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口服肠炎沙门氏菌11RX感染对1,2 - 二甲基肼诱导小鼠结肠肿瘤的保护作用。

Protective effect of oral Salmonella enteritidis 11RX infection against colon tumor induction by 1,2-dimethylhydrazine in mice.

作者信息

Ashman L K, Cook M G, Kotlarski I

出版信息

Cancer Res. 1979 Jul;39(7 Pt 1):2768-71.

PMID:376122
Abstract

Infection of mice with Salmonella enteritidis 11RX has been shown previously to cause nonspecific immune stimulation and, consequently, resistance to subsequent challenge with a variety of transplantable tumors. The present study has examined the effect of infection with this organism in a chemical carcinogenesis system. Colonic tumors were induced in LACA and BALB/c x C57BL/6JF1 mice by weekly s.c. injection of 1,2-dimethylhydrazine (15 mg/kg) for 28 weeks. Infection of mice p.o. with live S. enteritidis 11RX at 8-week intervals during 1,2-dimethylhydrazine administration protected both strains against colon tumorigenesis. Significantly fewer infected than control BALB/c x C57BL/6JF1 mice had colonic tumors at or before termination of the experiment (34 or 40 weeks) (p less than 0.001 in all cases). Comparable results were obtained with both male and female mice. The difference in tumor incidence between control and infected LACA mice was not statistically significant, however; the number and size of the lesions was greater in control mice (p less than 0.02). Although it has not been proven that the protective effect is mediated by the immune system, the results are consistent with the operation of a macrophage-mediated surveillance system. It is suggested that enteric infections should be considered as a possible contributing factor in the epidemiology of human colonic cancer.

摘要

先前已表明,用肠炎沙门氏菌11RX感染小鼠会引起非特异性免疫刺激,因此能抵抗随后多种可移植肿瘤的攻击。本研究检测了该细菌感染在化学致癌系统中的作用。通过每周皮下注射1,2 - 二甲基肼(15毫克/千克),持续28周,在LACA和BALB/c x C57BL/6JF1小鼠中诱导结肠肿瘤。在给予1,2 - 二甲基肼期间,每隔8周经口用活的肠炎沙门氏菌11RX感染小鼠,可使这两种品系的小鼠均免受结肠肿瘤发生的影响。在实验结束时(34周或40周)及之前,感染组的BALB/c x C57BL/6JF1小鼠发生结肠肿瘤的数量明显少于对照组(所有情况下p均小于0.001)。雄性和雌性小鼠均得到了类似结果。然而,对照和感染的LACA小鼠之间肿瘤发生率的差异无统计学意义;对照组小鼠的病变数量和大小更大(p小于0.02)。尽管尚未证实这种保护作用是由免疫系统介导的,但结果与巨噬细胞介导的监测系统的作用一致。有人提出,肠道感染应被视为人类结肠癌流行病学中一个可能的促成因素。

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Cancer Res. 1979 Jul;39(7 Pt 1):2768-71.
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1
Rodent models for carcinoma of the colon.结肠癌的啮齿动物模型。
Dig Dis Sci. 1985 Dec;30(12 Suppl):87S-102S. doi: 10.1007/BF01296986.