Department of Obstetrics and Gynecology, Bahcesehir University Goztepe Medicalpark Hospital, Istanbul, Turkey.
Department of Obstetrics and Gynecology, Gynolife Hospital, Nicosia, Cyprus.
Fertil Steril. 2023 Mar;119(3):504-513. doi: 10.1016/j.fertnstert.2022.11.021. Epub 2022 Dec 5.
To reveal whether hysteroscopic removal of the International Federation of Gynecology and Obstetrics (FIGO) types 0 and 1 fibroids makes any changes in the expression of homeobox genes (HOXA10, HOXA11), leukemia inhibitory factor, and nuclear factor-kappa B (NF-kB).
A case-control study.
University-based in vitro fertilisation center.
PATIENT(S): This study consisted of a total of 29 participants, 21 with FIGO types 0 and 1 fibroids and 8 with normal uterine cavity without fibroids.
INTERVENTION(S): Patients in FIGO types 0 and 1 fibroids group underwent hysteroscopic myomectomy. The patients in the control group underwent laparoscopic tubal ligation. Endometrial cells were collected by flushing method from all participants before and 3 months after myomectomy. Real-time polymerase chain reaction was used to detect HOXA10, HOXA11, and LIF mRNA expressions in endometrial flushing samples. The relative expressions of homeobox and LIF mRNA were calculated with comparative ΔCt method. Endometrial NF-kB concentration was measured quantitatively by enzyme-linked immunosorbent assay.
MAIN OUTCOME MEASURE(S): To compare endometrial HOXA10, HOXA11, and LIF mRNA expressions as well as endometrial NF-kB concentration before and after myomectomy.
RESULT(S): Premyomectomy NF-kB levels of type 0 (4.22 ± 1.02 ng/mL) and type 1 fibroid (6.44 ± 2.30 ng/mL) were significantly higher than the values of control group (0.54 ± 0.10 ng/mL). Surgical removal of type 0 and 1 fibroids resulted in a significant decrease in endometrial NF-kB levels (1.33 ± 0.02 ng/mL vs 1.65 ± 0.27 ng/mL, respectively). In type 0 fibroid group, after myomectomy, there was a 11.1-fold increase in HOXA10 mRNA, 4.23-fold in HOXA11 mRNA, and 7.63-fold in LIF mRNA. In the type 1 fibroid group, after myomectomy, there was a 16.3-fold increase in HOXA10 mRNA, 8.34-fold in HOXA11 mRNA, and 9.38-fold in LIF mRNA. A nonsignificant change was detected in homeobox and LIF mRNA after tubal sterilization. A negative and significant correlation was found between endometrial NF-kB and HOXA10 (r=-0.67), HOXA11 (r=-0.71) and LIF (r=-0.54).
CONCLUSION(S): High proinflammatory NF-kB concentration and low homeobox and LIF mRNA expressions were detected in the presence of type 0 or 1 fibroids that returned to normal values after hysteroscopic myomectomy.
揭示宫腔镜切除国际妇产科联合会(FIGO)0 型和 1 型肌瘤是否会改变同源盒基因(HOXA10、HOXA11)、白血病抑制因子和核因子-κB(NF-κB)的表达。
病例对照研究。
大学附属体外受精中心。
本研究共纳入 29 名参与者,21 名患有 FIGO 0 型和 1 型肌瘤,8 名患有无肌瘤的正常子宫腔。
FIGO 0 型和 1 型肌瘤组患者行宫腔镜子宫肌瘤切除术。对照组患者行腹腔镜输卵管结扎术。所有参与者在子宫肌瘤切除术前和术后 3 个月均采用冲洗法采集子宫内膜细胞。采用实时聚合酶链反应检测子宫内膜冲洗样本中 HOXA10、HOXA11 和 LIF mRNA 的表达。采用比较 ΔCt 法计算同源盒和 LIF mRNA 的相对表达。采用酶联免疫吸附试验定量测定子宫内膜 NF-κB 浓度。
比较子宫肌瘤切除术前和术后子宫内膜 HOXA10、HOXA11 和 LIF mRNA 表达及子宫内膜 NF-κB 浓度。
0 型(4.22±1.02ng/ml)和 1 型肌瘤(6.44±2.30ng/ml)术前 NF-κB 水平明显高于对照组(0.54±0.10ng/ml)。宫腔镜切除 0 型和 1 型肌瘤后,子宫内膜 NF-κB 水平明显下降(分别为 1.33±0.02ng/ml 和 1.65±0.27ng/ml)。在 0 型肌瘤组中,子宫肌瘤切除术后,HOXA10 mRNA 增加 11.1 倍,HOXA11 mRNA 增加 4.23 倍,LIF mRNA 增加 7.63 倍。在 1 型肌瘤组中,子宫肌瘤切除术后,HOXA10 mRNA 增加 16.3 倍,HOXA11 mRNA 增加 8.34 倍,LIF mRNA 增加 9.38 倍。输卵管绝育术后,同源盒和 LIF mRNA 无明显变化。子宫内膜 NF-κB 与 HOXA10(r=-0.67)、HOXA11(r=-0.71)和 LIF(r=-0.54)呈负相关。
0 型或 1 型肌瘤存在高促炎 NF-κB 浓度和低同源盒及 LIF mRNA 表达,宫腔镜切除后恢复正常。