Department of Clinical Cancer Prevention, The University of Texas M D Anderson Cancer Center, Houston, TX 77030, USA.
Breast Cancer Res Treat. 2012 Jun;133(2):487-500. doi: 10.1007/s10549-011-1775-9. Epub 2011 Sep 24.
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.
转染/甲状腺乳头状癌(RET/PTC)酪氨酸激酶重排是一种癌基因,参与甲状腺癌的发生。我们和其他人最近的研究表明,雌激素可诱导乳腺癌细胞中 RET/PTC 激酶的表达。由于雌激素调节基因在乳腺癌发病机制中的关键作用,我们研究了 RET/PTC 激酶在乳腺癌细胞中的表达、调控和功能。我们发现,RET/PTC 激酶的表达与乳腺癌细胞和肿瘤标本中的雌激素受体(ER)表达相关,并且在 ER 阳性乳腺癌患者中,RET/PTC 激酶的表达与预后不良相关。我们发现,雌激素可快速诱导乳腺癌细胞中 RET/PTC 激酶的表达,且这种诱导是通过转录调控机制进行的。通过报告基因分析、小干扰 RNA(siRNA)分析和染色质免疫沉淀(ChIP)分析,我们证明了 ER 和叉头框 A1(FOXA1)转录因子之间的相互作用在调节 RET/PTC 激酶表达中的必要性。在功能研究中,雌激素刺激引起的 RET/PTC 激酶表达增加导致多个下游激酶信号通路的磷酸化水平升高。相反,RET/PTC 表达的下调与这些相同的激酶信号通路的抑制有关,实际上,还降低了雌激素对 ER 阳性乳腺癌细胞增殖的刺激作用。这些结果表明 ER 和 FOXA1 转录因子相互作用在调节 RET/PTC 激酶表达中的一条新途径,并表明 RET/PTC 激酶是 ER 阳性乳腺癌细胞增殖的关键调节因子。综上所述,我们的研究表明,RET/PTC 激酶可能是 ER 阳性乳腺癌的一种新的预后生物标志物和治疗靶点,可用于预防和治疗该疾病。