被更新的分子方法所取代。后一种方法表明,miRNA表达的改变在进一步分析后可能用作正常/受损组织的标识符。需要开发更新、更安全、更特异的方法,以消除疾病复发的风险。

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本文引用的文献

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Overexpression of circulating MiR-30b-5p identifies advanced breast cancer.循环 miR-30b-5p 的过表达可识别晚期乳腺癌。
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miRDB: an online database for prediction of functional microRNA targets.miRDB:一个用于预测功能 microRNA 靶标的在线数据库。
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Immature Oocyte for Fertility Preservation.用于生育力保存的未成熟卵母细胞。
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Comparison between Slow Freezing and Vitrification for Human Ovarian Tissue Cryopreservation and Xenotransplantation.慢速冻与玻璃化法在人卵巢组织冻存及异种移植中的比较。
Int J Mol Sci. 2019 Jul 8;20(13):3346. doi: 10.3390/ijms20133346.
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Initial steps in reconstruction of the human ovary: survival of pre-antral stage follicles in a decellularized human ovarian scaffold.人类卵巢重建的初始步骤:去细胞化人卵巢支架中原始卵泡的存活。
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Sci Rep. 2019 Jul 3;9(1):9636. doi: 10.1038/s41598-019-45642-w.
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