Kim Seongmin, Lee Sanghoon, Park Hyun-Tae, Song Jae-Yun, Kim Tak
Gynecologic Cancer Center, CHA Ilsan Medical Center, CHA University College of Medicine, 1205 Jungang-ro, Ilsandong-gu, Goyang-si 10414, Korea.
Department of Obstetrics and Gynecology, Korea University College of Medicine, 73 Inchon-ro, Seongbuk-gu, Seoul 02841, Korea.
Genes (Basel). 2021 Sep 28;12(10):1525. doi: 10.3390/genes12101525.
Chemotherapy-induced ovarian damage and fertility preservation in young patients with cancer are emerging disciplines. The mechanism of treatment-related gonadal damage provides important information for targeting prevention methods. The genomic aspects of ovarian damage after chemotherapy are not fully understood. Several studies have demonstrated that gene alterations related to follicular apoptosis or accelerated follicle activation are related to ovarian insufficiency and susceptibility to ovarian damage following chemotherapy. This may accelerate follicular apoptosis and follicle reservoir utilization and damage the ovarian stroma via multiple molecular reactions after chemotherapy. This review highlights the importance of genomic considerations in chemotherapy-induced ovarian damage and multidisciplinary oncofertility strategies for providing high-quality care to young female cancer patients.
化疗引起的卵巢损伤以及年轻癌症患者的生育力保存是新兴学科。治疗相关性腺损伤的机制为靶向预防方法提供了重要信息。化疗后卵巢损伤的基因组学方面尚未完全明确。多项研究表明,与卵泡凋亡或卵泡激活加速相关的基因改变与化疗后卵巢功能不全及卵巢损伤易感性有关。这可能会加速卵泡凋亡和卵泡储备的利用,并在化疗后通过多种分子反应损害卵巢基质。本综述强调了基因组学考量在化疗引起的卵巢损伤中的重要性,以及多学科肿瘤生育策略对于为年轻女性癌症患者提供高质量护理的重要性。