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NRF2基因的遗传多态性作为癌症化疗的预后标志物。

Genetic polymorphism in the NRF2 gene as a prognosis marker for cancer chemotherapy.

作者信息

Ishikawa Toshihisa

机构信息

Personalized Medicine Research Institute, NGO Personalized Medicine and Healthcare, Yokohama Japan ; RIKEN Center for Life Science Technologies, Yokohama Japan.

出版信息

Front Genet. 2014 Nov 4;5:383. doi: 10.3389/fgene.2014.00383. eCollection 2014.

Abstract

NF-E2-related factor 2 (NRF2) is a transcription factor that controls the expression of a variety of antioxidant and detoxification genes. Accumulating evidence strongly suggests that NRF2 mediates cancer cell proliferation and drug resistance, as well. Single nucleotide polymorphism (SNP) -617C > A in the anti-oxidant response element-like loci of the human NRF2 gene play a pivotal role in the positive feedback loop of transcriptional activation of the NRF2 gene. Since the SNP (-617A) reportedly decreases the binding affinity to the transcription factors of NRF2/small multiple alignment format (MafK), the homozygous -617A/A allele may attenuate the positive feedback loop of transcriptional activation of the NRF2 gene and reduce the NRF2 protein level. As the consequence, cancer cells are considered to become more sensitive to therapy and less aggressive than cancer cells harboring the -617C (WT) allele. Indeed, Japanese lung cancer patients carrying SNP homozygous alleles (c. -617A/A) exhibited remarkable survival over 1,700 days after surgical operation (log-rank p = 0.021). The genetic polymorphism in the human NRF2 gene is considered as one of prognosis markers for cancer therapy.

摘要

核因子E2相关因子2(NRF2)是一种转录因子,可控制多种抗氧化和解毒基因的表达。越来越多的证据有力地表明,NRF2也介导癌细胞的增殖和耐药性。人类NRF2基因抗氧化反应元件样位点的单核苷酸多态性(SNP)-617C>A在NRF2基因转录激活的正反馈回路中起关键作用。据报道,由于SNP(-617A)降低了与NRF2/小多重比对格式(MafK)转录因子的结合亲和力,纯合-617A/A等位基因可能会减弱NRF2基因转录激活的正反馈回路并降低NRF2蛋白水平。因此,与携带-617C(野生型)等位基因的癌细胞相比,癌细胞被认为对治疗更敏感且侵袭性更低。事实上,携带SNP纯合等位基因(c.-617A/A)的日本肺癌患者在手术后1700多天表现出显著的生存率(对数秩检验p=0.021)。人类NRF2基因的遗传多态性被认为是癌症治疗的预后标志物之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2776/4219421/59cd86abd054/fgene-05-00383-g001.jpg

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