Smithsonian Marine Station , 701 Seaway Drive , Fort Pierce , Florida 34949 , United States.
ACS Chem Biol. 2018 May 18;13(5):1189-1199. doi: 10.1021/acschembio.7b01025. Epub 2018 Mar 22.
Resistance to chemotherapy is a major obstacle in the treatment of a wide array of different types of cancer. Chemotherapeutic drug resistance is achieved by cancer cells by a variety of different mechanisms, which can be either compound specific or general. An emerging mechanism for nonspecific chemotherapeutic drug resistance relies on hyperactivity of the transcription factor Nrf2. Normally Nrf2 levels are tightly regulated by the ubiquitin-proteasome system; however, mutations in genes responsible for this regulation are common in many cancer types, resulting in increased expression of Nrf2, activation of its downstream target genes, and resistance to a variety of chemotherapeutic agents. For this reason, there has been considerable interest in the discovery of small molecule inhibitors of Nrf2 capable of attenuating this resistance mechanism. To this end, we have screened two commercially available libraries of known biologically active small molecules to identify potential Nrf2 inhibitors. To increase the breadth of this screen we have also screened an RNAi library that targets the majority of the druggable genome to also identify Nrf2-inhibitor targets that are not currently targeted by small molecules. To complement the commercial chemical and genomic library screening, we screened a small collection of proprietary natural products isolated from marine cyanobacteria, which included actin targeting and uncharacterized but biologically active compounds. Through these efforts, we have identified three classes of compounds: cardiac glycosides, Stat3 inhibitors, and actin disrupting agents as Nrf2 inhibitors that are able to attenuate Nrf2 activity and synergize with chemotherapeutic agents in the non-small-cell lung cancer cell line A549. In addition, we found that grassypeptolide A exerts Nrf2 modulatory activity via a thus far uncharacterized mechanism. Moreover, we have identified a set of putative Nrf2 targets comprising the transcription factors TWIST1 and ELF4, the protein kinase NEK8, the TAK1 kinase regulator TAB1, and the dual specific phosphatase DUSP4. This study broadens the range of mechanisms through which inhibition of Nrf2 activity can be achieved, which will facilitate the characterization of novel Nrf2 inhibitors and allow the design of target specific screening procedures with which to identify more.
化疗耐药性是治疗多种不同类型癌症的主要障碍。癌细胞通过多种不同的机制产生化疗耐药性,这些机制可以是特定化合物的,也可以是一般的。一种新出现的非特异性化疗耐药机制依赖于转录因子 Nrf2 的过度活跃。正常情况下,Nrf2 的水平受泛素-蛋白酶体系统的严格调节;然而,许多癌症类型中负责这种调节的基因发生突变,导致 Nrf2 的表达增加、其下游靶基因的激活以及对多种化疗药物的耐药性。因此,人们对发现能够减弱这种耐药机制的 Nrf2 小分子抑制剂产生了浓厚的兴趣。为此,我们筛选了两种市售的已知生物活性小分子文库,以鉴定潜在的 Nrf2 抑制剂。为了扩大筛选范围,我们还筛选了靶向大部分可用药基因组的 RNAi 文库,以鉴定目前尚未被小分子靶向的 Nrf2 抑制剂靶点。为了补充商业化学和基因组文库筛选,我们筛选了一小部分从海洋蓝藻中分离的专有天然产物,其中包括针对肌动蛋白的化合物和未被表征但具有生物活性的化合物。通过这些努力,我们确定了三类化合物:强心苷、Stat3 抑制剂和肌动蛋白破坏剂,它们都是 Nrf2 抑制剂,能够减弱 Nrf2 活性,并与非小细胞肺癌细胞系 A549 中的化疗药物协同作用。此外,我们发现 grassypeptolide A 通过一种迄今为止尚未被描述的机制发挥 Nrf2 调节活性。此外,我们还鉴定了一组假定的 Nrf2 靶标,包括转录因子 TWIST1 和 ELF4、蛋白激酶 NEK8、TAK1 激酶调节剂 TAB1 和双特异性磷酸酶 DUSP4。这项研究拓宽了抑制 Nrf2 活性的机制范围,这将有助于对新型 Nrf2 抑制剂进行特征描述,并允许设计针对特定靶标的筛选程序,以识别更多的抑制剂。