Bharti Alok C, Aggarwal Bharat B
Cytokine Research Section, Department of Bioimmunotherapy, M. D. Anderson Cancer Center, University of Texas, Box 143, 1515 Holcomb Boulevard, Houston, TX 77030, USA.
Biochem Pharmacol. 2002 Sep;64(5-6):883-8. doi: 10.1016/s0006-2952(02)01154-1.
Cancer is a hyperproliferative disorder in which invasion and angiogenesis lead to tumor metastasis. Several genes that mediate tumorigenesis and metastasis are regulated by a nuclear transcription factor, nuclear factor kappa B (NF-kappaB). A heterotrimeric complex consisting of p50, p65, and IkappaBalpha, NF-kappaB is present in its inactive state in the cytoplasm. When NF-kappaB is activated, IkappaBalpha is degraded and p50-p65 heterodimer is translocated to the nucleus, binds the DNA (at the promoter region), and activates gene. Research within the last few years has revealed that NF-kappaB is activated by carcinogens, tumor promoters, inflammatory cytokines, and by chemotherapeutic agents. The activation of NF-kappaB can suppress apoptosis, thus promoting chemoresistance and tumorigenesis. Interestingly, however, most chemopreventive agents appear to suppress the activation of the NF-kappaB through inhibition of NF-kappaB signaling pathway. These chemopreventive agents also sensitize the tumors to chemotherapeutic agents through abrogation of NF-kappaB activation. Overall, these observations suggest that NF-kappaB is an ideal target for chemoprevention and chemosensitization. This article reviews evidence supporting this hypothesis.
癌症是一种过度增殖性疾病,其中侵袭和血管生成会导致肿瘤转移。几种介导肿瘤发生和转移的基因受核转录因子核因子κB(NF-κB)调控。NF-κB是一种由p50、p65和IκBα组成的异源三聚体复合物,在细胞质中以无活性状态存在。当NF-κB被激活时,IκBα会降解,p50-p65异二聚体转位至细胞核,与DNA(在启动子区域)结合并激活基因。过去几年的研究表明,NF-κB可被致癌物、肿瘤启动子、炎性细胞因子以及化疗药物激活。NF-κB的激活可抑制细胞凋亡,从而促进化疗耐药性和肿瘤发生。然而,有趣的是,大多数化学预防剂似乎通过抑制NF-κB信号通路来抑制NF-κB的激活。这些化学预防剂还通过消除NF-κB激活使肿瘤对化疗药物敏感。总体而言,这些观察结果表明NF-κB是化学预防和化学增敏的理想靶点。本文综述了支持这一假说的证据。