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首页> 外文期刊>British Journal of Cancer >Facilitation of nodal metastasis from a non-immunogenic murine carcinoma by previous whole-body irradiation of tumour recipients
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Facilitation of nodal metastasis from a non-immunogenic murine carcinoma by previous whole-body irradiation of tumour recipients

机译:通过以前的肿瘤受体辐照从非免疫原鼠癌中促进Nodal转移

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Of 193 CBA mice kept under prolonged observation after excision of small intradermal transplants of a non-immunogenic tumour (CBA Carcinoma NT), 27 (14%) presented with local recurrence, 19 (10%) with regional lymphnodal metastasis (RNM) and 72 (37%), with pulmonary metastasis +/- other systemic metastases. When mice were exposed to sublethal whole-body irradiation (WBI) before tumour transplantation, the incidence of RNM rose to approximately 80% and the latent period was reduced from approximately 60 days to approximately 40 days after tumour transplantation. This enhancement of RNM by WBI was undiminished when the interval between WBI and tumour transplantation was increased from 1 to 90 days. An explanation for this effect in terms of immunosuppression by the WBI is unlikely for the following reasons: the tumour was non-immunogenic by standard quantitative tests, the effect persisted long after the expected time for recovery of immune reactivity, and i.v. injection of normal marrow and lymphoid cells after WBI failed to reduce the effect. That the effect was systemic was proved by failure of local pre-irradiation of the tumour bed or regional node to enhance RNM. The effect was not observed when WBI was given 4 days after excision of tumours. These and other experiments failed to indicate the mechanism of the effect of WBI, but its long persistence suggests that it may relate to stored lethal radiation damage in migrating cells of slow turnover tissues.
机译:在193年的CBA小鼠在切除非免疫原性肿瘤(CBA癌NT)的小皮内移植后长时间观察,27%(14%)呈现出局部复发,19(10%),区域淋巴结转移(RNM)和72 (37%),具有肺转移+/-其他全身转移。当小鼠暴露于肿瘤移植前的核心全体照射(WBI)时,RNM的发生率升至约80%,并且在肿瘤移植后约60天从大约60天降低潜伏期。当WBI增加WBI时,随着WBI和肿瘤移植的间隔从1至90天增加,这种增强了一定的。由于WBI的免疫抑制方面的这种效果的解释不太可能是以下原因:肿瘤通过标准定量试验是非免疫原性的,在预期的免疫反应性的预期时间后,效果长期持续存在,并且i.v。 WBI后未能降低效果后,注射正常骨髓和淋巴细胞。通过局部预照射肿瘤床或区域节点来增强RNM,证明了效果是系统性的。当肿瘤切除后4天给予WBI时,未观察到效果。这些和其他实验未能表明WBI效果的机制,但其长期持久性表明它可能与慢趋势组织的迁移细胞中的储存致命辐射损伤有关。

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