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β-Catenin、β-Trcp 及CRD-BP与结直肠癌 被引量:1

β-Catenin,β-Trcp and CRD-BP in colorectal cancer
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摘要 Wnt/β-catenin通路在结直肠癌的发生发展过程中起重要作用,其致癌的关键是β-catenin蛋白降解障碍使其在胞内积聚及核易位,并激活下游肿瘤相关性靶基因的转录,不稳定编码区结合蛋白(CRD-BP)是其靶基因之一.在正常细胞中β-catenin降解依赖于β-转导重复相容蛋白(β-Trcp),而在异常细胞中CRD-BP的表达可调控β-Trcp的稳定性.Wnt/β-catenin通路的激活、β-catenin及CRD-BP的高表达、CRD-BP上调β-Trcp与结直肠癌发生、发展及侵袭转移密切相关. Wnt/β-catenin signaling pathway plays an important role in the initiation and progression of colorectal cancer. The key to its carcinogenicity is related to the inhibition of β-catenin degradation, and the subsequent cytoplasmic accumulation and nuclear translocation of β-catenin, which activates the transcription of downstream target genes such as coding region instability determinant-binding protein (CRD-BP). In cancercells ,the expression of CRD-BP mediates the stabilization of β-Trcp, which in normal cells regulates the degradation of β-catenin. The activation of Wnt/β-catenin signaling pathway, overexpression of β-catenin and CRDBP, and the upregulation of β-Trcp by CRD-BP play important roles in the initiation, progression, and metastasis of colorectal cancer.
出处 《国际肿瘤学杂志》 CAS 2010年第8期612-614,共3页 Journal of International Oncology
关键词 结直肠肿瘤 信号传导 Β-CATENIN Colorectal neoplasms Signal transduction β-Catenin
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