Misao R, Nakanishi Y, Ichigo S, Hori M, Fujimoto J, Tamaya T
Department of Obstetrics and Gynecology, Gifu University School of Medicine, Japan.
J Steroid Biochem Mol Biol. 1995 Jun;52(6):517-22. doi: 10.1016/0960-0760(95)00061-4.
To more fully understand the role of sex hormone-binding globulin (SHBG) on the intracellular steroidal action in endometrial cancers, we investigated the expression of SHBG mRNA as the substitute of SHBG expression in human endometrial cancers. In the present study, the levels of SHBG mRNA were analyzed using competitive reverse transcription-polymerase chain reaction (RT-PCR)-Southern-blot analysis. The higher level of SHBG mRNA tended to be expressed in the normal secretory and late proliferative phase endometrium > early proliferative phase endometrium > well differentiated adenocarcinoma of the endometrium (G1) > moderately differentiated adenocarcinoma (G2) > poorly differentiated adenocarcinoma (G3), in the order shown. These studies indicate that endometrial cancer cells might synthesize intracellular SHBG to conserve their estrogen-dependent properties. Further, it indicates that endometrial cancer cell synthesis of SHBG mRNA is lost as these cells undergo de-differentiation.
为了更全面地了解性激素结合球蛋白(SHBG)在子宫内膜癌细胞内甾体作用中的作用,我们研究了SHBG mRNA的表达,以此作为人子宫内膜癌中SHBG表达的替代指标。在本研究中,采用竞争性逆转录 - 聚合酶链反应(RT-PCR)-Southern印迹分析法分析SHBG mRNA水平。SHBG mRNA水平倾向于按以下顺序表达:正常分泌期和增殖晚期子宫内膜>增殖早期子宫内膜>高分化子宫内膜腺癌(G1)>中分化腺癌(G2)>低分化腺癌(G3)。这些研究表明,子宫内膜癌细胞可能合成细胞内SHBG以维持其雌激素依赖性特性。此外,这表明随着这些细胞去分化,SHBG mRNA的子宫内膜癌细胞合成会丧失。