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2
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本文引用的文献

1
Oncogenic Ras and transforming growth factor-beta synergistically regulate AU-rich element-containing mRNAs during epithelial to mesenchymal transition.致癌性Ras与转化生长因子-β在上皮-间质转化过程中协同调节富含AU元件的mRNA。
Mol Cancer Res. 2008 Jul;6(7):1124-36. doi: 10.1158/1541-7786.MCR-07-2095.
2
Caveolin-1 in tumor progression: the good, the bad and the ugly.小窝蛋白-1在肿瘤进展中的作用:有利、有害与丑陋面
Cancer Metastasis Rev. 2008 Dec;27(4):715-35. doi: 10.1007/s10555-008-9160-9.
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Mice with cav-1 gene disruption have benign stromal lesions and compromised epithelial differentiation.
Exp Mol Pathol. 2008 Apr;84(2):131-40. doi: 10.1016/j.yexmp.2007.08.004. Epub 2007 Aug 31.
4
Active surveillance for early-stage prostate cancer: review of the current literature.早期前列腺癌的主动监测:当前文献综述
Cancer. 2008 Apr 15;112(8):1650-9. doi: 10.1002/cncr.23373.
5
Caveolin-1: a tumor-promoting role in human cancer.小窝蛋白-1:在人类癌症中发挥促癌作用。
Int J Radiat Biol. 2008 Mar;84(3):177-89. doi: 10.1080/09553000701745293.
6
Cancer statistics, 2008.2008年癌症统计数据。
CA Cancer J Clin. 2008 Mar-Apr;58(2):71-96. doi: 10.3322/CA.2007.0010. Epub 2008 Feb 20.
7
Tumor cell-secreted caveolin-1 has proangiogenic activities in prostate cancer.肿瘤细胞分泌的小窝蛋白-1在前列腺癌中具有促血管生成活性。
Cancer Res. 2008 Feb 1;68(3):731-9. doi: 10.1158/0008-5472.CAN-07-2668.
8
VEGF in biological control.生物控制中的血管内皮生长因子
J Cell Biochem. 2007 Dec 15;102(6):1358-67. doi: 10.1002/jcb.21579.
9
Caveolin-1 secreting LNCaP cells induce tumor growth of caveolin-1 negative LNCaP cells in vivo.分泌小窝蛋白-1的LNCaP细胞在体内诱导小窝蛋白-1阴性LNCaP细胞的肿瘤生长。
Int J Cancer. 2008 Feb 1;122(3):520-5. doi: 10.1002/ijc.23142.
10
Correlative evidence that prostate cancer cell-derived caveolin-1 mediates angiogenesis.前列腺癌细胞衍生的小窝蛋白-1介导血管生成的相关证据。
Hum Pathol. 2007 Nov;38(11):1688-95. doi: 10.1016/j.humpath.2007.03.024. Epub 2007 Aug 17.

窖蛋白-1 促进前列腺癌细胞的自调节、Akt 介导的致癌生长因子诱导。

Caveolin-1 promotes autoregulatory, Akt-mediated induction of cancer-promoting growth factors in prostate cancer cells.

机构信息

Department of Genitourinary Medical Oncology, University of Texas M D Anderson Cancer Center, Houston, TX 77030-4009, USA.

出版信息

Mol Cancer Res. 2009 Nov;7(11):1781-91. doi: 10.1158/1541-7786.MCR-09-0255. Epub 2009 Nov 10.

DOI:10.1158/1541-7786.MCR-09-0255
PMID:19903767
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3881562/
Abstract

Caveolin-1 (cav-1) and the cancer-promoting growth factors vascular endothelial growth factor (VEGF), transforming growth factor beta1 (TGF-beta1), and fibroblast growth factor 2 (FGF2) are often found to be upregulated in advanced prostate cancer and other malignancies. However, the relationship between cav-1 overexpression and growth factor upregulation remains unclear. This report presents, to our knowledge, the first evidence that in prostate cancer cells, a positive autoregulatory feedback loop is established in which VEGF, TGF-beta1, and FGF2 upregulate cav-1, and cav-1 expression, in turn, leads to increased levels of VEGF, TGF-beta1, and FGF2 mRNA and protein, resulting in enhanced invasive activities of prostate cancer cells, i.e., migration and motility. Our results further show that cav-1-enhanced mRNA stability is a major mechanism underlying the upregulation of these cancer-promoting growth factors, and that PI3-K-Akt signaling is required for forming this positive autoregulatory feedback loop.

摘要

窖蛋白-1(cav-1)和促进肿瘤生长的血管内皮生长因子(VEGF)、转化生长因子β1(TGF-β1)和成纤维细胞生长因子 2(FGF2)在晚期前列腺癌和其他恶性肿瘤中常被发现过度表达。然而,cav-1 过表达与生长因子上调之间的关系尚不清楚。本报告首次提出了在前列腺癌细胞中建立正反馈环的证据,即 VEGF、TGF-β1 和 FGF2 上调 cav-1,而 cav-1 表达又导致 VEGF、TGF-β1 和 FGF2 mRNA 和蛋白水平升高,从而增强了前列腺癌细胞的侵袭活性,即迁移和运动。我们的研究结果还表明,cav-1 增强的 mRNA 稳定性是上调这些促进癌症生长的生长因子的主要机制,而 PI3-K-Akt 信号通路是形成这种正反馈环所必需的。