Chromatin-associated CSF-1R binds to the promoter of proliferation-related genes in breast cancer cells

被引:31
作者
Barbetti, V. [1 ]
Morandi, A. [1 ]
Tusa, I. [1 ]
Digiacomo, G. [1 ]
Riverso, M. [1 ]
Marzi, I. [1 ]
Cipolleschi, M. G. [1 ]
Bessi, S. [2 ]
Giannini, A. [2 ]
Di Leo, A. [3 ]
Dello Sbarba, P. [1 ]
Rovida, E. [1 ]
机构
[1] Univ Florence, Sez Patol, Dipartimento Sci Biomed Sperimentali & Clin, Ist Toscano Tumori, I-50134 Florence, Italy
[2] Osped Prato, Prato, Italy
[3] Hosp Prato, Ist Toscano Tumori, Dept Oncol, Sandro Pitigliani Med Oncol Unit, Prato, Italy
关键词
CSF-1; nuclear proteins; breast cancer; Fms; nuclear receptor tyrosine kinase; COLONY-STIMULATING FACTOR; FIBROBLAST-GROWTH-FACTOR; FACTOR-I; NUCLEAR TRANSLOCATION; FACTOR-RECEPTOR; C-FMS; MACROPHAGE PRODUCTION; SIGNAL-TRANSDUCTION; TYROSINE KINASE; CERVICAL-CANCER;
D O I
10.1038/onc.2013.542
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The colony-stimulating factor-1 (CSF-1) and its receptor CSF-1R physiologically regulate the monocyte/macrophage system, trophoblast implantation and breast development. An abnormal CSF-1R expression has been documented in several human epithelial tumors, including breast carcinomas. We recently demonstrated that CSF-1/CSF-1R signaling drives proliferation of breast cancer cells via 'classical' receptor tyrosine kinase signaling, including activation of the extracellular signal-regulated kinase 1/2. In this paper, we show that CSF-1R can also localize within the nucleus of breast cancer cells, either cell lines or tissue specimens, irrespectively of their intrinsic molecular subtype. We found that the majority of nuclear CSF-1R is located in the chromatin-bound subcellular compartment. Chromatin immunoprecipitation revealed that CSF-1R, once in the nucleus, binds to the promoters of the proliferation-related genes CCND1, c-JUN and c-MYC. CSF-1R also binds the promoter of its ligand CSF-1 and positively regulates CSF-1 expression. The existence of such a receptor/ligand regulatory loop is a novel aspect of CSF-1R signaling. Moreover, our results provided the first evidence of a novel localization site of CSF-1R in breast cancer cells, suggesting that CSF-1R could act as a transcriptional regulator on proliferation-related genes.
引用
收藏
页码:4359 / 4364
页数:6
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