Pathological features of the colonic tumours induced in rats by the administration of 1,2-dimethylhydrazine.

J P Sunter, D R Appleton, N A Wright, A J Watson
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引用次数: 64

Abstract

The parenteral administration of 1,2-dimethylhydrazine to rats caused the development of colonic neoplasms in about 90% of animals by 24--30 weeks of treatment. Usually there were multiple tumours with a mean of 2.7 per rat. The lesions have been classified histologically into adenomata (26% of all tumours) and carcinomata, the latter showing varying degrees of differentiation. No completely anaplastic tumours were seen, and there were none originating in connective tissue. The distributions of the different tumour types along the length of the colon varied. The more benign lesions were situated predominantly in the distal half of the colon, while the poorly differentiated adenocarcinomata were concentrated in the proximal third of the colon. There was good evidence to suggest that adenomata often progressed to frank malignancy in the distal colon. In the proximal part, however, it appeared that tumours frequently developed de novo as poorly differentiated carcinomata. Perhaps regional variations in the kinetic organisation of the normal colonic mucosa somehow influence the nature of the neoplastic change induced by DMH, thus accounting for the differences in tumor distribution. After 24 weeks of DMH treatment there was only a small increase in the mean number of tumours per rat.

1,2-二甲基肼诱导大鼠结肠肿瘤的病理特征。
大鼠经肠外注射1,2-二甲基肼,在治疗24- 30周后,约90%的动物发生结肠肿瘤。通常有多个肿瘤,平均每只大鼠2.7个。病变在组织学上分为腺瘤(占所有肿瘤的26%)和癌,后者表现出不同程度的分化。未见完全间变性肿瘤,也未见起源于结缔组织的肿瘤。不同肿瘤类型沿结肠长度的分布不同。良性病变主要位于结肠远端一半,而低分化腺癌集中在结肠近端三分之一。有充分的证据表明腺瘤经常在远端结肠发展为明显的恶性肿瘤。然而,在近端,肿瘤似乎经常以低分化癌的形式重新发展。也许正常结肠粘膜动力组织的区域差异在某种程度上影响了DMH诱导的肿瘤变化的性质,从而解释了肿瘤分布的差异。DMH治疗24周后,每只大鼠的平均肿瘤数量只有小幅增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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