Ogawa Kazuhiko, Boucher Yves, Kashiwagi Satoshi, Fukumura Dai, Chen David, Gerweck Leo E
Department of Radiation Oncology, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
Cancer Res. 2007 May 1;67(9):4016-21. doi: 10.1158/0008-5472.CAN-06-4498.
In this study, we evaluated the role of tumor cell and tumor stroma sensitivity as determinants of radiation-induced tumor growth delay. A DNA double-strand break repair-defective DNA-PKcs(-/-) tumor cell line and its radioresistant DNA-PKcs(+/+)-transfected counterpart were used to initiate tumors in nude and hypersensitive severe combined immunodeficient (SCID) mice. Insertion of the human DNA-PKcs(+/+) gene substantially increased the intrinsic radioresistance of the DNA-PKcs(-/-) tumor cells and substantially decreased tumor response to radiation in both nude and hypersensitive SCID mice. Tumor cell radiosensitivity was the major determinant of tumor response in nude mice. In SCID mice, both tumor cell sensitivity and radiation-induced stromal damage contributed to response. The relative contribution of host and tumor cell sensitivity on tumor response was unchanged for single doses of 1 x 15 and 6 x 3 Gy-fractionated dose irradiation.
在本研究中,我们评估了肿瘤细胞和肿瘤基质敏感性作为辐射诱导肿瘤生长延迟决定因素的作用。使用一种DNA双链断裂修复缺陷的DNA-PKcs(-/-)肿瘤细胞系及其具有放射抗性的DNA-PKcs(+/+)转染对应物,在裸鼠和超敏重症联合免疫缺陷(SCID)小鼠中引发肿瘤。人DNA-PKcs(+/+)基因的插入显著增加了DNA-PKcs(-/-)肿瘤细胞的内在放射抗性,并显著降低了裸鼠和超敏SCID小鼠中肿瘤对辐射的反应。肿瘤细胞放射敏感性是裸鼠中肿瘤反应的主要决定因素。在SCID小鼠中,肿瘤细胞敏感性和辐射诱导的基质损伤均对反应有影响。对于单次剂量1×15 Gy和6×3 Gy分割剂量照射,宿主和肿瘤细胞敏感性对肿瘤反应的相对贡献未发生变化。