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Reversible inhibition of lysine specific demethylase 1 is a novel anti-tumor strategy for poorly differentiated endometrial carcinoma

机译:可逆抑制赖氨酸特异性脱甲基酶1是低分化子宫内膜癌的新型抗肿瘤策略

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摘要

BackgroundEndometrial cancer is the most common gynecologic malignancy. Type II endometrial carcinoma is often poorly differentiated and patients diagnosed with Type II disease (~11%) are disproportionately represented in annual endometrial cancer deaths (48%). Recent genomic studies highlight mutations in chromatin regulators as drivers in Type II endometrial carcinoma tumorigenesis, suggesting the use of epigenetic targeted therapies could provide clinical benefit to these patients. We investigated the anti-tumor efficacy of the LSD1 inhibitor HCI2509 in two poorly differentiated Type II endometrial cancer cell lines AN3CA and KLE.
机译:背景子宫内膜癌是最常见的妇科恶性肿瘤。 II型子宫内膜癌通常很难区分,诊断为II型疾病的患者(〜11%)在每年的子宫内膜癌死亡人数中所占比例不成比例(48%)。最近的基因组研究突出了染色质调节剂中的突变作为II型子宫内膜癌肿瘤发生的驱动因素,表明表观遗传靶向疗法的使用可能为这些患者提供临床益处。我们研究了LSD1抑制剂HCI2509在两种低分化II型子宫内膜癌细胞系AN3CA和KLE中的抗肿瘤功效。

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