Department of Gynecologic Oncology, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, Beijing, China.
Gynecol Obstet Invest. 2023;88(4):226-239. doi: 10.1159/000530460. Epub 2023 Jul 10.
The effect of telomerase inhibitor BIBR1532 on endometriotic cells was investigated to explore the inhibitory effect of targeting telomerase on endometriosis.
In vitro primary cell culture study. Participants/Materials: Primary endometrial cells derived from eutopic and ectopic endometrium in patients with endometriosis.
The study was conducted in the university hospital.
Paired eutopic and ectopic endometrial cells were collected from 6 patients from January 2018 to July 2021. A TRAP assay was performed to detect the telomerase activity of the cells. MTT, cell cycle, apoptosis, migration, and invasion assays were performed to study the inhibitory effect of BIBR1532. Enrichment analysis was performed to identify the key pathways involved in endometriosis progression and telomerase action. Then, Western blotting was used to investigate the expression of related proteins.
BIBR1532 treatment significantly inhibited the growth of eutopic and ectopic endometrial cells, with apoptosis and cell cycle signaling involved. Migration and invasion, important characteristics for the establishment of ectopic lesions, were also inhibited by BIBR1532. The MAPK signaling cascade, related to telomerase and endometriosis, was decreased in eutopic and ectopic endometrial stromal cells with the treatment of BIBR1532.
The severe side effects of telomerase inhibitors might be the main obstacle to clinical application, so it is necessary to find better drug delivery methods in vivo.
The telomerase inhibitor BIBR1532 affects endometrial cell proliferation, migration, and invasion in endometriosis.
研究端粒酶抑制剂 BIBR1532 对子宫内膜异位症细胞的作用,探索靶向端粒酶对子宫内膜异位症的抑制作用。
体外原代细胞培养研究。
参与者/材料:来源于子宫内膜异位症患者在位和异位子宫内膜的原代子宫内膜细胞。
大学医院。
收集 2018 年 1 月至 2021 年 7 月的 6 名患者的配对在位和异位子宫内膜细胞。进行 TRAP 分析检测细胞中端粒酶活性。通过 MTT、细胞周期、凋亡、迁移和侵袭实验研究 BIBR1532 的抑制作用。进行富集分析以鉴定涉及子宫内膜异位症进展和端粒酶作用的关键途径。然后,使用 Western blot 检测相关蛋白的表达。
BIBR1532 处理显著抑制了在位和异位子宫内膜细胞的生长,涉及细胞凋亡和细胞周期信号通路。BIBR1532 还抑制了迁移和侵袭,这是建立异位病变的重要特征。与端粒酶和子宫内膜异位症相关的 MAPK 信号级联在 BIBR1532 处理的在位和异位子宫内膜基质细胞中减少。
端粒酶抑制剂的严重副作用可能是其临床应用的主要障碍,因此有必要在体内寻找更好的药物输送方法。
端粒酶抑制剂 BIBR1532 影响子宫内膜异位症中子宫内膜细胞的增殖、迁移和侵袭。