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作 者:陈中 张嘉玲[2] 杨歆萍 吕海[3] CARTER Van Waes
机构地区:[1]美国马里兰州百萨思达市、国立医学科学研究院、耳鼻喉及交流障碍研究所、头颈外科 [2]内蒙古医科大学附属医院临床医学研究中心 [3]南方医科大学珠江医院骨科中心
出 处:《内蒙古医科大学学报》2013年第1期57-62,共6页Journal of Inner Mongolia Medical University
摘 要:抑癌基因TP53在调控细胞周期、细胞凋亡和维持基因组稳定的过程中发挥着重要作用。TP63和TP73是TP53家族中包含的另外两个成员,均具有多种亚型,这些亚型通过自身家族或与其它转录因子家族之间的相互作用,从而对广泛的基因群发挥调控作用。本文将综述TP53及其家族成员TP63、TP73的功能学研究上的最新进展,并将重点介绍我们NIH/NIDCD头颈外科实验室的近期的研究工作所取得的新发现。我们近期的研究结果揭示了在肿瘤炎症的微环境中,存在着一种新的可逆转的动态机制为促炎症细胞因子TNF-α诱导NF-κB c-REL/ΔNp 63α相互作用,协同促进细胞增殖、生存、炎症和迁移相关基因群的调控。并在有突变的TP53肿瘤中,这些相互作用同时使肿瘤抑制基因TAp73的功能失活,促进肿瘤对TNF-α的抗药性和细胞生存。我们的研究阐述了炎症与肿瘤发生、发展的新机制,其中NF-κB和TP53两大转录因子家族基因的相互作用起到了关键性作用。这一新发现或许可为肿瘤的诊断、治疗和预防提供新的策略。As a tumor suppressor, TP53 plays genome stability. DNA-damaging agents activate the a crucial role in the cell cycle, apoptosis, and TP53 signaling pathway and lead cells either in cell cycle arrest to allow DNA repair,or induce cell apoptosis. The rate of TP53 mutation is extremely high in cancer, so that it not only abrogates TP53 tumor-suppressive functions, but may also alter or gain functions to promote oncogenesis. TP53 has other family members, including TP63 and TP73, and their isoforms are capable of regulating a broad gene programs, primarily through interactions within their family members, or with other transcription factors families. In this review, we summarize the current knowledge of TP53, TP63 and TP73 family members, and highlight recent novel findings from our laboratory (Head and Neck Surgery Branch, National Institute on Deafness and CommunicationDisorders, National Institutes of Health ). Our findings unveil a novel and reversible dynamic mechanism in the inflammatory tumor microenvironment, whereby proinflammatory cytokine TNF-α induces NF-κB c-REL/△Np 63α interactions to promote a broad gene program involved in cell prolif- eration, survival, inflammation and migration. This interaction also inhibits tumor suppressor TAp 73 function,promoting TNF-α resistance and cell survival in cancers with mutant TP53. Our findings provide a novel connection between inflammation and cancer survival through two families of transcription factors, TP53 and NF-κB, which may lead to a new strategy for cancer prevention, diagnostics and therapy.
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