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Association of the DNA methylation profile of the CYP1B1 gene with response to adjuvant therapy in breast cancer

机译:CYP1B1基因的DNA甲基化特征与乳腺癌辅助治疗的相关性

摘要

Particular embodiments provide novel and clinically useful DNA methylation predictors of hormone receptor status, and predictors of response to endocrine (e.g., hormonal) and non-endocrine breast cancer therapy. The ESR1 gene, encoding the estrogen receptor (ER) alpha proved to be the preferred predictor of progesterone receptor (PR) status, while methylation of the PGR gene, encoding PR, was the preferred predictor of ER status. ESR1 methylation outperformed hormone receptor status as a predictor of clinical response in patients treated with antiestroges (e.g., tamoxifen), while promoter methylation of the CYP1B1 gene, encoding a tamoxifen and estradiol metabolizing cytochrome P450, predicted response differentially in tamoxifen-treated and non-treated patients. High levels of promoter methylation of the ARH1 gene, encoding a RAS-related small G-protein, were shown to be preferred predictors of better survival in patients who had not received tamoxifen therapy.
机译:特定的实施方案提供了激素受体状态的新颖且临床上有用的DNA甲基化预测因子,以及对内分泌(例如激素)和非内分泌乳腺癌治疗反应的预测因子。编码雌激素受体(ER)α的ESR1基因被证明是孕激素受体(PR)状态的首选预测因子,而编码PR的PGR基因的甲基化是ER状态的优选预测因子。 ESR1甲基化优于激素受体状态作为抗雌激素(例如他莫昔芬)治疗患者临床反应的预测指标,而CYP1B1基因的启动子甲基化(编码他莫昔芬和雌二醇代谢细胞色素P450)则预测该反应在他莫昔芬治疗的患者和未治疗的非治疗的患者。研究表明,未接受他莫昔芬治疗的患者,ARH1基因的高水平启动子甲基化水平(编码与RAS有关的小G蛋白)是较好存活率的首选指标。

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