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World J Gastroenterol. Oct 28, 2013; 19(40): 6876-6882
Published online Oct 28, 2013. doi: 10.3748/wjg.v19.i40.6876
Published online Oct 28, 2013. doi: 10.3748/wjg.v19.i40.6876
Overexpression of nuclear β-catenin in rectal adenocarcinoma is associated with radioresistance
Lin Wang, Xiao-Mei Zhang, Zhen Li, Yu-Feng Cheng, Department of Radiation Oncology, Qilu Hospital, Shandong University, Jinan 250012, Shandong Province, China
Xi-Jun Liu, Department of Radiation Oncology, Shandong Tumor Hospital and Institute, Jinan 250117, Shandong Province, China
Jie Chai, Department of General Surgery, Shandong Tumor Hospital and Institute, Jinan 250117, Shandong Province, China
Guang-Yong Zhang, Department of General Surgery, Qilu Hospital, Shandong University, Jinan 250012, Shandong Province, China
Author contributions: Chai J and Zhang GY collected all the human material; Wang L, Zhang XM, Li Z and Liu XJ performed the majority of experiments; Wang L and Cheng YF designed the study and wrote the manuscript.
Supported by Natural Science Foundation of Shandong Province, China, No. ZR2012HQ032; and China Postdoctoral Science Foundation funded project, No. 2013M531614
Correspondence to: Yu-Feng Cheng, MD, Department of Radiation Oncology, Qilu Hospital, Shandong University, 107 Wenhua Xi Road, Jinan 250012, Shandong Province, China. 33943219@qq.com
Telephone: +86-531-82169441 Fax: +86-531-82169441
Received: June 14, 2013
Revised: July 29, 2013
Accepted: September 16, 2013
Published online: October 28, 2013
Processing time: 151 Days and 17.9 Hours
Revised: July 29, 2013
Accepted: September 16, 2013
Published online: October 28, 2013
Processing time: 151 Days and 17.9 Hours
Core Tip
Core tip: In this paper we investigated the relationship between overexpression of nuclear β-catenin in rectal adenocarcinoma and radioresistance. We first confirmed that nuclear β-catenin overexpression in rectal adenocarcinoma is associated with radioresistance. Most importantly, we found that nuclear β-catenin-based prediction achieved a 83% accuracy, 65% sensitivity and 88% specificity for radioresistance. We provided a novel possible molecular mechanism to explain the radioresistance in rectal adenocarcinoma and thus may provide a new therapeutic target for enhancing radiosensitivity.