Steffen Ann-Charlott, Göstring Lovisa, Tolmachev Vladimir, Palm Stig, Stenerlöw Bo, Carlsson Jörgen
Department of Oncology, Radiology and Clinical Immunology, Rudbeck Laboratory, Uppsala University, Uppsala, 751 85, Sweden.
Eur J Nucl Med Mol Imaging. 2008 Jun;35(6):1179-91. doi: 10.1007/s00259-007-0713-x. Epub 2008 Jan 12.
HER2 is a potential target for radionuclide therapy, especially when HER2 overexpressing breast cancer cells are resistant to Herceptin(R) treatment. Therefore, it is of interest to analyse whether HER2 overexpressing tumour cells have different inherent radiosensitivity.
The radiosensitivity of three often used HER2 overexpressing cell lines, SKOV-3, SKBR-3 and BT-474, was analysed. The cells were exposed to conventional photon irradiation, low linear energy transfer (LET), to characterise their inherent radiosensitivity. The analysis was made with clonogenic survival and growth extrapolation assays. The cells were also exposed to alpha particles, high LET, from (211)At decays using the HER2-binding affibody molecule (211)At-(Z(HER2:4))(2) as targeting agent. Assays for studies of internalisation of the affibody molecule were applied.
SKOV-3 cells were most radioresistant, SKBR-3 cells were intermediate and BT-474 cells were most sensitive as measured with the clonogenic and growth extrapolation assays after photon irradiation. The HER2 dependent cellular uptake of (211)At was qualitatively similar for all three cell lines. However, the sensitivity to the alpha particles from (211)At differed; SKOV-3 was most resistant, SKBR-3 intermediate and BT-474 most sensitive. These differences were unexpected because it is assumed that all types of cells should have similar sensitivity to high-LET radiation. The sensitivity to alpha particle exposure correlated with internalisation of the affibody molecule and with size of the cell nucleus.
There can be differences in radiosensitivity, which, if they also exist between patient breast cancer cells, are important to consider for both conventional radiotherapy and for HER2-targeted radionuclide therapy.
HER2是放射性核素治疗的一个潜在靶点,尤其是当HER2过表达的乳腺癌细胞对赫赛汀治疗耐药时。因此,分析HER2过表达的肿瘤细胞是否具有不同的固有放射敏感性具有重要意义。
分析了三种常用的HER2过表达细胞系SKOV-3、SKBR-3和BT-474的放射敏感性。将细胞暴露于传统的光子辐射(低线性能量传递,LET)下,以表征其固有放射敏感性。采用克隆形成存活和生长外推法进行分析。细胞还暴露于使用HER2结合亲和分子(211)At-(Z(HER2:4))2作为靶向剂的(211)At衰变产生的α粒子(高线性能量传递,LET)下。应用了亲和分子内化研究的分析方法。
光子照射后,用克隆形成和生长外推法测量,SKOV-3细胞放射抗性最强,SKBR-3细胞居中,BT-474细胞最敏感。所有三种细胞系对(211)At的HER2依赖性细胞摄取在性质上相似。然而,对(211)At产生的α粒子的敏感性不同;SKOV-3抗性最强,SKBR-3居中,BT-474最敏感。这些差异出乎意料,因为通常认为所有类型的细胞对高LET辐射应具有相似的敏感性。对α粒子暴露的敏感性与亲和分子的内化以及细胞核大小相关。
放射敏感性可能存在差异,如果患者乳腺癌细胞之间也存在这种差异,那么在传统放疗和HER2靶向放射性核素治疗中都需要加以考虑。