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绝经后乳腺癌患者超重的分子意义,与胰岛素样生长因子I受体和胰岛素样生长因子II基因表达的关系

Molecular significance of excess body weight in postmenopausal breast cancer patients, in relation to expression of insulin-like growth factor I receptor and insulin-like growth factor II genes.

作者信息

Suga K, Imai K, Eguchi H, Hayashi S, Higashi Y, Nakachi K

机构信息

Department of Transfusion Medicine, Saga Medical School Hospital, Saga 849-8501, Japan.

出版信息

Jpn J Cancer Res. 2001 Feb;92(2):127-34. doi: 10.1111/j.1349-7006.2001.tb01074.x.

DOI:10.1111/j.1349-7006.2001.tb01074.x
PMID:11223541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5926695/
Abstract

A number of epidemiological and clinical studies have revealed that excess body weight increases the risk of postmenopausal breast cancer and also adversely affects subsequent malignant progression. To elucidate the molecular mechanisms underlying these observations, we examined mRNA expression of various genes in normal (non-cancerous) mammary gland and cancer tissue of Japanese patients with primary breast cancer, in association with their body mass index (BMI). On the basis of analysis of 106 breast cancer patients, we found that mRNA expression of insulin-like growth factor I receptor (IGF-IR) and insulin-like growth factor II (IGF-II) in the normal mammary gland showed a significant and positive association with increased BMI among postmenopausal patients. Furthermore, the positive association of increased BMI with IGF-IR mRNA expression was also found in postmenopausal breast cancer tissue, while this association was not observed among premenopausal patients. In addition, increased mRNA expression of cyclin D1 and bcl-2 was observed in association with increased mRNA levels of IGF-IR among the patients regardless of menopausal status. These findings suggest that the molecular consequence of the increased BMI is the increased expression of IGF-II and IGF-IR, resulting in development of postmenopausal breast cancer and its progression mediated through modulation of the cell cycle and apoptosis.

摘要

多项流行病学和临床研究表明,超重会增加绝经后乳腺癌的风险,并且还会对后续的恶性进展产生不利影响。为了阐明这些观察结果背后的分子机制,我们检测了日本原发性乳腺癌患者正常(非癌性)乳腺组织和癌组织中各种基因的mRNA表达,并将其与体重指数(BMI)相关联。基于对106例乳腺癌患者的分析,我们发现,在绝经后患者中,正常乳腺组织中胰岛素样生长因子I受体(IGF-IR)和胰岛素样生长因子II(IGF-II)的mRNA表达与BMI升高呈显著正相关。此外,在绝经后乳腺癌组织中也发现BMI升高与IGF-IR mRNA表达呈正相关,而在绝经前患者中未观察到这种关联。此外,无论绝经状态如何,患者中细胞周期蛋白D1和bcl-2的mRNA表达增加与IGF-IR的mRNA水平升高相关。这些发现表明,BMI升高的分子后果是IGF-II和IGF-IR表达增加,导致绝经后乳腺癌的发生及其通过调节细胞周期和凋亡介导的进展。