Jeong Yangsik, Xie Yang, Lee Woochang, Bookout Angie L, Girard Luc, Raso Gabriela, Behrens Carmen, Wistuba Ignacio I, Gadzar Adi F, Minna John D, Mangelsdorf David J
Department of Biochemistry, Wonju College of Medicine, Yonsei University, Wonju, Gangwon-do 220-701, Republic of Korea.
Mol Endocrinol. 2012 Aug;26(8):1443-54. doi: 10.1210/me.2011-1382. Epub 2012 Jun 14.
Lung cancer is the leading cause of cancer-related death. Despite a number of studies that have provided prognostic biomarkers for lung cancer, a paucity of reliable markers and therapeutic targets exist to diagnose and treat this aggressive disease. In this study we investigated the potential of nuclear receptors (NRs), many of which are well-established drug targets, as therapeutic markers in lung cancer. Using quantitative real-time PCR, we analyzed the expression of the 48 members of the NR superfamily in a human panel of 55 normal and lung cancer cell lines. Unsupervised cluster analysis of the NR expression profile segregated normal from tumor cell lines and grouped lung cancers according to type (i.e. small vs. non-small cell lung cancers). Moreover, we found that the NR signature was 79% accurate in diagnosing lung cancer incidence in smokers (n = 129). Finally, the evaluation of a subset of NRs (androgen receptor, estrogen receptor, vitamin D receptor, and peroxisome proliferator-activated receptor-γ) demonstrated the therapeutic potential of using NR expression to predict ligand-dependent growth responses in individual lung cancer cells. Preclinical evaluation of one of these receptors (peroxisome proliferator activated receptor-γ) in mouse xenografts confirmed that ligand-dependent inhibitory growth responses in lung cancer can be predicted based on a tumor's receptor expression status. Taken together, this study establishes NRs as theragnostic markers for predicting lung cancer incidence and further strengthens their potential as therapeutic targets for individualized treatment.
肺癌是癌症相关死亡的主要原因。尽管已有多项研究提供了肺癌的预后生物标志物,但在诊断和治疗这种侵袭性疾病方面,可靠的标志物和治疗靶点仍然匮乏。在本研究中,我们调查了核受体(NRs)作为肺癌治疗标志物的潜力,其中许多核受体是公认的药物靶点。我们使用定量实时PCR分析了55种正常和肺癌细胞系的人类样本中NR超家族48个成员的表达。对NR表达谱进行无监督聚类分析,可区分正常细胞系和肿瘤细胞系,并根据类型(即小细胞肺癌与非小细胞肺癌)对肺癌进行分组。此外,我们发现NR特征在诊断吸烟者(n = 129)的肺癌发病率方面准确率为79%。最后,对一部分NRs(雄激素受体、雌激素受体、维生素D受体和过氧化物酶体增殖物激活受体-γ)的评估表明,利用NR表达预测个体肺癌细胞中配体依赖性生长反应具有治疗潜力。对其中一种受体(过氧化物酶体增殖物激活受体-γ)在小鼠异种移植模型中的临床前评估证实,基于肿瘤的受体表达状态可以预测肺癌中配体依赖性抑制生长反应。综上所述,本研究将NRs确立为预测肺癌发病率的治疗诊断标志物,并进一步强化了它们作为个体化治疗靶点的潜力。