P. A. Hertsen Moscow Oncology Research Institute - Affiliated Branch of National Medical Research Radiological Centre, Ministry of Health of the Russian Federation, Moscow, Russia.
National Research Center Kurchatov Institute, Moscow, Russia.
Bull Exp Biol Med. 2021 Sep;171(5):627-632. doi: 10.1007/s10517-021-05283-4. Epub 2021 Oct 9.
Two radiopharmaceutical preparations were developed on the basis of artificial targeted polypeptide ZHER2 specific to HER2/neu tumor marker and radionuclides Lu (ZHER2-HSA-chelator-Lu) or Pb (ZHER2-HSA-chelator-Pb). The objective was to evaluate in vitro the cytotoxic activity of the targeted radiopharmaceuticals using two cultured human breast cancer cell lines with different expression of HER2/neu: SK-BR3 (high expression of HER2/neu) and MCF-7 (low expression of HER2/neu). It was shown that the cytotoxic effect of both preparations was significantly higher against the SK-BR-3 cells. The cytotoxicity correlated with the incubation period (it was higher after 72 h than after 24 h) and was significantly more pronounced in comparison with activity of radionuclide salts without a specific ligand. In vivo preclinical study of these pharmaceuticals seems to be very promising in animals with xenografted tumors showing high expression of HER2/neu marker.
基于针对 HER2/neu 肿瘤标志物的人工靶向多肽 ZHER2,开发了两种放射性药物制剂,并用放射性核素 Lu(ZHER2-HSA-配体-Lu)或 Pb(ZHER2-HSA-配体-Pb)进行标记。目的是使用两种具有不同 HER2/neu 表达的培养的人乳腺癌细胞系(SK-BR3[HER2/neu 高表达]和 MCF-7[HER2/neu 低表达]),体外评估靶向放射性药物的细胞毒性活性。结果表明,两种制剂对 SK-BR-3 细胞的细胞毒性作用均明显更高。细胞毒性与孵育时间相关(72 h 时比 24 h 时更高),与没有特异性配体的放射性核素盐的活性相比,其差异更为显著。在高表达 HER2/neu 标志物的异种移植肿瘤动物中进行这些药物的体内临床前研究似乎非常有前途。