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Human Neural Stem Cells Can Target and Deliver Therapeutic Genes to Breast Cancer Brain Metastases

机译:人类神经干细胞可以靶向并向乳腺癌脑转移提供治疗基因

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摘要

The tumor-tropic properties of neural stem cells (NSCs) led to the development of a novel strategy for delivering therapeutic genes to tumors in the brain. To apply this strategy to the treatment of brain metastases, we made a human NSC line expressing cytosine deaminase (F3.CD), which converts 5-fluorocytosine (5-FC) into 5-fluorouracil, an anticancer agent. In vitro, the F3.CD cells significantly inhibited the growth of tumor cell lines in the presence of the prodrug 5-FC. In vivo, MDA-MB-435 human breast cancer cells were implanted into the brain of immune-deficient mouse stereotactically, and F3.CD cells were injected into the contralateral hemisphere followed by systemic 5-FC administration. The F3.CD cells migrated selectively into the brain metastases located in the opposite hemisphere and resulted in significantly reduced volumes. The F3.CD and 5-FC treatment also decreased both tumor volume and number of tumor mass significantly, when immune-deficient mouse had MDA-MB-435 cells injected into the internal carotid artery and F3.CD cells were transplanted into the contralateral brain hemisphere stereotactically. Taken together, brain transplantation of human NSCs, encoding the suicide enzyme CD, combined with systemic administration of the prodrug 5-FC, is an effective treatment regimen for brain metastases of tumors.
机译:神经干细胞(NSC)的肿瘤嗜性特性导致开发了一种新的策略,可将治疗性基因传递给脑部肿瘤。为了将该策略应用于脑转移瘤的治疗,我们制备了表达胞嘧啶脱氨酶(F3.CD)的人NSC系,该系将5-氟胞嘧啶(5-FC)转化为抗癌药5-氟尿嘧啶。在体外,在前药5-FC存在下,F3.CD细胞可显着抑制肿瘤细胞系的生长。在体内,将MDA-MB-435人乳腺癌细胞立体定向植入到免疫缺陷小鼠的大脑中,然后将F3.CD细胞注入对侧半球,然后进行全身5-FC给药。 F3.CD细胞选择性迁移到对侧半球的脑转移瘤中,导致体积明显减少。当免疫缺陷的小鼠将MDA-MB-435细胞注入颈内动脉并将F3.CD细胞移植到对侧脑中时,F3.CD和5-FC处理也显着降低了肿瘤体积和肿瘤块数。在立体上半球。综上所述,编码自杀酶CD的人NSC的脑移植与前药5-FC的全身给药相结合,是治疗肿瘤脑转移的有效疗法。

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