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赖氨酸特异性去甲基化酶1(LSD1)抑制剂在肺癌中的抗肿瘤活性

Antitumor activity of LSD1 inhibitors in lung cancer.

作者信息

Mohammad Helai P, Kruger Ryan G

机构信息

Cancer Epigenetics, GlaxoSmithKline , Collegeville, PA, USA.

出版信息

Mol Cell Oncol. 2016 Jan 6;3(2):e1117700. doi: 10.1080/23723556.2015.1117700. eCollection 2016 Mar.

Abstract

Epigenetic machinery have become a major focus for new targeted cancer therapies. Our previous report described the discovery and biological activity of a potent, selective, orally bioavailable, irreversible inhibitor of Lysine Demethylase 1 (LSD1), GSK2879552. A proliferation screen of cell lines representing a number of tumor types indicated that small cell lung carcinoma (SCLC) was sensitive to LSD1 inhibition. The SCLC lines that undergo growth inhibition in response to GSK2879552 exhibit DNA hypomethylation of a signature set of probes suggesting this may be used as a predictive biomarker of activity. This targeted mechanism coupled with a novel predictive biomarker make LSD1 inhibition an exciting potential therapy for SCLC.

摘要

表观遗传机制已成为新型靶向癌症治疗的主要焦点。我们之前的报告描述了赖氨酸去甲基化酶1(LSD1)的一种强效、选择性、口服生物可利用的不可逆抑制剂GSK2879552的发现及其生物学活性。对代表多种肿瘤类型的细胞系进行的增殖筛选表明,小细胞肺癌(SCLC)对LSD1抑制敏感。响应GSK2879552而发生生长抑制的SCLC细胞系表现出一组特征性探针的DNA低甲基化,这表明这可作为活性的预测生物标志物。这种靶向机制与一种新型预测生物标志物相结合,使得LSD1抑制成为SCLC一种令人兴奋的潜在治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d8e/4905412/8a7a1b332409/kmco-03-02-1117700-g001.jpg

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