The Contribution of Matrix Metalloproteinase-7 Promoter Genotypes to Hepatocellular Carcinoma Susceptibility

被引:3
|
作者
Yueh, Te-cheng [1 ,2 ,3 ]
Tsao, Hao-yuan [4 ]
Chien, Wei-ching [5 ]
Tsai, Chia-wen [1 ,6 ]
Pei, Jen-sheng [7 ]
Wu, Ming-hsien [1 ,2 ,3 ]
Chen, Chou-pin [8 ]
Chen, Chou-chen [8 ]
Wang, Zhi-hong [9 ]
Mong, Mei-chin [9 ]
Yang, Ya-chen [9 ]
Hung, Yi-chih [6 ]
Bau, Da -tian [1 ,6 ,10 ,11 ]
Chang, Wen-shin [1 ,6 ,11 ]
机构
[1] China Med Univ, Grad Inst Biomed Sci, Taichung, Taiwan
[2] Taichung Armed Forces Gen Hosp, Div Colon & Rectal Surg, Taichung, Taiwan
[3] Natl Def Med Ctr, Taipei, Taiwan
[4] Chang Bing Show Chwan Mem Hosp, Dept Family Med, Changhua, Taiwan
[5] Chang Bing Show Chwan Mem Hosp, Cell Therapy Ctr, Changhua, Taiwan
[6] China Med Univ Hosp, Dept Med Res, Terry Fox Canc Res Lab, Taichung, Taiwan
[7] Taoyuan Gen Hosp, Minist Hlth & Welf, Dept Pediat, Taoyuan, Taiwan
[8] Taichung Vet Gen Hosp, Dept Surg, Taichung, Taiwan
[9] Asia Univ, Dept Food Nutr & Hlth Biotechnol, Taichung, Taiwan
[10] Asia Univ, Dept Bioinformat & Med Engn, Taichung, Taiwan
[11] China Med Univ Hosp, Terry Fox Canc Res Lab, 2 Yuh Der Rd, Taichung 404, Taiwan
关键词
Genotype; hepatocellular carcinoma; MMP-7; polymorphism; HCC; Taiwan; SQUAMOUS-CELL CARCINOMA; HEPATITIS-B-VIRUS; COLORECTAL-CANCER; TISSUE INHIBITOR; CIGARETTE-SMOKING; GASTRIC-CANCER; DIFFERENTIAL EXPRESSION; FUNCTIONAL POLYMORPHISM; GENETIC POLYMORPHISMS; TUMOR PROGRESSION;
D O I
10.21873/anticanres.16034
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Metalloproteinase-7 (MMP-7) has been previously found to be up-regulated in hepatocellular carcinoma (HCC) specimens and cells, favoring epithelial- mesenchymal transition. However, the contribution of MMP-7 genotypes to HCC has not been revealed to date. The study aimed to evaluate the contribution of MMP-7 promoter A-181G (rs11568818) and C-153T (rs11568819) genotypes on the risk of HCC in Taiwan, where HCC incidence is extremely high compared to worldwide data. Materials and Methods: In this case-control study, MMP-7 genotypes and their association with cigarette smoking and alcohol drinking habits were determined in 298 HCC patients and 889 healthy subjects by a typical polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) methodology. Results: Ever smokers and alcohol drinkers were represented with higher percentages in the case group compared to the control group. MMP-7 rs11568818 genotypes were not found differentially distributed in case and control groups (p for trend=0.5246). People of the analyzed cohort of the present study were all of CC genotypes at their rs11568819 polymorphic sites, without any CT or TT genotypes. As for gene-lifestyle interactions, people with variant genotypes at MMP-7 rs11568818 had the same odds for HCC development compared to the wild-type AA genotype, no matter whether the subjects belonged to the smoker, non-smoker alcohol drinker, or non-drinker groups. Conclusion: MMP-7 variant genotypes did not present any significance towards being a marker for HCC risk in Taiwanese.
引用
收藏
页码:5275 / 5282
页数:8
相关论文
共 50 条
  • [21] Elevated matrix metalloproteinase-7 expression promotes metastasis in human lung carcinoma
    Han, Ji-Chang
    Li, Xian-Dong
    Du, Jin
    Xu, Feng
    Wei, Yu-Ju
    Li, Hong-Bing
    Zhang, Yi-Jie
    WORLD JOURNAL OF SURGICAL ONCOLOGY, 2015, 13
  • [22] Polymorphisms of matrix metalloproteinase-7 and chymase are associated with susceptibility to and progression of gastric cancer in Japan
    Mitsushige Sugimoto
    Takahisa Furuta
    Chise Kodaira
    Masafumi Nishino
    Mihoko Yamade
    Mutsuhiro Ikuma
    Haruhiko Sugimura
    Akira Hishida
    Journal of Gastroenterology, 2008, 43 : 751 - 761
  • [23] The Contribution of Matrix Metalloproteinase-1 Genotype to Oral Cancer Susceptibility in Taiwan
    Sun, Kuo-Ting
    Tsai, Chia-Wen
    Chang, Wen-Shin
    Shih, Liang-Chun
    Chen, Liang-Yu
    Tsai, Ming-Hsiu
    Ji, Hong-Xue
    Hsiao, Chieh-Lun
    Liu, Yu-Cheng
    Li, Chi-Yuan
    Bau, Da-Tian
    IN VIVO, 2016, 30 (04): : 439 - 444
  • [24] Matrix Metalloproteinase-7 Promoter Site Single Nucleotide Polymorphism (-181A>G) in Epithelial Ovarian Cancer in the Eastern Indian Population
    Anudeep, P. P.
    Kumari, Suchitra
    Dasmajumdar, Saroj
    Mangaraj, Manaswini
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (03)
  • [25] Impacts of Matrix Metalloproteinase 9 Genotypes on Renal Cell Carcinoma
    Liao, Cheng-hsi
    Tsai, Chung-lin
    Chang, Shu-yu
    Lin, Yu-hsin
    Wang, Yun-chi
    Huang, Wen-chin
    Mong, Mei-chin
    Yang, Ya-chen
    Wu, Wen-tzu
    Chen, Jaw-chyun
    Tsai, Chia-wen
    Bau, Da-tian
    Chang, Wen-shin
    IN VIVO, 2023, 37 (06): : 2452 - 2458
  • [26] The Contribution of Interleukin-10 Promoter Genotypes to Susceptibility to Asthma in Adults
    Hsia, Te-Chun
    Chang, Wen-Shin
    Wang, Shengyu
    Shen, Te-Chun
    Hsiao, Wan-Yun
    Liu, Chin-Jung
    Liang, Shinn-Jye
    Chen, Wei-Chun
    Tu, Chih-Yen
    Tsai, Chia-Wen
    Hsu, Chin-Mu
    Bau, Da-Tian
    IN VIVO, 2015, 29 (06): : 695 - 699
  • [27] Contribution of Matrix Metalloproteinase-9 rs3918242 Genotypes to Childhood Leukemia Risk
    Kuo, Chien-Chung
    Tsai, Chia-Wen
    Chang, Wen-Shin
    Shen, Te-Chun
    Tzeng, Huey-En
    Li, Chia-Hsiang
    Wang, Yun-Chi
    Tsai, Fuu-Jen
    Bau, Da-Tian
    ANTICANCER RESEARCH, 2020, 40 (10) : 5751 - 5756
  • [28] Fibulin-5 inhibits hepatocellular carcinoma cell migration and invasion by down-regulating matrix metalloproteinase-7 expression
    Tu, Kangsheng
    Dou, Changwei
    Zheng, Xin
    Li, Chao
    Yang, Wei
    Yao, Yingmin
    Liu, Qingguang
    BMC CANCER, 2014, 14
  • [29] Fibulin-5 inhibits hepatocellular carcinoma cell migration and invasion by down-regulating matrix metalloproteinase-7 expression
    Kangsheng Tu
    Changwei Dou
    Xin Zheng
    Chao Li
    Wei Yang
    Yingmin Yao
    Qingguang Liu
    BMC Cancer, 14
  • [30] Association of Matrix Metalloproteinase-9 rs3918242 Promoter Genotypes With Colorectal Cancer Risk
    Wu, Ming-Hsien
    Tzeng, Huey-En
    Wu, Cheng-Nan
    Yueh, Te-Cheng
    Peng, Yen-Chun
    Tsai, Chun-Hao
    Wang, Yun-Chi
    Ke, Tao-Wei
    Pei, Jen-Sheng
    Chang, Wen-Shin
    Tsai, Chia-Wen
    Bau, Da-Tian
    ANTICANCER RESEARCH, 2019, 39 (12) : 6523 - 6529