Research Papers:
The prognostic significance of protein arginine methyltransferase 6 expression in colon cancer
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Abstract
Yongchul Lim1,*, Suyeun Yu2,*, Jung-A Yun3, In-Gu Do4, Lan Cho5, Yang Hee Kim5 and Hee Cheol Kim1
1Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
2Department of Preventive Medicine, College of Medicine, Korea University, Seoul, Korea
3Department of Surgery, Hanyang University Guri Hospital, Hanyang University College of Medicine, Guri, Korea
4Department of Pathology, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea
5Department of Surgery, Samsung Medical Center, Biomedical Institute, Seoul, Korea
*These authors contributed equally to this work as first authors
Correspondence to:
Hee Cheol Kim, email: [email protected]
Keywords: colon cancer; protein arginine methylation; PRMT6; apoptosis; prognosis
Received: December 07, 2016 Accepted: November 16, 2017 Published: December 27, 2017
ABSTRACT
Protein arginine methylation is involved in cellular differentiation and proliferation. Recently, aberrant expression of protein arginine methyltransferases, which are responsible for the methylation reaction, has been reported in various types of cancer. However, there is no clear evidence regarding the prognostic value of abnormal PRMT6 expression in colorectal cancer or the effect of PRMT6 regulation on CRC cells. We investigated the expression patterns of PRMT6 in patients with stage II and III CRC. We detected nuclear expression of PRMT6 in 23.7% of carcinoma samples by immunohistochemistry. Among the clinicopathological parameters, the ratio of poorly differentiated cancer cells was approximately two-fold higher in patients with PRMT6-positive disease than in those with PRMT6-negative disease (p = 0.002). Patients with PRMT6-positive CRC had a shorter disease-free survival than those with PRMT6-negative CRC in both univariate and multivariate analyses (p = 0.018 and p = 0.035, respectively). siRNA-mediated inhibition of PRMT6 expression in CRC cells induced p21WAF1/CIP1 overexpression and suppressed cell growth and colony-forming ability. Concomitantly, apoptosis was induced in PRMT6-suppressed CRC cells. These data suggest that PRMT6 can serve as a biomarker for unfavorable prognosis and as a therapeutic target in CRC.
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