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肥胖会增强致癌物7,12-二甲基苯并[a]蒽在体外和体内诱导的肿瘤发生。

Obesity enhances carcinogen 7, 12-Dimethylbenz [a] anthracene -induced tumorigenesis in vitro and in vivo.

作者信息

Hsieh Chia-Chien, Peng Shih-Han, Chou Mei-Jia

机构信息

Department of Human Development and Family Studies (Nutritional Science & Education), National Taiwan Normal University, No. 162, Heping East Road, Section 1, Taipei 10610, Taiwan.

出版信息

Food Chem Toxicol. 2017 Dec;110:156-164. doi: 10.1016/j.fct.2017.10.024. Epub 2017 Oct 16.

DOI:10.1016/j.fct.2017.10.024
PMID:29042292
Abstract

Growing body of evidence shows that extra adiposity influences on the progression of multiple cancers, including breast cancer. The aim of this study is to investigate whether obesity correlates with mammary tumor development in vitro and in vivo. We found that obesity-related mediators, 3T3-L1 adipocyte conditioned medium, enhanced formation of cancerous foci induced by the carcinogen 7,12-Dimethylbenz[a]anthracene (DMBA) in NIH/3T3 fibroblasts, in vitro. Additionally, we tested the effect of obesity in mouse model of DMBA-induced breast cancer. C57BL/6J female mice were fed a low fat (LF), or high fat (HF) diet, and DMBA was administered by oral gavage (LF plus DMBA [LFD] and HF plus DMBA [HFD]). Our results indicated that HFD mouse developed a tumor which weight was 169mg, whereas the LFD mouse developed a tumor weight of 77mg. Histological analysis of the mammary tumor from HFD group showed morphological aggressiveness and multiple cell type infiltration compared to LFD group. The epididymal adipose tissue from the DMBA groups showed more macrophage infiltration, polarized towards an M1 phenotype compared to the non-DMBA mice. HF mice showed less accumulation of M2 macrophages in the adipose tissue. In summary, obese mediators enhanced DMBA induced tumorigenesis in vitro and in vivo.

摘要

越来越多的证据表明,额外的肥胖会影响多种癌症的进展,包括乳腺癌。本研究的目的是调查肥胖是否与体外和体内的乳腺肿瘤发展相关。我们发现,肥胖相关介质,即3T3-L1脂肪细胞条件培养基,在体外可增强致癌物7,12-二甲基苯并[a]蒽(DMBA)诱导的NIH/3T3成纤维细胞癌灶的形成。此外,我们在DMBA诱导的乳腺癌小鼠模型中测试了肥胖的影响。给C57BL/6J雌性小鼠喂食低脂(LF)或高脂(HF)饮食,并通过口服灌胃给予DMBA(LF加DMBA [LFD]和HF加DMBA [HFD])。我们的结果表明,HFD组小鼠的肿瘤重量为169mg,而LFD组小鼠的肿瘤重量为77mg。与LFD组相比,HFD组乳腺肿瘤的组织学分析显示出形态学侵袭性和多种细胞类型浸润。与未接受DMBA的小鼠相比,DMBA组的附睾脂肪组织显示出更多的巨噬细胞浸润,且向M1表型极化。HF小鼠的脂肪组织中M2巨噬细胞的积累较少。总之,肥胖介质在体外和体内均增强了DMBA诱导的肿瘤发生。

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