Can we really protect the ovary from chemotherapy damage?
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作者:
Nguyen, Thuy Truong An
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Univ Libre Bruxelles ULB, Fac Med, Res Lab Human Reprod, B-1070 Brussels, BelgiumUniv Libre Bruxelles ULB, Fac Med, Res Lab Human Reprod, B-1070 Brussels, Belgium
Nguyen, Thuy Truong An
[1
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Condorelli, Margherita
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HUB Erasme, Fertil Clin, Dept Obstet & Gynecol, Brussels, BelgiumUniv Libre Bruxelles ULB, Fac Med, Res Lab Human Reprod, B-1070 Brussels, Belgium
Condorelli, Margherita
[2
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Demeestere, Isabelle
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Univ Libre Bruxelles ULB, Fac Med, Res Lab Human Reprod, B-1070 Brussels, Belgium
HUB Erasme, Fertil Clin, Dept Obstet & Gynecol, Brussels, BelgiumUniv Libre Bruxelles ULB, Fac Med, Res Lab Human Reprod, B-1070 Brussels, Belgium
Demeestere, Isabelle
[1
,2
]
机构:
[1] Univ Libre Bruxelles ULB, Fac Med, Res Lab Human Reprod, B-1070 Brussels, Belgium
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.