Li Juan, Yang Shou-jing, Zhao Xi-long, Zhang Ya-qing, Li Kai-nan, Cui Ji-hong, Li Jing
Department of Pathology, Fourth Military Medical University, Xi'an 710032, China.
Zhonghua Bing Li Xue Za Zhi. 2008 Feb;37(2):103-8.
To study the expression level and significance of glucose transporter 1 (Glut-1) in normal breast tissue, adenosis, adenoma and breast carcinoma.
A total of 147 cases of female breast tissue samples, including 92 cases of invasive ductal carcinoma, 26 cases of breast fibroadenoma, 24 cases of breast adenosis and 5 cases of normal breast tissues, were collected for quantitative detection of the expression of Glut-1 protein by immunohistochemistry (EnVision method) and Western blot, and its mRNA by reverse transcriptase-polymerase chain reaction (RT-PCR).
In normal breast tissue and benign lesions of the breast, Glut-1 was undetectable or only weakly detectable in cytoplasm of ductal and acinar epithelia. In contrast, the intensity of Glut-1 staining was significantly higher in invasive ductal carcinomas (P = 0.0002) with protein expression predominantly in cellular membrane and lesser in cytoplasm. Western blot and RT-PCR analyses showed that the expression of Glut-1 protein and mRNA were significantly increased in invasive ductal carcinoma than fibroadenoma (P =0.001 for protein; P <0.05 for mRNA) and adenosis (P =0.001 for protein; P < 0.05 for mRNA). There was a significant difference among groups (P = 0.0002 for protein; P = 0.0001 for mRNA).
Glucose transport activity, as indicated by Glut-1 protein and its mRNA expression, significantly increases in breast carcinoma than non-cancerous lesions. The over-expression of Glut-1 in breast carcinoma is tightly coupled with tumor cell proliferation, invasion and metastasis, implying that Glut-1 may serve as a new marker in the early diagnosis and prognostication of breast malignancy as well as a new therapeutic target.
研究葡萄糖转运蛋白1(Glut-1)在正常乳腺组织、乳腺腺病、乳腺腺瘤及乳腺癌中的表达水平及意义。
收集147例女性乳腺组织样本,其中浸润性导管癌92例、乳腺纤维腺瘤26例、乳腺腺病24例、正常乳腺组织5例,采用免疫组织化学(EnVision法)和蛋白质印迹法对Glut-1蛋白表达进行定量检测,采用逆转录聚合酶链反应(RT-PCR)检测其mRNA。
在正常乳腺组织及乳腺良性病变中,导管和腺泡上皮细胞质中Glut-1不可检测或仅微弱可检测。相比之下,浸润性导管癌中Glut-1染色强度显著更高(P = 0.0002),蛋白表达主要位于细胞膜,细胞质中较少。蛋白质印迹法和RT-PCR分析显示,浸润性导管癌中Glut-1蛋白和mRNA的表达显著高于纤维腺瘤(蛋白P = 0.001;mRNA P < 0.05)和腺病(蛋白P = 0.001;mRNA P < 0.05)。各组间存在显著差异(蛋白P = 0.0002;mRNA P = 0.0001)。
Glut-1蛋白及其mRNA表达所指示的葡萄糖转运活性在乳腺癌中比非癌性病变显著增加。乳腺癌中Glut-1的过表达与肿瘤细胞增殖、侵袭和转移密切相关,这意味着Glut-1可能作为乳腺恶性肿瘤早期诊断和预后评估的新标志物以及新的治疗靶点。