Can we really protect the ovary from chemotherapy damage?

被引:0
|
作者
Nguyen, Thuy Truong An [1 ]
Condorelli, Margherita [2 ]
Demeestere, Isabelle [1 ,2 ]
机构
[1] Univ Libre Bruxelles ULB, Fac Med, Res Lab Human Reprod, B-1070 Brussels, Belgium
[2] HUB Erasme, Fertil Clin, Dept Obstet & Gynecol, Brussels, Belgium
关键词
Chemotherapy; Ovary; Fertility preservation; Pharmacoprotection; COLONY-STIMULATING FACTOR; ABL TYROSINE KINASE; CYCLOPHOSPHAMIDE METABOLITES; INDUCED APOPTOSIS; FEMALE FERTILITY; CANCER SURVIVAL; FOLLICULAR LOSS; SPHINGOSINE-1-PHOSPHATE; CISPLATIN; ACTIVATION;
D O I
10.1016/j.bpobgyn.2025.102603
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Future alternatives to current fertility preservation methods such as pharmacological strategies to prevent chemotherapy-induced ovarian damage in female cancer patients are of growing interest. Chemotherapeutic agents, especially alkylating agents, cause DNA damage and apoptosis in ovarian follicles, significantly reducing ovarian reserve. To mitigate this gonadotoxicity, various emerging strategies are being explored, including kinase inhibitors, PI3K/Akt/mTOR pathway inhibitors, antioxidants, miRNAs and GnRH agonists. These treatments work by preventing follicular apoptosis or excessive activation of primordial follicles. Although promising results have been observed in vitro and in vivo in rodent models, further investigations to bypass their limitations are needed to confirm their efficacy and safety. These challenges include the noninterference with anti-tumoral effect of chemotherapy and the specificity of fertoprotective agents to ovaries.
引用
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页数:10
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