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

被引:30
|
作者
Suga, K
Imai, K
Eguchi, H
Hayashi, S
Higashi, Y
Nakachi, K
机构
[1] Saga Med Sch Hosp, Dept Transfus Med, Saga 8498501, Japan
[2] Saitama Canc Ctr, Res Inst, Ina, Saitama 3620806, Japan
[3] Saitama Canc Ctr Hosp, Ina, Saitama 3620806, Japan
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 2001年 / 92卷 / 02期
关键词
breast cancer; body mass index; insulin-like growth factor II; insulin-like growth factor I receptor;
D O I
10.1111/j.1349-7006.2001.tb01074.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 (BR II). 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 fatter II (IGF-ZI) 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 BR-II 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.
引用
收藏
页码:127 / 134
页数:8
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