首页|微RNA-93-5p对多囊卵巢综合征患者卵巢颗粒细胞增殖的影响及机制

微RNA-93-5p对多囊卵巢综合征患者卵巢颗粒细胞增殖的影响及机制

Effect and mechanism of microRNA-93-5p on ovarian granulosa cell proliferation in patients with polycystic ovary syndrome

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目的 探讨血浆微RNA(miR)-93-5p对多囊卵巢综合征(PCOS)患者卵巢颗粒细胞增殖的影响及其可能机制.方法 选择2022年1月至2023年1月焦作市人民医院收治的120例育龄期PCOS患者为PCOS组,选择同期在本院体检的18例育龄期健康女性为对照组.收集2组受试者的年龄、体质量和身高,计算体质量指数(BMI).2组受试者均在自然月经周期的卵泡期或黄体酮诱导的撤退性出血期采集空腹静脉血,采用电化学法测定血清黄体生成素(LH)、促卵泡激素(FSH)、总睾酮(TT)、抗米勒管激素(AMH)、天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)、空腹胰岛素(FINS)、空腹血糖(FBG)水平,并计算胰岛素抵抗稳态模型(HOMA-IR);采用实时荧光定量聚合酶链反应(qRT-PCR)检测2组受试者血浆中 miR-93-5p表达水平.取对数生长期人卵巢颗粒细胞KGN,以每孔3 × 105个细胞接种至 6 孔板中,随机分为 miR-93-5p mimics 组、LY294002+miR-93-5p 组、AZD5363+miR-93-5p 组、阴性对照(NC)组、空白对照组.miR-93-5p 组 KGN 细胞转染 miR-93-5p mimics;LY294002+miR-93-5p 组 KGN 细胞转染 miR-93-5p mimics,并于转染前 1 h 给予 50 mmol·L-1 LY294002 处理;AZD5363+miR-93-5p 组 KGN 细胞转染 miR-93-5p mimics,并于转染前1 h给予50 μmol·L-1 AZD5363处理;NC组KGN细胞转染阴性对照质粒;空白对照组KGN细胞不做任何处理.应用qRT-PCR法检测各组KGN细胞中miR-93-5p表达,细胞计数试剂盒-8试验检测各组KGN细胞增殖情况.结果 PCOS组与对照组受试者的年龄及FSH、ALT、AST水平比较差异无统计学意义(P>0.05);PCOS组患者的BMI、TT、AMH、LH、FINS、FBG、HOMA-IR显著高于对照组(P<0.05).PCOS组患者血浆中miR-93-5p相对表达量显著高于对照组(t=-5.549,P<0.001).miR-93-5p 与 TT、FINS、HOMA-IR 呈中度正相关(r=0.434、0.622、0.586,P<0.001),与 FBG 和 LH 呈低度正相关(r=0.398、0.398,P<0.001).ROC 曲线显示,血浆 miR-93-5p 诊断 PCOS 的最佳临界值为1.380,曲线下面积为0.906(95%置信区间:0.839~0.973,P<0.001),敏感度为0.858,特异度为0.833,约登指数为 0.691.miR-93-5p mimics 组、LY294002+miR-93-5p 组、AZD5363+miR-93-5p 组 KGN 细胞中miR-93-5p相对表达量均显著高于空白对照组和NC组(P<0.05).培养24、48、72 h时,miR-93-5p mimics组、LY294002+miR-93-5p组、AZD5363+miR-93-5p组KGN细胞的增殖能力显著高于空白对照组和NC组(P<0.05);LY294002+miR-93-5p 组、AZD5363+miR-93-5p 组细胞的增殖能力显著低于 miR-93-5p mimics 组(P<0.05).结论 PCOS患者血浆miR-93-5p呈过表达,miR-93-5p可能通过基于调控磷脂酰肌醇-3-激酶/蛋白激B信号通路介导PCOS卵巢颗粒细胞增殖来参与PCOS的发生发展,血浆miR-93-5p水平对PCOS有一定的诊断价值.
Objective To investigate the effect of plasma microRNA(miR)-93-5p on ovarian granulosa cell proliferation in patients with polycystic ovary syndrome(PCOS)and its possible mechanism.Methods A total of 120 PCOS patients of childbearing period who were treated at Jiaozuo People's Hospital from January 2022 to January 2023 were selected as the PCOS group,and 18 healthy women of childbearing period who were physically examined at the same hospital during the same period were selected as the control group.The age,body weight and height of the subjects in the two groups were recorded,and the body mass index(BMI)was calculated.Fasting venous blood was collected from the subjects during the follicular phase of the natural menstrual cycle or the progesterone-induced withdrawal bleeding phase,and serum levels of luteinizing hormone(LH),follicle-stimulating hormone(FSH),total testosterone(TT),anti-Mullerian hormone(AMH),aspartate aminotransferase(AST),alanine aminotransferase(ALT),fasting insulin(FINS),and fasting blood glucose(FBG)were measured by using the electrochemical method;and the homeostasis model assessment of insulin resistance(HOMA-IR)was calculated.Quantitative real-time polymerase chain reaction(qRT-PCR)was used to detect the expression level of miR-93-5p in plasma of patients in the two groups.Human ovarian granulosa cells(KGN cells)in logarithmic growth phase were cultured in 6-well plates with 3 × 105 cells per well,and they were randomly divided into the miR-93-5p mimics group,LY294002+miR-93-5p group,AZD5363+miR-93-5p group,negative control(NC)group,and blank control group.The KGN cells in the miR-93-5p group were transfected with miR-93-5p mimics;the KGN cells in the LY294002+miR-93-5p group were transfected with miR-93-5p mimics and treated with 50 mmol·L-1 LY294002 one hour before transfection;the KGN cells in the AZD5363+miR-93-5p group were transfected with miR-93-5p mimics and treated with 50 μmol·L-1 AZD5363 one hour before transfection;the KGN cells in the NC group were transfected with the negative control plasmids;and the KGN cells in the blank control group were not treated at all.The expression of miR-93-5p in the KGN cells in each group was detected by qRT-PCR,and the proliferation of the KGN cells in each group was detected by cell counting kit-8.Results There was no significant differences in age,FSH,ALT,and AST levels of patients between the PCOS group and the blank control group(P>0.05).The BMI,TT,AMH,LH,FINS,FBG,and HOMA-IR of patients in the PCOS group were significantly higher than those in the blank control group(P<0.05).The relative expression of miR-93-5p in plasma of patients in the PCOS group was significantly higher than that in the blank control group(t=-5.549,P<0.001).miR-93-5p was moderately positively correlated with TT,FINS and HOMA-IR(r=0.434,0.622,0.586;P<0.001)and was mildly positively correlated with FBG and LH(r=0.398,0.398;P<0.001).The receiver operating characteristic curve showed that the optimal cut-off value for plasma miR-93-5p in diagnosing PCOS was 1.380,the area under the curve was 0.906(95%confidence interval:0.839-0.973,P<0.001),the sensitivity was 0.858,the specificity was 0.833,and the Youden index was 0.691.The relative expression of miR-93-5p in the KGN cells in the miR-93-5p mimics group,LY294002+miR-93-5p group and AZD5363+miR-93-5p group was significantly higher than that in the blank control group and NC group(P<0.05).After 24,48 and 72 hours of culture,the proliferation of the KGN cells in the miR-93-5p mimics group,LY294002+miR-93-5p group and AZD5363+miR-93-5p group was significantly higher than that in the blank control group and the NC group(P<0.05);the proliferation of the KGN cells in the LY294002+miR-93-5p group and AZD5363+miR-93-5p group was significantly lower than that in the miR-93-5p mimics group(P<0.05).Conclusion miR-93-5p in plasma is overexpressed in PCOS patients,and it may be involved in the occurrence and development of PCOS by mediating the proliferation of ovarian granulosa cells through the phosphoinositide 3 kinase/protein kinase B signaling pathway.The miR-93-5p level in plasma has a certain diagnostic value for PCOS.

polycystic ovary syndromeovarian granulosa cellsmicroRNA-93-5pproliferation

王敬敏、李卫、闫佳敏、赵凯、张慧、刘莹、任一梦、金帅、韩丹

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焦作市人民医院妇产科,河南 焦作 454000

焦作市人民医院核医学科,河南 焦作 454000

焦作市人民医院腹部彩超室,河南 焦作 454000

焦作市人民医院检验医学科,河南 焦作 454000

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多囊卵巢综合征 卵巢颗粒细胞 微RNA-93-5p 增殖

2024

新乡医学院学报
新乡医学院

新乡医学院学报

CSTPCD
影响因子:0.999
ISSN:1004-7239
年,卷(期):2024.41(6)