Department of Obstetrics and Gynecology, Private Konya Anıt Hospital, Konya, Turkey.
Başaran Clinic, Konya, Turkey.
Turk J Med Sci. 2023 Feb;53(1):149-159. doi: 10.55730/1300-0144.5568. Epub 2023 Feb 22.
Laminin-1 and matrix metalloproteinase (MMP)-9 may play roles in the progression from benign to malignant endometrium, so we aimed to investigate their levels of expression in these tissues.
This case-control study was conducted at a tertiary care center between January 2014 and December 2016. Paraffin blocks of 50 specimens of benign endometrium with proliferative (n = 20), secretory (n = 11), and atrophic (n = 5) endometrium; simple endometrial hyperplasia without atypia (n = 12); and endometrial polyp (n = 2) histology and 49 specimens of malignant endometrium with endometrioid (n = 40), serous (n = 7), clear cell (n = 1), and undifferentiated (n = 1) types were immunostained with laminin-1 and MMP-9 antibodies and assessed for basement membrane continuity for laminin-1 and the percentage and intensity of MMP-9 expression in epithelial cytoplasm.
: Laminin-1 continuity in the basement membrane was higher in benign (92%) compared to malignant (16.3%) endometrium (p < 0.0001) without any difference between the subgroups within each group (p > 0.05). All atrophic endometria and endometrial polyps and 23.5% of low grade endometrioid and none of the other endometrial cancers showed uninterrupted basement membrane staining with laminin-1. All cases in malignant endometrium expressed MMP-9 with either low or high immunoreactivity while none of the cases in benign endometrium showed a high staining with MMP-9 (p < 0.01). Proliferative and hyperplastic endometrium together with grade 1 endometrioid cancer expressed MMP-9 better than the atrophic endometrium (p < 0.05). The immunoreactivity with MMP-9 increased gradually from secretory to hyperplastic endometrium and serous carcinoma (p < 0.05). MMP-9 expression in all types of cancers except grade 1 endometrioid and clear cell compared to proliferative endometrium was significantly higher (p < 0.05) and increased from proliferative to grade 2 endometrioid, grade 3 endometrioid, serous and undifferentiated endometrial carcinoma.
Gradual increments in MMP-9 expression and basement membrane laminin-1 discontinuity may indicate progression from normal to hyperplastic and to low- and high-grade cancerous endometrium.
层粘连蛋白-1 和基质金属蛋白酶(MMP)-9 可能在良性子宫内膜向恶性子宫内膜的进展中发挥作用,因此我们旨在研究这些组织中它们的表达水平。
本病例对照研究于 2014 年 1 月至 2016 年 12 月在一家三级保健中心进行。石蜡块 50 例,良性子宫内膜组织,增生期(n = 20)、分泌期(n = 11)和萎缩期(n = 5);单纯性子宫内膜增生无不典型(n = 12);子宫内膜息肉(n = 2)组织学和 49 例恶性子宫内膜组织,子宫内膜样(n = 40)、浆液性(n = 7)、透明细胞(n = 1)和未分化(n = 1)型,用层粘连蛋白-1 和 MMP-9 抗体进行免疫染色,并评估层粘连蛋白-1 基底膜连续性和上皮细胞质中 MMP-9 表达的百分比和强度。
良性子宫内膜(92%)的层粘连蛋白-1 基底膜连续性高于恶性子宫内膜(16.3%)(p < 0.0001),但每组内各亚组之间无差异(p > 0.05)。所有萎缩性子宫内膜和子宫内膜息肉以及 23.5%的低级别子宫内膜样癌均表现为层粘连蛋白-1 基底膜无中断染色。所有恶性子宫内膜病例均表达 MMP-9,低或高免疫反应性,而良性子宫内膜病例均无高 MMP-9 染色(p < 0.01)。增生期和增生期子宫内膜与 1 级子宫内膜样癌一起表达 MMP-9 优于萎缩期子宫内膜(p < 0.05)。MMP-9 免疫反应性从分泌期到增生期和浆液性癌逐渐增加(p < 0.05)。除 1 级子宫内膜样癌和透明细胞癌外,所有类型癌症的 MMP-9 表达均明显高于增生期子宫内膜(p < 0.05),并从增生期到 2 级子宫内膜样癌、3 级子宫内膜样癌、浆液性和未分化子宫内膜癌逐渐增加。
MMP-9 表达和基底膜层粘连蛋白-1 不连续性的逐渐增加可能表明从正常到增生期和低级别和高级别癌性子宫内膜的进展。