Association between the methylation of CpG islands in JAK-STAT pathway-related genes and colorectal cancer

被引:2
作者
Rong, Jiesheng [1 ]
Pu, Rui [2 ]
Sun, Hongru [2 ]
Liu, Yupeng [2 ]
Tian, Tian [2 ]
Bi, Haoran [2 ]
Xia, Tingting [2 ]
Zhang, Lei [2 ]
Zhang, Yuanyuan [2 ]
Zhao, Yashuang [2 ,3 ]
Zhu, Lin [2 ,3 ]
机构
[1] Harbin Med Univ, Dept Surg 2, Affiliated Hosp 2, Harbin, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Publ Hlth Coll, Dept Epidemiol, Harbin, Heilongjiang, Peoples R China
[3] Harbin Med Univ, Publ Hlth Coll, Dept Epidemiol, 157 Baojian St,Nangang Dist,Hei Longjiang Prov, Harbin, Peoples R China
基金
中国博士后科学基金;
关键词
Methylation; JAK-STAT; Peripheral blood; Colorectal cancer; Interactive effect; WHOLE-GRAIN CONSUMPTION; EPITHELIAL-MESENCHYMAL TRANSITION; SIGNALING INDUCES APOPTOSIS; CELL-CYCLE ARREST; CONSTITUTIVE ACTIVATION; PROMOTER METHYLATION; ABERRANT METHYLATION; BREAST-CANCER; COLON-CANCER; INHIBITION;
D O I
10.1016/j.gene.2023.147357
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Aberrant promoter methylation of CpG islands plays an important role in carcinogenesis. However, the association between the DNA methylation of JAK-STAT pathway-related genes in peripheral blood leukocytes and colorectal cancer (CRC) susceptibility remains unclear. Methods: We conducted a case-control study of 403 patients with CRC and 419 cancer free controls, and the DNA methylation levels of JAK2, STAT1, STAT3, and SOCS3 in peripheral blood samples from all subjects were assessed using a methylation-sensitive high-resolution melting (MS-HRM) analysis. Results: Compared with controls, the methylation of the JAK2, STAT1 and SOCS3 genes increased the CRC risk (ORadjusted=1.96, 95% CI, 1.12-3.41, P=0.01; ORadjusted=5.37, 95% CI, 3.74-7.71, P<0.01; ORadjusted=3.30, 95% CI, 1.58-6.87, P<0.01). In the multiple CpG site methylation (MCSM) analysis, a high MCSM value denoted an increased CRC risk (ORadjusted=4.97, 95% CI, 3.34-7.37, P<0.01). Conclusion: In peripheral blood, the methylation of JAK2, STAT1, and high levels of MCSM are promising bio-markers for CRC risk.
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页数:7
相关论文
共 51 条
[1]   The relationship between hypomethylation and CpG island methylation in colorectal neoplasia [J].
Bariol, C ;
Suter, C ;
Cheong, K ;
Ku, SL ;
Meagher, A ;
Hawkins, N ;
Ward, R .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 162 (04) :1361-1371
[2]   Inhibition of Caco-2 colon, MCF-7 and Hs578T breast, and DU 145 prostatic cancer cell proliferation by water-soluble black bean condensed tannins [J].
Bawadi, HA ;
Bansode, RR ;
Trappey, A ;
Truax, RE ;
Losso, JN .
CANCER LETTERS, 2005, 218 (02) :153-162
[3]   Single CpG hypermethylation, allele methylation errors, and decreased expression of multiple tumor suppressor genes in normal body cells of mutation-negative early-onset and high-risk breast cancer patients [J].
Boeck, Julia ;
Appenzeller, Silke ;
Haertle, Larissa ;
Schneider, Tamara ;
Gehrig, Andrea ;
Schroeder, Joerg ;
Rost, Simone ;
Wolf, Beat ;
Bartram, Claus R. ;
Sutter, Christian ;
Haaf, Thomas .
INTERNATIONAL JOURNAL OF CANCER, 2018, 143 (06) :1416-1425
[4]   Methylation and microRNA-mediated epigenetic regulation of SOCS3 [J].
Boosani, Chandra S. ;
Agrawal, Devendra K. .
MOLECULAR BIOLOGY REPORTS, 2015, 42 (04) :853-872
[5]   Peripheral blood DNA methylation detected in the BRCA1 or BRCA2 promoter for sporadic ovarian cancer patients and controls [J].
Bosviel, Remy ;
Michard, Emilie ;
Lavediaux, Guillaume ;
Kwiatkowski, Fabrice ;
Bignon, Yves-Jean ;
Bernard-Gallon, Dominique J. .
CLINICA CHIMICA ACTA, 2011, 412 (15-16) :1472-1475
[6]  
BRAY F, 2018, CA-CANCER J CLIN, V68, P394, DOI [DOI 10.3322/CANJCLIN.49.1.33, DOI 10.3322/CAAC.21492]
[7]   Ubiquitous activation of Ras and Jak/Stat pathways in human HCC [J].
Calvisi, DF ;
Ladu, S ;
Gorden, A ;
Farina, M ;
Conner, EA ;
Lee, JS ;
Factor, VM ;
Thorgeirsson, SS .
GASTROENTEROLOGY, 2006, 130 (04) :1117-1128
[8]  
Chatenoud L, 1998, INT J CANCER, V77, P24, DOI 10.1002/(SICI)1097-0215(19980703)77:1<24::AID-IJC5>3.0.CO
[9]  
2-1
[10]   Epigenetic dysregulation of the Jak/STAT pathway by frequent aberrant methylation of SHP1 but not SOCS1 in acute leukaemias [J].
Chim, CS ;
Wong, ASY ;
Kwong, YL .
ANNALS OF HEMATOLOGY, 2004, 83 (08) :527-532