人类生长激素调节的HOXA1是一种人类乳腺上皮癌基因。
Human growth hormone-regulated HOXA1 is a human mammary epithelial oncogene.
作者信息
Zhang Xin, Zhu Tao, Chen Yong, Mertani Hichem C, Lee Kok-Onn, Lobie Peter E
机构信息
Institute of Molecular and Cell Biology and Department of Medicine, National University of Singapore, 30 Medical Dr., Singapore 117609, Republic of Singapore.
出版信息
J Biol Chem. 2003 Feb 28;278(9):7580-90. doi: 10.1074/jbc.M212050200. Epub 2002 Dec 13.
Increased mammary epithelial expression of the human growth hormone (hGH) gene is associated with the acquisition of pathological proliferation. We report here that autocrine hGH production by human mammary carcinoma cells increased the expression and transcriptional activity of the homeobox domain containing protein HOXA1. Forced expression of HOXA1 in human mammary carcinoma cells resulted in increased total cell number primarily by the promotion of cell survival mediated by the transcriptional up-regulation of Bcl-2. HOXA1 also abrogated the apoptotic response of mammary carcinoma cells to doxorubicin. Forced expression of HOXA1 in mammary carcinoma cells, in a Bcl-2-dependent manner, resulted in dramatic enhancement of anchorage-independent proliferation and colony formation in soft agar. Finally, forced expression of HOXA1 was sufficient to result in the oncogenic transformation of immortalized human mammary epithelial cells with aggressive in vivo tumor formation. Herein, we have therefore provided a molecular mechanism by which autocrine hGH stimulation of human mammary epithelial cells may result in oncogenic transformation.
人类生长激素(hGH)基因在乳腺上皮中的表达增加与病理性增殖的发生有关。我们在此报告,人乳腺癌细胞自分泌hGH可增加含同源异型框结构域蛋白HOXA1的表达及转录活性。在人乳腺癌细胞中强制表达HOXA1主要通过促进由Bcl-2转录上调介导的细胞存活,导致细胞总数增加。HOXA1还消除了乳腺癌细胞对阿霉素的凋亡反应。在乳腺癌细胞中以Bcl-2依赖的方式强制表达HOXA1,导致软琼脂中锚定非依赖性增殖和集落形成显著增强。最后,强制表达HOXA1足以导致永生化人乳腺上皮细胞发生致癌转化,并在体内形成侵袭性肿瘤。因此,我们在此提供了一种分子机制,通过该机制人乳腺上皮细胞的自分泌hGH刺激可能导致致癌转化。