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核受体与受体酪氨酸激酶抑制剂联合治疗肺癌的潜力。

Combined therapeutic potential of nuclear receptors with receptor tyrosine kinase inhibitors in lung cancer.

机构信息

Department of Biochemistry, Wonju College of Medicine, Yonsei University, Wonju, Gangwon-do 220-701, Republic of Korea; Institute of Lifestyle Medicine, Wonju College of Medicine, Yonsei University, Wonju, Gangwon-do 220-701, Republic of Korea; Nuclear Receptor Research Consortium, Wonju College of Medicine, Yonsei University, Wonju, Gangwon-do 220-701, Republic of Korea.

Department of Pathology, Wonju College of Medicine, Yonsei University, Wonju, Gangwon-do 220-701, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2014 May 9;447(3):490-5. doi: 10.1016/j.bbrc.2014.04.018. Epub 2014 Apr 13.

DOI:10.1016/j.bbrc.2014.04.018
PMID:24735536
Abstract

Cancer heterogeneity is a big hurdle in achieving complete cancer treatment, which has led to the emergence of combinational therapy. In this study, we investigated the potential use of nuclear receptor (NR) ligands for combinational therapy with other anti-cancer drugs. We first profiled all 48 NRs and 48 biological anti-cancer targets in four pairs of lung cell lines, where each pair was obtained from the same patient. Two sets of cell lines were normal and the corresponding tumor cell lines while the other two sets consisted of primary versus metastatic tumor cell lines. Analysis of the expression profile revealed 11 NRs and 15 cancer targets from the two pairs of normal versus tumor cell lines, and 9 NRs and 9 cancer targets from the primary versus metastatic tumor cell lines had distinct expression patterns in each category. Finally, the evaluation of nuclear receptor ligand T0901317 for liver X receptor (LXR) demonstrated its combined therapeutic potential with tyrosine kinase inhibitors. The combined treatment of cMET inhibitor PHA665752 or EGFR inhibitor gefitinib with T0901317 showed additive growth inhibition in both H2073 and H1993 cells. Mechanistically, the combined treatment suppressed cell cycle progression by inhibiting cyclinD1 and cyclinB expression. Taken together, this study provides insight into the potential use of NR ligands in combined therapeutics with other biological anti-cancer drugs.

摘要

癌症异质性是实现完全癌症治疗的一大障碍,这导致了联合治疗的出现。在这项研究中,我们研究了核受体 (NR) 配体与其他抗癌药物联合治疗的潜力。我们首先对来自同一患者的四对肺细胞系中的 48 个 NR 和 48 个生物抗癌靶点进行了分析。两组细胞系为正常细胞系和相应的肿瘤细胞系,而另外两组细胞系由原发性肿瘤细胞系和转移性肿瘤细胞系组成。表达谱分析显示,来自正常细胞系与肿瘤细胞系的两对细胞系中有 11 个 NR 和 15 个癌症靶点,而来自原发性肿瘤细胞系与转移性肿瘤细胞系的 9 个 NR 和 9 个癌症靶点在每个类别中都有明显的表达模式。最后,对核受体配体 T0901317 进行了肝 X 受体 (LXR) 的评估,证明了其与酪氨酸激酶抑制剂联合治疗的潜力。cMET 抑制剂 PHA665752 或 EGFR 抑制剂吉非替尼与 T0901317 的联合治疗在 H2073 和 H1993 细胞中均显示出相加的生长抑制作用。从机制上讲,联合治疗通过抑制细胞周期蛋白 D1 和细胞周期蛋白 B 的表达来抑制细胞周期进程。总之,这项研究为 NR 配体与其他生物抗癌药物联合治疗提供了新的思路。

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