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Evaluation of Lentiviral-Mediated Expression of Sodium Iodide Symporter in Anaplastic Thyroid Cancer and the Efficacy of In Vivo Imaging and Therapy

机译:慢病毒介导的碘化钠转运蛋白在间变性甲状腺癌中的表达及其体内显像和治疗的效果

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摘要

Anaplastic thyroid carcinoma (ATC) is one of the most deadly cancers. With intensive multimodalities of treatment, the survival remains low. ATC is not sensitive to 131I therapy due to loss of sodium iodide symporter (NIS) gene expression. We have previously generated a stable human NIS-expressing ATC cell line, ARO, and the ability of iodide accumulation was restored. To make NIS-mediated gene therapy more applicable, this study aimed to establish a lentiviral system for transferring hNIS gene to cells and to evaluate the efficacy of in vitro and in vivo radioiodide accumulation for imaging and therapy. Lentivirus containing hNIS cDNA were produced to transduce ARO cells which do not concentrate iodide. Gene expression, cell function, radioiodide imaging and treatment were evaluated in vitro and in vivo. Results showed that the transduced cells were restored to express hNIS and accumulated higher amount of radioiodide than parental cells. Therapeutic dose of 131I effectively inhibited the tumor growth derived from transduced cells as compared to saline-treated mice. Our results suggest that the lentiviral system efficiently transferred and expressed hNIS gene in ATC cells. The transduced cells showed a promising result of tumor imaging and therapy.
机译:间变性甲状腺癌(ATC)是最致命的癌症之一。随着密集的多模式治疗,存活率仍然很低。由于丢失了碘化钠共转运蛋白(NIS)基因表达,ATC对 131 I治疗不敏感。我们以前已经产生了稳定的表达人NIS的ATC细胞系ARO,并且碘化物积累的能力得以恢复。为了使NIS介导的基因治疗更适用,本研究旨在建立一种将hNIS基因转移至细胞的慢病毒系统,并评估体外和体内放射性碘化物积累对成像和治疗的功效。产生了包含hNIS cDNA的慢病毒以转导不浓缩碘化物的ARO细胞。在体外和体内评估基因表达,细胞功能,放射性碘显像和治疗。结果表明,与亲代细胞相比,转导的细胞得以恢复表达hNIS,并积累了更多的放射性碘。与生理盐水处理的小鼠相比, 131 I的治疗剂量可有效抑制转导细胞产生的肿瘤生长。我们的结果表明,慢病毒系统在ATC细胞中有效转移并表达了hNIS基因。转导的细胞显示了肿瘤成像和治疗的有希望的结果。

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