Background: 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.
Methods: 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 preexisting
pAkt IHC data. Statistical analysis consisted of Student's t-test (in vitro studies) or Fisher's
Exact Test (in vivo correlational studies).
Results: 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.
Conclusion: 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