Centre for Metabolism, Obesity and Diabetes Research, McMaster University, Hamilton, Canada.
Centre for Discovery in Cancer Research, McMaster University, Hamilton, Canada.
Mol Oncol. 2023 Nov;17(11):2235-2256. doi: 10.1002/1878-0261.13508. Epub 2023 Aug 27.
Non-small cell lung cancer (NSCLC) has a poor prognosis, and effective therapeutic strategies are lacking. The diabetes drug canagliflozin inhibits NSCLC cell proliferation and the mammalian target of rapamycin (mTOR) pathway, which mediates cell growth and survival, but it is unclear whether this drug can enhance response rates when combined with cytotoxic therapy. Here, we evaluated the effects of canagliflozin on human NSCLC response to cytotoxic therapy in tissue cultures and xenografts. Ribonucleic acid sequencing (RNA-seq), real-time quantitative PCR (RT-qPCR), metabolic function, small interfering ribonucleic acid (siRNA) knockdown, and protein expression assays were used in mechanistic analyses. We found that canagliflozin inhibited proliferation and clonogenic survival of NSCLC cells and augmented the efficacy of radiotherapy to mediate these effects and inhibit NSCLC xenograft growth. Canagliflozin treatment alone moderately inhibited mitochondrial oxidative phosphorylation and exhibited greater antiproliferative capacity than specific mitochondrial complex-I inhibitors. The treatment downregulated genes mediating hypoxia-inducible factor (HIF)-1α stability, metabolism and survival, activated adenosine monophosphate-activated protein kinase (AMPK) and inhibited mTOR, a critical activator of hypoxia-inducible factor-1α (HIF-1α) signaling. HIF-1α knockdown and stabilization experiments suggested that canagliflozin mediates antiproliferative effects, in part, through suppression of HIF-1α. Transcriptional regulatory network analysis pinpointed histone deacetylase 2 (HDAC2), a gene suppressed by canagliflozin, as a key mediator of canagliflozin's transcriptional reprogramming. HDAC2 knockdown eliminated HIF-1α levels and enhanced the antiproliferative effects of canagliflozin. HDAC2-regulated genes suppressed by canagliflozin are associated with poor prognosis in several clinical NSCLC datasets. In addition, we include evidence that canagliflozin also improves NSCLC response to chemotherapy. In summary, canagliflozin may be a promising therapy to develop in combination with cytotoxic therapy in NSCLC.
非小细胞肺癌(NSCLC)预后较差,缺乏有效的治疗策略。糖尿病药物卡格列净可抑制非小细胞肺癌细胞增殖和哺乳动物雷帕霉素靶蛋白(mTOR)通路,该通路介导细胞生长和存活,但尚不清楚该药物与细胞毒性疗法联合使用是否能提高反应率。在这里,我们评估了卡格列净对组织培养和异种移植中人类 NSCLC 对细胞毒性治疗的反应的影响。使用核糖核酸测序(RNA-seq)、实时定量 PCR(RT-qPCR)、代谢功能、小干扰核糖核酸(siRNA)敲低和蛋白表达分析进行机制分析。我们发现卡格列净抑制 NSCLC 细胞的增殖和集落形成存活,并增强放射治疗的疗效,以介导这些效应并抑制 NSCLC 异种移植的生长。卡格列净单独治疗可适度抑制线粒体氧化磷酸化,并表现出比特异性线粒体复合物-I 抑制剂更强的抗增殖能力。该治疗下调了介导缺氧诱导因子(HIF)-1α稳定性、代谢和存活的基因,激活了腺苷单磷酸激活蛋白激酶(AMPK)并抑制了 mTOR,后者是缺氧诱导因子-1α(HIF-1α)信号的关键激活剂。HIF-1α 敲低和稳定实验表明,卡格列净通过抑制 HIF-1α介导抗增殖作用。转录调控网络分析确定了组蛋白去乙酰化酶 2(HDAC2),即卡格列净抑制的基因,作为卡格列净转录重编程的关键介质。HDAC2 敲低消除了 HIF-1α 水平并增强了卡格列净的抗增殖作用。卡格列净抑制的受 HDAC2 调节的基因与多个临床 NSCLC 数据集的不良预后相关。此外,我们还提供了证据表明卡格列净还可以改善 NSCLC 对化疗的反应。总之,卡格列净可能是 NSCLC 联合细胞毒性治疗的有前途的治疗方法。