The rearranged during transfection/papillary thyroid carcinoma tyrosine kinase is an estrogen-dependent gene required for the growth of estrogen receptor positive breast cancer cells

被引:0
|
作者
Chunyu Wang
Julie Ann Mayer
Abhijit Mazumdar
Powel H. Brown
机构
[1] The University of Texas M. D. Anderson Cancer Center,Department of Clinical Cancer Prevention
来源
Breast Cancer Research and Treatment | 2012年 / 133卷
关键词
Estrogen; Breast cancer; Rearranged during transfection; Papillary thyroid carcinoma; Kinase; Transcription factor crosstalk;
D O I
暂无
中图分类号
学科分类号
摘要
The rearranged during transfection/papillary thyroid carcinoma (RET/PTC) tyrosine kinase is an oncogene implicated in the tumorigenesis of thyroid cancer. Recent studies by us and others have shown that RET/PTC kinase expression is induced by estrogen in breast cancer cells. Due to the critical involvement of estrogen-regulated genes in the pathogenesis of breast cancer, we investigated the expression, regulation, and function of RET/PTC kinase in breast cancer cells. We found that RET/PTC kinase expression correlates with estrogen receptor (ER) expression in breast cancer cells and tumor specimens, and that RET/PTC kinase expression is associated with a poor prognosis in ER-positive breast cancer patients. We found that estrogen rapidly induces RET/PTC kinase expression in an ER-dependent manner in breast cancer cells and that this induction is through a transcriptional regulatory mechanism. Using reporter assays, small interfering RNA (siRNA) assays, and chromatin immunoprecipitation (ChIP) assays, we demonstrated the necessity of crosstalk between ER and the forkhead box A1 (FOXA1) transcription factor in regulating RET/PTC kinase expression. In functional studies, increased expression of RET/PTC kinase induced by estrogen stimulation resulted in elevated phosphorylation of multiple downstream kinase signaling pathways. Conversely, knockdown of RET/PTC expression was associated with the inhibition of these same kinase signaling pathways, and, in fact, decreased the stimulatory effect of estrogen on the proliferation of ER-positive breast cancer cells. These results demonstrate a novel pathway of ER and FOXA1 transcription factor crosstalk in regulating RET/PTC kinase expression, and demonstrate that RET/PTC kinase is a critical regulator for the proliferation of ER-positive breast cancer cells. Taken together, our study suggests that RET/PTC kinase may serve as a novel prognostic biomarker and therapeutic target for prevention and treatment of ER-positive breast cancer.
引用
收藏
页码:487 / 500
页数:13
相关论文
共 50 条
  • [41] Estrogen regulation of vascular endothelial growth factor gene expression in ZR-75 breast cancer cells through interaction of estrogen receptor α and SP proteins
    Stoner, M
    Wormke, M
    Saville, B
    Samudio, I
    Qin, CH
    Abdelrahim, M
    Safe, S
    ONCOGENE, 2004, 23 (05) : 1052 - 1063
  • [42] Estrogen regulation of vascular endothelial growth factor gene expression in ZR-75 breast cancer cells through interaction of estrogen receptor α and SP proteins
    Matthew Stoner
    Mark Wormke
    Brad Saville
    Ismael Samudio
    Chunhua Qin
    Maen Abdelrahim
    Stephen Safe
    Oncogene, 2004, 23 : 1052 - 1063
  • [43] Effects of diverse dietary phytoestrogens on cell growth, cell cycle and apoptosis in estrogen-receptor-positive breast cancer cells
    Sakamoto, Takako
    Horiguchi, Hyogo
    Oguma, Etsuko
    Kayama, Fujio
    JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2010, 21 (09) : 856 - 864
  • [44] The aromatase inhibitor letrozole and inhibitors of insulin-like growth factor I receptor synergistically induce apoptosis in in vitro models of estrogen-dependent breast cancer
    Joanna Lisztwan
    Astrid Pornon
    Bin Chen
    Shiuan Chen
    Dean B Evans
    Breast Cancer Research, 10
  • [45] Concentration-dependent mitogenic and antiproliferative actions of 2-methoxyestradiol in estrogen receptor-positive human breast cancer cells
    Liu, ZJ
    Zhu, BT
    JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2004, 88 (03) : 265 - 275
  • [46] Influence of the Length and Positioning of the Antiestrogenic Side Chain of Endoxifen and 4-Hydroxytamoxifen on Gene Activation and Growth of Estrogen Receptor Positive Cancer Cells
    Maximov, Philipp Y.
    Fernandes, Daphne J.
    McDaniel, Russell E.
    Myers, Cynthia B.
    Curpan, Ramona F.
    Jordan, V. Craig
    JOURNAL OF MEDICINAL CHEMISTRY, 2014, 57 (11) : 4569 - 4583
  • [47] UBE2C Overexpression Aggravates Patient Outcome by Promoting Estrogen-Dependent/Independent Cell Proliferation in Early Hormone Receptor-Positive and HER2-Negative Breast Cancer
    Kim, Yu-Jin
    Lee, Gyunghwa
    Han, Jinil
    Song, Kyoung
    Choi, Joon-Seok
    Choi, Yoon-La
    Shin, Young Kee
    FRONTIERS IN ONCOLOGY, 2020, 9
  • [49] Estrogen receptor α mediated induction of the transforming growth factor α gene by estradiol and 4-hydroxytamoxifen in MDA-MB-231 breast cancer cells
    Schafer, JM
    Liu, H
    Levenson, AS
    Horiguchi, J
    Chen, ZH
    Jordan, C
    JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2001, 78 (01) : 41 - 50
  • [50] Formononetin-induced Apoptosis by Activation of Ras/p38 Mitogen-activated Protein Kinase in Estrogen Receptor-positive Human Breast Cancer Cells
    Chen, J.
    Sun, L.
    HORMONE AND METABOLIC RESEARCH, 2012, 44 (13) : 943 - 948