Molecular Mechanisms Unit, Department of Experimental Oncology and Molecular Medicine, IRCCS Foundation--Istituto Nazionale dei Tumori, Milan, Italy.
Oncogene. 2010 Jul 1;29(26):3835-44. doi: 10.1038/onc.2010.136. Epub 2010 May 3.
Insulin-like growth factor-binding protein 7 (IGFBP7) is a secreted protein involved in several cellular processes, including proliferation, senescence and apoptosis. Loss of IGFBP7 expression is a critical step in the development of human tumors, including melanoma and colon cancer. By microarray gene expression studies, we have detected downregulation of IGFBP7 gene expression in follicular and papillary thyroid tumors in comparison with normal thyroid tissue. Evaluation of publicly available PTC microarray gene expression data sets confirmed, in a consistent fraction of tumors, the downregulation of IGFBP7 transcript levels. The functional consequence of IGFBP7 downregulation was addressed in the PTC-derived NIM1 cell line in which IGFBP7 expression is repressed by promoter hypermethylation. Exposure to soluble IGFBP7 protein or restoration of IGFBP7 expression by complementary DNA transfection reduced growth rate, migration, anchorage-independent growth and tumorigenicity of NIM1 cells. We show that the effects of IGFBP7 are related to apoptosis. Our data suggest that loss of IGFBP7 expression has a functional role in thyroid carcinogenesis, and it may represent a possible basis for therapeutic strategies.
胰岛素样生长因子结合蛋白 7(IGFBP7)是一种分泌蛋白,参与多种细胞过程,包括增殖、衰老和凋亡。IGFBP7 表达的缺失是人类肿瘤(包括黑色素瘤和结肠癌)发展的关键步骤。通过微阵列基因表达研究,我们发现与正常甲状腺组织相比,滤泡性和乳头状甲状腺肿瘤中 IGFBP7 基因表达下调。对公开可用的 PTC 微阵列基因表达数据集的评估在肿瘤的一致部分中证实了 IGFBP7 转录本水平的下调。在 PTC 衍生的 NIM1 细胞系中,通过启动子超甲基化抑制 IGFBP7 的表达,研究了 IGFBP7 下调的功能后果。暴露于可溶性 IGFBP7 蛋白或通过 cDNA 转染恢复 IGFBP7 表达可降低 NIM1 细胞的生长速度、迁移、无锚定生长和致瘤性。我们表明 IGFBP7 的作用与细胞凋亡有关。我们的数据表明,IGFBP7 表达的缺失在甲状腺癌发生中具有功能作用,它可能代表一种潜在的治疗策略基础。