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Tissue inhibitor matrix metalloproteinase 1 polymorphisms associated with colorectal cancer prognosis in a Han Chinese cohort
被引:0
|作者:
Meng, Chunyan
[1
]
Liu, Jingting
[2
]
Tang, Kaifeng
[1
]
Tang, Hongchao
[1
]
Liao, Jianhua
[1
]
机构:
[1] Zhejiang Hosp, Dept Gen Surg, 12 Lingyin Rd, Hangzhou 310013, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sir Run Run Shaw Hosp, Dept Emergency, Sch Med, 3 Qingchun East Rd, Hangzhou 310020, Zhejiang, Peoples R China
来源:
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE
|
2019年
/
12卷
/
06期
关键词:
Tissue inhibitor matrix metalloproteinase 1;
polymorphism;
prognosis;
colorectal cancer;
biomarker;
TIMP-1;
CELLS;
RISK;
CHEMOTHERAPY;
OVEREXPRESSION;
MARKERS;
PLASMA;
D O I:
暂无
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Purpose: Tissue inhibitor of metalloproteinase-1 (TIMP-1) is an inhibitor of matrix metalloproteinases, known to play a crucial role in tumorigenesis. It has significant predictive value for patients with colorectal cancer (CRC). However, its precise clinical applicability remains unknown. The current study investigated association between TIMP-1 gene polymorphisms and survival in CRC patients. Method: This study enrolled 118 endometrial cancer patients that underwent surgery for CRC between January 2011 and July 2015. Patients were genotyped for TIMP-1 polymorphism (rs4898, 372 T/C). In addition, TIMP-1 levels were assessed using enzyme-linked immunosorbent assay kits. Results: Higher plasma TIMP-1 levels were observed in patients with TIMP-1 rs4898 T allele, compared to patients with non-T alleles (P<0.001). There was significant association with vascular invasion (P=0.002), lymph node metastasis (P=0.038), distant metastasis (P=0.049), TNM stage (P=0.003), Dukes' stage (P=0.045), and recurrence (P=0.005). Kaplan-Meier analysis demonstrated that TIMP-1 rs4898 T allele was associated with lower cumulative overall survival (OS) and recurrence-free survival (RFS) (P<0.001, P<0.001, respectively). Cox proportional hazards modeling showed the TIMP-1 rs4898 T allele to be an independent prognostic predictor for OS (HR=2.607, 95% CI=1.158-5.870, P=0.021) and RFS (HR=2.667, 95% CI=1.194-5.959, P=0.017) in CRC patients. Conclusion: TIMP-1 rs4898 polymorphisms are associated with unfavorable clinicopathological factors, indicating potential clinical predictive value for CRC patient prognosis.
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页码:7717 / 7724
页数:8
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