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胰岛素样生长因子-I先天性缺乏的患者似乎对恶性肿瘤的发生具有抵抗力:初步报告。

Patients with congenital deficiency of IGF-I seem protected from the development of malignancies: a preliminary report.

作者信息

Shevah O, Laron Z

机构信息

Endocrinology and Diabetes Research Unit, Schneider Children's Medical Center, 14 Kaplan Street, Petah-Tikva 49202, Israel.

出版信息

Growth Horm IGF Res. 2007 Feb;17(1):54-7. doi: 10.1016/j.ghir.2006.10.007. Epub 2006 Dec 12.

DOI:10.1016/j.ghir.2006.10.007
PMID:17166755
Abstract

OBJECTIVE

Overexpression of IGF-I occurs in tumors diagnosed in childhood (osteosarcoma, Wilms tumor, neuroblastoma, etc.) and in adults (breast, ovaries, colon and prostate cancer). The aim of our study was to establish the prevalence of malignancies in states of congenital IGF-I deficiency.

SUBJECTS

We surveyed 222 patients with congenital IGF-I deficiency (Laron syndrome, GH gene deletion, GHRH receptor defects and IGF-I resistance) and 338 first and second-degree relatives.

RESULTS

None of the IGF-I deficient patients had cancer, whereas 9-24% of the family members had a history of malignancy.

CONCLUSIONS

Congenital IGF-I deficiency acts as a protecting factor for the development of cancer.

摘要

目的

胰岛素样生长因子-I(IGF-I)过表达出现在儿童期诊断出的肿瘤(骨肉瘤、肾母细胞瘤、神经母细胞瘤等)以及成人肿瘤(乳腺癌、卵巢癌、结肠癌和前列腺癌)中。我们研究的目的是确定先天性IGF-I缺乏状态下恶性肿瘤的患病率。

对象

我们调查了222例先天性IGF-I缺乏患者(拉伦综合征、生长激素基因缺失、生长激素释放激素受体缺陷和IGF-I抵抗)以及338名一级和二级亲属。

结果

IGF-I缺乏患者中无人患癌症,而9%-24%的家庭成员有恶性肿瘤病史。

结论

先天性IGF-I缺乏是癌症发生发展的保护因素。

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