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RBL1启动子的甲基化增强了三维培养癌细胞的放射抗性。

Methylation of promoter of RBL1 enhances the radioresistance of three dimensional cultured carcinoma cells.

作者信息

Pan Dong, Chen Yaxiong, Du Yarong, Ren Zhenxin, Li Xiaoman, Hu Burong

机构信息

Key Laboratory of Heavy Ion Radiation Biology and Medicine of Chinese Academy of Sciences & Key Laboratory of Space Radiobiology of Gansu Province, Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou, China.

University of Chinese Academy of Sciences, Beijing, China.

出版信息

Oncotarget. 2017 Jan 17;8(3):4422-4435. doi: 10.18632/oncotarget.12647.

Abstract

Three dimensional (3D) culture in vitro is a new cell culture model that more closely mimics the physiology features of the in vivo environment and is being used widely in the field of medical and biological research. It has been demonstrated that cancer cells cultured in 3D matrices are more radioresistant compared with cells in monolayer (2D). However, the mechanisms causing this difference remain largely unclear. Here we found that the cell cycle distribution and expression of cell cycle regulation genes in 3D A549 cells are different from the 2D. The higher levels of the promotor methylation of cell cycle regulation genes such as RBL1 were observed in 3D A549 cells compared with cells in 2D. The treatments of irradiation or 5-Aza-CdR activated the demethylation of RBL1 promotor and resulted in the increased expression of RBL1 only in 3D A549 cells. Inhibition of RBL1 enhanced the radioresistance and decreased the G2/M phase arrest induced by irradiation in 2D A549 and MCF7 cells. Overexpression of RBL1 sensitized 3D cultured A549 and MCF7 cells to irradiation. Taken together, to our knowledge, it is the first time to revealthat the low expression of RBL1 due to itself promotor methylation in 3D cells enhances the radioresistance. Our finding sheds a new light on understanding the features of the 3D cultured cell model and its application in basic research into cancer radiotherapy and medcine development.

摘要

三维(3D)体外培养是一种新的细胞培养模型,它更紧密地模拟体内环境的生理特征,正在医学和生物学研究领域中广泛应用。已经证明,与单层(2D)培养的细胞相比,在3D基质中培养的癌细胞具有更高的放射抗性。然而,导致这种差异的机制在很大程度上仍不清楚。在这里,我们发现3D培养的A549细胞的细胞周期分布和细胞周期调控基因的表达与2D培养的细胞不同。与2D培养的细胞相比,在3D培养的A549细胞中观察到细胞周期调控基因如RBL1的启动子甲基化水平更高。辐射或5-氮杂-2'-脱氧胞苷处理激活了RBL1启动子的去甲基化,并仅在3D培养的A549细胞中导致RBL1表达增加。抑制RBL1增强了2D培养的A549和MCF7细胞的放射抗性,并降低了辐射诱导的G2/M期阻滞。过表达RBL1使3D培养的A549和MCF7细胞对辐射敏感。综上所述,据我们所知,这是首次揭示3D培养细胞中由于其自身启动子甲基化导致的RBL1低表达增强了放射抗性。我们的发现为理解3D培养细胞模型的特征及其在癌症放射治疗基础研究和医学发展中的应用提供了新的线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36bb/5354843/8cd32768a270/oncotarget-08-4422-g001.jpg

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