Overactivation or Apoptosis: Which Mechanisms Affect Chemotherapy-Induced Ovarian Reserve Depletion?

被引:10
作者
Kashi, Oren [1 ]
Meirow, Dror [1 ,2 ]
机构
[1] Sheba Med Ctr, Morris Kahn Fertil Preservat Ctr, IL-5262000 Ramat Gan, Israel
[2] Tel Aviv Univ, Fac Med, IL-6997801 Tel Aviv, Israel
关键词
ovary; primordial follicle; apoptosis; activation; premature ovarian insufficiency; ovarian reserve; chemotherapy; ANTI-MULLERIAN HORMONE; HIPPO SIGNALING DISRUPTION; PROTECTS MOUSE OOCYTES; PRIMORDIAL FOLLICLES; DNA-DAMAGE; FERTILITY PRESERVATION; ACTIVATION; CANCER; CYCLOPHOSPHAMIDE; INHIBITION;
D O I
10.3390/ijms242216291
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dormant primordial follicles (PMF), which constitute the ovarian reserve, are recruited continuously into the cohort of growing follicles in the ovary throughout female reproductive life. Gonadotoxic chemotherapy was shown to diminish the ovarian reserve pool, to destroy growing follicle population, and to cause premature ovarian insufficiency (POI). Three primary mechanisms have been proposed to account for this chemotherapy-induced PMF depletion: either indirectly via over-recruitment of PMF, by stromal damage, or through direct toxicity effects on PMF. Preventative pharmacological agents intervening in these ovotoxic mechanisms may be ideal candidates for fertility preservation (FP). This manuscript reviews the mechanisms that disrupt follicle dormancy causing depletion of the ovarian reserve. It describes the most widely studied experimental inhibitors that have been deployed in attempts to counteract these affects and prevent follicle depletion.
引用
收藏
页数:18
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