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白细胞介素-6/信号转导与转录激活因子3/ Twist抑制可逆转电离辐射诱导的食管鳞状细胞癌上皮-间质转化和放射抗性。

IL-6/STAT3/TWIST inhibition reverses ionizing radiation-induced EMT and radioresistance in esophageal squamous carcinoma.

作者信息

Zang Chunbao, Liu Xujie, Li Bing, He Yanqiong, Jing Shen, He Yujia, Wu Wenli, Zhang Bingqian, Ma Shuhong, Dai Weiwei, Li Shaolin, Peng Zhiping

机构信息

Department of Radiological Medicine, Chongqing Medical University, Chonging, China.

Department of Otorhinolaryngology, The First Affiliated Hospital of Chonqqing Medical University, Chongqing, China.

出版信息

Oncotarget. 2017 Feb 14;8(7):11228-11238. doi: 10.18632/oncotarget.14495.

Abstract

The acquisition of radioresistance by esophageal squamous carcinoma (ESC) cells during radiotherapy may lead to cancer recurrence and poor survival. Previous studies have demonstrated that ionizing radiation (IR) induces epithelial-mesenchymal transition (EMT) of ESC cells accompanied by increased migration, invasion, and radioresistance. However, the underlying molecular mechanisms of IR-induced EMT and radioresistance are not well established, hampering the development of potential solutions. To address this issue, we investigated the role of the IL-6/STAT3/TWIST signaling pathway in IR-induced EMT. We found not only the pathway was activated during IR-induced EMT but also STAT3 inhibition or Twist depletion reversed the EMT process and attenuated radioresistance. These results improve our understanding of the underlying mechanisms involved in IR-induced EMT and suggest potential interventions to prevent EMT-induced acquisition of radioresistance.

摘要

食管鳞状癌细胞(ESC)在放疗期间获得放射抗性可能导致癌症复发和生存率低下。先前的研究表明,电离辐射(IR)可诱导ESC细胞发生上皮-间质转化(EMT),同时迁移、侵袭能力增强以及放射抗性增加。然而,IR诱导EMT和放射抗性的潜在分子机制尚未完全明确,这阻碍了潜在解决方案的开发。为了解决这一问题,我们研究了IL-6/STAT3/TWIST信号通路在IR诱导EMT中的作用。我们发现,不仅该通路在IR诱导的EMT过程中被激活,而且抑制STAT3或敲低Twist可逆转EMT过程并减弱放射抗性。这些结果增进了我们对IR诱导EMT潜在机制的理解,并提示了预防EMT诱导的放射抗性获得的潜在干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7054/5355260/ced3b019d386/oncotarget-08-11228-g001.jpg

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