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电离辐射在小鼠皮肤肿瘤形成的两阶段模型中作为引发剂。

Ionizing radiation as an initiator in the mouse two-stage model of skin tumor formation.

作者信息

Jaffe D R, Bowden G T

出版信息

Radiat Res. 1986 May;106(2):156-65.

PMID:3704109
Abstract

The initiating potential of a range (7.5 to 22.5 Gy) of 4 MeV X rays was studied using the mouse skin two-stage model of carcinogenesis. A single dose of radiation was followed by 60 weeks of promotion with 12-O-tetradecanoyl phorbol-13-acetate (TPA) (8 nmol, two times per week). Since the proliferative state of a target cell population is known to influence carcinogen-induced tumorigenesis, we also investigated the effect of TPA on tumor incidence when applied as a single dose (17 nmol) 24 h prior to irradiation. Evidence presented here indicates that ionizing radiation can act as an initiator in this model system. All groups of animals that were promoted with TPA developed papillomas regardless of radiation treatment; however, only those groups of animals that received irradiation followed by TPA promotion developed squamous cell carcinomas. The incidence of nonepidermal tumors was similar between all radiation dose groups and was independent of TPA promotion. Our results also indicate that TPA pretreatment prior to irradiation results in an overall increase in the total tumor incidence, including both epidermal and nonepidermal tumors.

摘要

使用小鼠皮肤致癌作用两阶段模型,研究了4兆电子伏X射线在7.5至22.5戈瑞剂量范围内的启动潜力。单次辐射剂量后,用12-O-十四烷酰佛波醇-13-乙酸酯(TPA)(8纳摩尔,每周两次)进行60周的促癌处理。由于已知靶细胞群体的增殖状态会影响致癌物诱导的肿瘤发生,我们还研究了在照射前24小时单次给予TPA(17纳摩尔)时其对肿瘤发生率的影响。此处提供的证据表明,在该模型系统中电离辐射可作为启动剂。所有用TPA促癌的动物组均发生了乳头状瘤,无论是否接受辐射处理;然而,只有那些先接受照射然后用TPA促癌的动物组发生了鳞状细胞癌。所有辐射剂量组中非表皮肿瘤的发生率相似,且与TPA促癌无关。我们的结果还表明,照射前进行TPA预处理会导致包括表皮和非表皮肿瘤在内的总肿瘤发生率总体增加。

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