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N-甲基亚硝基脲(MNU)诱导的大鼠乳腺肿瘤中Myc表达上调。

Upregulated Myc expression in N-methyl nitrosourea (MNU)- induced rat mammary tumours.

作者信息

Barathidasan Rajamani, Pawaiya Rajveer Singh, Rai Ram Bahal, Dhama Kuldeep

机构信息

Division of Pathology, Indian Veterinary Research Institute, Izatnagar, India E-mail :

出版信息

Asian Pac J Cancer Prev. 2013;14(8):4883-9. doi: 10.7314/apjcp.2013.14.8.4883.

Abstract

BACKGROUND

The most common incident cancer and cause of cancer-related deaths in women is breast cancer. The Myc gene is upregulated in many cancer types including breast cancer, and it is considered as a potential anti-cancer drug target. The present study was conducted to evaluate the Myc (gene and protein) expression pattern in an experimental mammary tumour model in rats.

MATERIALS AND METHODS

Thirty six Sprague Dawley rats were divided into: Experimental group (26 animals), which received the chemical carcinogen N-methyl nitrosourea (MNU) and a control group (10 animals), which received vehicle only. c-Myc oncoprotein and its mRNA expression pattern were evaluated using immunohistochemistry (IHC) and semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR), respectively, in normal rat mammary tissue and mammary tumours. The rat glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene was used as internal control for semi-quantitative RT-PCR.

RESULTS

Histopathological examination of mammary tissues and tumours from MNU treated animals revealed the presence of premalignant lesions, benign tumours, in situ carcinomas and invasive carcinomas. Immunohistochemical evaluation of tumour tissues showed upregulation and heterogeneous cellular localization of c-Myc oncoprotein. The expression levels of c-Myc oncoprotein were significantly elevated (75- 91%) in all the tumours. Semi-quantitative RT-PCR revealed increased expression of c-Myc mRNA in mammary tumours compared to normal mammary tissues.

CONCLUSIONS

Further large-scale investigation study is needed to adopt this experimental rat mammary tumour model as an in vivo model to study anti-cancer strategies directed against Myc or its downstream partners at the transcriptional or post-transcriptional level.

摘要

背景

乳腺癌是女性中最常见的偶发癌症及癌症相关死亡原因。Myc基因在包括乳腺癌在内的多种癌症类型中上调,被认为是一个潜在的抗癌药物靶点。本研究旨在评估大鼠实验性乳腺肿瘤模型中Myc(基因和蛋白)的表达模式。

材料与方法

36只Sprague Dawley大鼠被分为:实验组(26只动物),接受化学致癌物N-甲基亚硝基脲(MNU);对照组(10只动物),仅接受赋形剂。分别使用免疫组织化学(IHC)和半定量逆转录聚合酶链反应(RT-PCR)评估正常大鼠乳腺组织和乳腺肿瘤中c-Myc癌蛋白及其mRNA的表达模式。大鼠甘油醛-3-磷酸脱氢酶(GAPDH)基因用作半定量RT-PCR的内参。

结果

对接受MNU处理动物的乳腺组织和肿瘤进行组织病理学检查,发现存在癌前病变、良性肿瘤、原位癌和浸润性癌。对肿瘤组织的免疫组织化学评估显示c-Myc癌蛋白上调且细胞定位不均一。所有肿瘤中c-Myc癌蛋白的表达水平均显著升高(75%-91%)。半定量RT-PCR显示,与正常乳腺组织相比,乳腺肿瘤中c-Myc mRNA表达增加。

结论

需要进一步开展大规模研究,以采用该实验性大鼠乳腺肿瘤模型作为体内模型,研究针对Myc或其转录或转录后水平下游靶点的抗癌策略。

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