z-logo
open-access-imgOpen Access
Significant association of PRMT 6 hypomethylation with colorectal cancer
Author(s) -
Pan Ranran,
Yu Hang,
Dai Jie,
Zhou Cong,
Ying Xiuru,
Zhong Jie,
Zhao Jun,
Zhang Yihan,
Wu Boyi,
Mao Yiyi,
Wu Dongping,
Ying Jieer,
Duan Shiwei
Publication year - 2018
Publication title -
journal of clinical laboratory analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.536
H-Index - 50
eISSN - 1098-2825
pISSN - 0887-8013
DOI - 10.1002/jcla.22590
Subject(s) - methylation , colorectal cancer , biomarker , dna methylation , cancer , methyltransferase , area under the curve , biology , microbiology and biotechnology , medicine , cancer research , biochemistry , gene , gene expression
Background Protein arginine N‐methyltransferase 6 ( PRMT 6) was deemed to be indispensable in the variety of biological processes. Upregulated PRMT 6 was found in various human diseases including cancer. Herein, we investigated the performance of PRMT 6 methylation in the diagnosis for CRC . Methods A quantitative methylation‐specific polymerase chain reaction ( qMSP ) method was used to measure PRMT 6 promoter methylation. The percentage of methylated reference ( PMR ) was applied to represent gene methylation level. Results Our data indicated that PRMT 6 promoter methylation levels were significantly lower in CRC tissues than those in paired nontumor tissues (median PMR : 36.93% vs 63.12%, P  =   1E‐6) and normal intestinal tissues (median PMR : 36.93% vs 506.55%, P  =   8E‐12). We further examined the potential role of PRMT 6 hypomethylation by the receiver operating characteristic ( ROC ) curve. Our results showed that the area under the curve ( AUC ) was 0.644 (95% CI = 0.596‐0.733) between CRC tissues and paired nontumor tissues, 0.958 (95% CI = 0.919‐0.998) between CRC tissues and normal intestinal tissues, and 0.899 (95% CI = 0.825‐0.972) between paired nontumor tissues and normal intestinal tissues. Conclusion Our study firstly indicated that the hypomethylation of PRMT 6 promoter could be a novel diagnostic biomarker for CRC .

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom