Knostman Katherine A B, McCubrey James A, Morrison Carl D, Zhang Zhaoxia, Capen Charles C, Jhiang Sissy M
Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio 43210, USA.
BMC Cancer. 2007 Jul 25;7:137. doi: 10.1186/1471-2407-7-137.
The sodium/iodide symporter (NIS) is a membrane glycoprotein mediating active iodide uptake in the thyroid gland and is the molecular basis for radioiodide imaging and therapeutic ablation of thyroid carcinomas. NIS is expressed in the lactating mammary gland and in many human breast tumors, raising interest in similar use for diagnosis and treatment. However, few human breast tumors have clinically evident iodide uptake ability. We previously identified PI3K signaling as important in NIS upregulation in transgenic mouse models of breast cancer, and the PI3K pathway is commonly activated in human breast cancer.
NIS expression, subcellular localization, and function were analyzed in MCF-7 human breast cancer cells and MCF-7 cells stably or transiently expressing PI3K p110alpha subunit using Western blot of whole cell lysate, cell surface biotinylation Western blot and immunofluorescence, and radioiodide uptake assay, respectively. NIS localization was determined in a human breast cancer tissue microarray using immunohistochemical staining (IHC) and was correlated with pre-existing pAkt IHC data. Statistical analysis consisted of Student's t-test (in vitro studies) or Fisher's Exact Test (in vivo correlational studies).
In this study, we demonstrate that PI3K activation in MCF-7 human mammary carcinoma cells leads to expression of underglycosylated NIS lacking cell surface trafficking necessary for iodide uptake ability. PI3K activation also appears to interfere with cell surface trafficking of exogenous NIS as well as all-trans retinoic acid-induced endogenous NIS. A correlation between NIS expression and upregulation of PI3K signaling was found in a human breast cancer tissue microarray.
Thus, the PI3K pathway likely plays a major role in the discordance between NIS expression and iodide uptake in breast cancer patients. Further study is warranted to realize the application of NIS-mediated radioiodide ablation in breast cancer.
钠/碘同向转运体(NIS)是一种膜糖蛋白,介导甲状腺中碘的主动摄取,是甲状腺癌放射性碘成像和治疗性消融的分子基础。NIS在哺乳期乳腺和许多人类乳腺肿瘤中表达,这引发了人们对其在诊断和治疗中类似应用的兴趣。然而,很少有人类乳腺肿瘤具有临床上明显的碘摄取能力。我们之前在乳腺癌转基因小鼠模型中确定PI3K信号在NIS上调中起重要作用,并且PI3K途径在人类乳腺癌中通常被激活。
分别使用全细胞裂解物的蛋白质印迹、细胞表面生物素化蛋白质印迹和免疫荧光以及放射性碘摄取试验,分析MCF-7人乳腺癌细胞和稳定或瞬时表达PI3K p110α亚基的MCF-7细胞中NIS的表达、亚细胞定位和功能。使用免疫组织化学染色(IHC)在人乳腺癌组织微阵列中确定NIS定位,并与预先存在的pAkt IHC数据相关联。统计分析包括学生t检验(体外研究)或Fisher精确检验(体内相关性研究)。
在本研究中,我们证明MCF-7人乳腺癌细胞中的PI3K激活导致糖基化不足的NIS表达,这种NIS缺乏碘摄取能力所需的细胞表面转运。PI3K激活似乎也干扰外源性NIS以及全反式维甲酸诱导的内源性NIS的细胞表面转运。在人乳腺癌组织微阵列中发现NIS表达与PI3K信号上调之间存在相关性。
因此,PI3K途径可能在乳腺癌患者中NIS表达与碘摄取不一致中起主要作用。有必要进行进一步研究以实现NIS介导的放射性碘消融在乳腺癌中的应用。