结直肠癌发展过程中的渐进式组织病理学改变

V. Nejati, Jamileh Abedi, M. Saatloo, Maryam Koohsoltani, R. Hobbenaghi, A. Tukmachi
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引用次数: 0

摘要

背景:结直肠癌是世界上最常见的死亡原因之一。目的:探讨结直肠癌发展过程中的组织病理学变化,包括高染、组织淋巴细胞浸润(TILs)、异常隐窝灶(ACF)、微血管密度(MVD)、p53、Bcl-2和CD31的变化。方法:大鼠皮下注射二甲肼DMH (40 mg/kg体重)10周。给药后第10、15、20、25、30、40周处死,每2只处死2只。薄石蜡切片进行抗cd31、抗bcl -2和抗p53染色。MVD和ACF作为三个hpf的平均值。结果:深染、TILs和血管新生是DMH治疗第10周最常见的初始组织学改变。深染的严重程度比其他变化增加得早,在第25周达到最高值。除TILs在第30周开始达到最高值并持续增加至第40周外,所有变异的最高值均出现在第40周。在第40周观察到p53的数量减少,而在第30至第40周观察到CD31和Bcl-2的强度增加。结论:TILs和血管生成可能是促进结直肠癌早期进展的重要因素。
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Gradual Histopathologic Changes During Development of Colorectal Cancer
Background: Colorectal cancer is one of the most common causes of mortality in the world. Objectives: The aim of this study was to investigate the histopathologic changes including hyperchromatism, tissue lymphocyte infiltrations (TILs), aberrant crypt foci (ACF), microvessel density (MVD), p53, Bcl-2 and CD31 changes during colorectal cancer development. Methods: Subcutaneous injections of dimethyl hydrazine DMH were administered to rats (40 mg/kg body weight) for 10 weeks. Rats were fed by food and water until 40th week and sacrificed two by two within 10, 15, 20, 25, 30 and 40 weeks after the start of treatment. Thin paraffinized sections were applied to anti-CD31, anti-Bcl-2 and anti-p53 staining procedures. MVD and ACF were reported as mean value of three HPFs. Results: Hyperchromatism, TILs and angiogenesis were the most common initial histologic changes which started at 10th week of DMH treatment. Hyperchromatism’s severity increased earlier than other changes and reached the highest value at the 25th week. The highest value of all variants occurred in the 40th week except the TILs which started to achieve the highest value in week 30 and increased until 40th week. A diminished amount of p53 was observed at week 40, however, increased intensity of CD31 and Bcl-2 were seen between 30th and 40th week. Conclusions: In conclusion, TILs and angiogenesis might be the important earliest factors contributing to colorectal cancer progression.
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