Peters L J, Mason K, McBride W H, Patt Y Z
Radiology. 1978 Feb;126(2):499-505. doi: 10.1148/126.2.499.
The dynamics of 125IUdR-labeled tumor cell retention in the lungs have been compared with the efficiency of lung colony formation over a wide range of inoculum sizes in normal mice and in mice pretreated with 1000 rads local thoracic irradiation (LTI). These studies indicate that the increase in lung colony yield after LTI cannot be ascribed to improved intravascular trapping or interstitial lodgement of tumor cells. Hypotheses purporting that active specific or nonspecific host defense might be impaired by LTI were reassessed but rejected in favor of the idea that radiation-induced alterations in the physiological mocroenvironment of the lungs improve an intrinsically poor survival capability of intravenously disseminated tumor cells.
在正常小鼠和经1000拉德局部胸部照射(LTI)预处理的小鼠中,对125IUdR标记的肿瘤细胞在肺内滞留的动力学与在广泛接种量范围内肺集落形成效率进行了比较。这些研究表明,LTI后肺集落产量的增加不能归因于肿瘤细胞血管内捕获或间质滞留的改善。对认为LTI可能损害主动特异性或非特异性宿主防御的假说进行了重新评估,但被否决,转而支持这样一种观点,即辐射诱导的肺生理微环境改变改善了静脉播散肿瘤细胞原本较差的生存能力。