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首页> 外文期刊>Molecular Carcinogenesis >Hedgehog signaling regulates drug sensitivity by targeting ABC transporters ABCB1 and ABCG2 in epithelial ovarian cancer
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Hedgehog signaling regulates drug sensitivity by targeting ABC transporters ABCB1 and ABCG2 in epithelial ovarian cancer

机译:刺猬信号通过靶向上皮性卵巢癌中的ABC转运蛋白ABCB1和ABCG2来调节药物敏感性

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A major challenge of successful chemotherapy in ovarian cancer is overcoming intrinsic or acquired multi-drug resistance caused by active drug efflux mediated by ATP-binding cassette (ABC) transporters. Regulation of these transporters in ovarian cancer is poorly understood. We have found that abnormal expression of the hedgehog (Hh) signaling pathway transcription factor Gli1 is involved in the regulation of ABC transporters ABCB1 and ABCG2 in ovarian cancer. Hh is a known regulator of cancer cell proliferation and differentiation in several other types of invasive and metastatic malignancies. Our work has demonstrated that Gli1 is abnormally activated in a portion of ovarian cancers. Inhibition of Gli1 expression decreases ABCB1 and ABCG2 gene expression levels and enhances the response of ovarian cancer cells to certain chemotherapeutic drugs. The underlying mechanism is a direct association of Gli1 with a specific consensus sequence located in the promoter region of ABCB1 and ABCG2 genes. This study provides new understanding of ABC gene regulation by Hh signaling pathway, which may lead to the identification of new markers to detect and to anticipate ovarian cancer chemotherapy drug sensitivity.
机译:卵巢癌成功化疗的主要挑战是克服由ATP结合盒(ABC)转运蛋白介导的活性药物外流引起的内在或获得性多药耐药性。这些转运蛋白在卵巢癌中的调控知之甚少。我们已经发现,刺猬(Hh)信号通路转录因子Gli1的异常表达参与卵巢癌中ABC转运蛋白ABCB1和ABCG2的调节。 Hh是几种其他类型的浸润性和转移性恶性肿瘤中癌细胞增殖和分化的已知调节剂。我们的工作表明,Gli1在部分卵巢癌中被异常激活。抑制Gli1表达可降低ABCB1和ABCG2基因表达水平,并增强卵巢癌细胞对某些化疗药物的反应。潜在的机制是Gli1与位于ABCB1和ABCG2基因启动子区域的特定共有序列的直接关联。这项研究提供了新的认识,通过Hh信号通路调节ABC基因,这可能导致鉴定新的标志物,以检测和预期卵巢癌化疗药物的敏感性。

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