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SMYD3 相关的癌症调控通路。

Smyd3-associated regulatory pathways in cancer.

机构信息

Biomedical Sciences Research Center Alexander Fleming, 16672 Vari, Greece.

Biomedical Sciences Research Center Alexander Fleming, 16672 Vari, Greece.

出版信息

Semin Cancer Biol. 2017 Feb;42:70-80. doi: 10.1016/j.semcancer.2016.08.008. Epub 2016 Aug 21.

Abstract

SMYD3 is a member of the SET and MYND-domain family of methyl-transferases, the increased expression of which correlates with poor prognosis in various types of cancer. In liver and colon tumors, SMYD3 is localized in the nucleus, where it interacts with RNA Pol II and H3K4me3 and functions as a selective transcriptional amplifier of oncogenes and genes that control cell proliferation and metastatic spread. Smyd3 expression has a high discriminative power for the characterization of liver tumors and positively correlates with poor prognosis. In lung and pancreatic cancer, SMYD3 acts in the cytoplasm, potentiating oncogenic Ras/ERK signaling through the methylation of the MAP3K2 kinase and the subsequent release from its inhibitor. A clinico-pathological analysis of lung cancer patients uncovers prognostic significance of SMYD3 only for first progression survival. However, stratification of patients according to their smoking history significantly expands the prognostic value of SMYD3 to overall survival and other features, suggesting that smoking-related effects saturate the clinical analysis and mask the function of SMYD3 as an oncogenic potentiator.

摘要

SMYD3 是 SET 和 MYND 结构域家族的甲基转移酶成员,其表达增加与各种类型癌症的预后不良相关。在肝脏和结肠肿瘤中,SMYD3 定位于细胞核内,与 RNA Pol II 和 H3K4me3 相互作用,作为癌基因和控制细胞增殖和转移扩散的基因的选择性转录放大器发挥作用。Smyd3 表达对肝脏肿瘤的特征具有很高的区分能力,并与预后不良呈正相关。在肺癌和胰腺癌中,SMYD3 在细胞质中发挥作用,通过 MAP3K2 激酶的甲基化及其抑制剂的释放,增强致癌性 Ras/ERK 信号。对肺癌患者的临床病理分析揭示了 SMYD3 仅对首次进展生存具有预后意义。然而,根据患者的吸烟史进行分层显著扩大了 SMYD3 对总生存和其他特征的预后价值,表明与吸烟相关的影响使临床分析饱和,掩盖了 SMYD3 作为致癌增强剂的功能。

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