期刊文献+

STYK1在恶性肿瘤发生发展中的研究进展

Research progress of STYK1 in occurrence and development of malignant tumors
原文传递
导出
摘要 目的总结丝氨酸苏氨酸酪氨酸激酶1(serine threonine tyrosine kinase 1,STYK1)在肿瘤发生发展中的生物学功能及其分子调控机制。方法检索近年来有关STYK1与肿瘤进展研究的相关文献并进行综述。结果STYK1在多种肿瘤中表达上调并与预后相关,可能通过MEK/ERK、PI3K/AKT、JAK/STAT等信号通路及其靶向蛋白调控肿瘤细胞的增殖、凋亡、迁移、转移、有氧糖酵解、耐药等生物学功能,促进肿瘤的恶性进展。结论STYK1有望成为恶性肿瘤治疗的新靶点,但其调控肿瘤进展的分子机制及其上游调控因子有待进一步挖掘。 Objective To summarize the biological function and molecular regulation mechanism of serine threonine tyrosine kinase 1(STYK1)in tumor occurrence and development.Method The relevant literature about STYK1 and tumor progression in recent years was searched and reviewed.Results The expression of STYK1 was upregulated in a variety of tumors and was related to the prognosis.STYK1 might regulate the proliferation,apoptosis,migration,metastasis,aerobic glycolysis,drug resistance and other biological functions of tumor cells through MEK/ERK,PI3K/AKT,JAK/STAT and their targeting proteins,and promote the malignant progress of tumors.Conclusion STYK1 is expected to become a new target for the treatment of malignant tumors,but the molecular mechanism of its regulation of tumor progression and its upstream regulators need to be further explored.
作者 李俊峰 阮万百 尹艳梅 彭磊 朱克祥 LI Junfeng;RUAN Wanbai;YIN Yanmei;PENG Lei;ZHU Kexiang(The First Clinical Medical College of Lanzhou University,Lanzhou 730000,P.R.China;Department of General Surgery,The First Hospital of Lanzhou University,Lanzhou 730000,P.R.China)
出处 《中国普外基础与临床杂志》 CAS 2023年第10期1258-1264,共7页 Chinese Journal of Bases and Clinics In General Surgery
基金 国家自然科学基金资助项目(项目编号:81960516)。
关键词 丝氨酸苏氨酸酪氨酸激酶1 肿瘤进展 生物学功能 耐药 serine threonine tyrosine kinase 1 tumor progression biological function drug resistance
  • 相关文献

参考文献3

二级参考文献16

  • 1Chen DS, Mellman 1. Oncology meets immunology: the cancer-immunity cycle[ J]. Immunity, 2013,39 : 1 - 10.
  • 2Chen Y, Li YH, Liu L,et al. Point mutation at single tyro- sine residue of novel oncogene NOK abrogates tumorigenesis in nude mice[J]. Cancer Res, 2005,65:10838- 10846.
  • 3Moriai R, Kobayashi D, Amachika T, et al. Diagnostic rel- evance of overexpressed NOK mRNA in breast cancer[ J ]. Anticancer Res, 2006,26:4969 - 4973.
  • 4Li YH, Wang YY, Zhong S, et al. Transmembrane helix of novel oncogene with kinase-domain (NOK) influences its oligomerization and limits the activation of RAS/MAPK sig- naling[J]. Mol CeLls, 2009,27:39 -45.
  • 5Lim S, Kaldis P. Cdks, cyclins and CKIs: roles beyond cell cycle regulation [ J ]. Development, 2013,140 : 3079 - 3093.
  • 6Yu Z, Wang L, Wang C, et al. Cyclin D1 induction of Dic- er governs microRNA processing and expression in breast cancer[ J]. Nat Commun,29:2812 - 2822.
  • 7Xu G, Li Y, Yoshimoto K, et al. 2,3,7,8-Tetrachlorod- ibenzo-p-dioxin stimulates proliferation of HAPI microglia by affecting the Akt/GSK-3β/cyclin D1 signaling pathway [ J]. Toxicol Left, 2013,224:362 - 370.
  • 8Shimura T. Acquired radioresistance of cancer and the AKT/GSK3β/cyclin DI overexpression cycle[ J]. J Radiat Res, 2011,52:539 - 544.
  • 9Bhattacharya S, Das T, Biswas A, et al. A cytotoxic pro- tein (BF-CTI) purified from Bungarus fasciatus venom acts through apoptosis, modulation of PI3K/AKT, MAP- Kinase pathway and cell cycle regulation [ J ]. Toxicon, 2013,74 : 138 - 150.
  • 10李颖华,戎煜,常智杰,刘力.NOK通过JAK2依赖性方式激活STAT3信号通路(英文)[J].生物化学与生物物理进展,2008,35(2):143-150. 被引量:8

共引文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部