Department of Oncology, Segal Cancer Centre, Lady Davis Institute for Medical Research, Center for Experimental Therapeutics in Cancer, Sir Mortimer B. Davis-Jewish General Hospital, McGill University, 3755 Cote Sainte Catherine Road, Montréal, QC, H3T 1E2, Canada.
Cancer Chemother Pharmacol. 2010 Aug;66(3):467-74. doi: 10.1007/s00280-009-1182-7. Epub 2009 Nov 26.
Nrf2 is a key transcription factor, which induces a cytoprotective gene array. Nrf2 is regulated at the posttranslational level through proteasomal degradation through an interaction with the adapter protein Keap1. High levels of Nrf2, resulting from a loss of function mutation in Keap1, were reported in chemoresistant non-small cell lung cancer. We observed very low levels of Nrf2 and of Nrf2-regulated detoxification proteins as a frequent phenotype in the more chemosensitive breast cancer, and when engineering increased Nrf2 levels, we found resistance to both doxorubicin and paclitaxel. We here show that basal Nrf2 levels in different cell lines correlate with their respective sensitivity to a common cytotoxic chemotherapy. Nrf2 and its regulated genes and proteins are the targets of a major strategy in cancer prevention. Molecules that interfere with the Nrf2-Keap1-Cul3 protein-protein interactions result in higher levels of Nrf2. Both naturally occurring and synthetic molecules with this effect have been suggested as clinical chemopreventive agents, including molecules derived from cruciferous vegetables such as the isothiocyanate sulforaphane and even green tea polyphenols. Here, we determine the impact of these putative chemopreventive agents on the sensitivity of established cancer cell lines to chemotherapy. We confirmed that these molecules do increase Nrf2 and detoxification enzyme levels in breast cancer cell lines with very low basal Nrf2 levels, and this is associated with significant chemoresistance to cytotoxic drugs. Both effects are less in another breast cancer cell line with intermediate Nrf2, and in lung cancer cells with high Nrf2, these same molecules have no effect on Nrf2 but do actually enhance chemoresistance. While the details of dose and schedule of these agents require further study in in vivo models, these data sound a cautionary note for the use of these agents in patients with established cancers who are undergoing chemotherapy treatment.
Nrf2 是一种关键的转录因子,可诱导细胞保护性基因阵列。Nrf2 通过与适配器蛋白 Keap1 的相互作用,在翻译后水平通过蛋白酶体降解进行调节。在化学抗性非小细胞肺癌中,报道了 Keap1 功能丧失突变导致的 Nrf2 水平升高。我们观察到在更具化学敏感性的乳腺癌中,Nrf2 和 Nrf2 调节的解毒蛋白水平非常低,这是一种常见表型,并且当我们设计增加 Nrf2 水平时,我们发现对阿霉素和紫杉醇都有耐药性。我们在这里表明,不同细胞系中的基础 Nrf2 水平与其对常见细胞毒性化疗的敏感性相关。Nrf2 及其调节的基因和蛋白是癌症预防的主要策略的靶点。干扰 Nrf2-Keap1-Cul3 蛋白-蛋白相互作用的分子会导致 Nrf2 水平升高。具有这种作用的天然和合成分子已被提议作为临床化学预防剂,包括源自十字花科蔬菜的分子,如异硫氰酸酯萝卜硫素,甚至绿茶多酚。在这里,我们确定这些假定的化学预防剂对已建立的癌细胞系对化疗敏感性的影响。我们证实,这些分子确实会增加基础 Nrf2 水平非常低的乳腺癌细胞系中的 Nrf2 和解毒酶水平,这与细胞毒性药物的显着化学抗性相关。在 Nrf2 水平中等的另一种乳腺癌细胞系中和 Nrf2 水平高的肺癌细胞系中,这些相同的分子对 Nrf2 没有影响,但实际上增强了化学抗性。虽然这些药物的剂量和方案细节需要在体内模型中进一步研究,但这些数据为正在接受化疗的已建立癌症患者使用这些药物发出了警告。