Prognostic value of integrin variants and expression in postoperative patients with HBV-related hepatocellular carcinoma

被引:12
|
作者
Shang, Liming [1 ]
Ye, Xinping [1 ]
Zhu, Guangzhi [1 ]
Su, Hao [1 ]
Su, Zhixiong [1 ]
Chen, Bin [1 ]
Xiao, Kaiyin [1 ]
Li, Lequn [2 ]
Peng, Minhao [1 ]
Peng, Tao [1 ]
机构
[1] Guangxi Med Univ, Dept Hepatobiliary Surg, Affiliated Hosp 1, Nanning, Peoples R China
[2] Guangxi Med Univ, Dept Hepatobiliary Surg, Affiliated Tumor Hosp, Nanning, Peoples R China
基金
中国国家自然科学基金;
关键词
integrin; SNPs; ITGA5; ITGB5; hepatocellular carcinoma; PROLIFERATION; ANGIOGENESIS; DIAGNOSIS; ACTIVATION; THROMBUS; OUTCOMES; TARGETS; GROWTH; ROLES; CHINA;
D O I
10.18632/oncotarget.20161
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Integrins are a large family of cell surface receptors that bind extracellular matrix proteins and participate in cancer progression. However, the prognostic value of integrin family genes in post-operative patients with HBV-related hepatocellular carcinoma (HCC) remains unknown. In this study, we investigated 18 single nucleotide polymorphisms (SNPs) in integrin family genes and found that the AG/GG genotypes at rs988574 in ITGA1 predicted a better prognosis compared to carriers of the AA genotype (P = 0.025, HR = 0.69, 95% CI = 0.50-0.96). Moreover, rs988574 genotype combined with serum level of AFP had a better prognostic value in HBV-related HCC patients (P = 0.026, HR = 1.75, 95% CI = 1.07-2.85). Furthermore, we compared the expression of 24 integrin family genes in HBV-related HCC tissues and adjacent normal tissues. Survival analysis demonstrated that expression of three of the family members, ITGA5, ITGB5 and ITGA2B, were significantly associated with the overall survival (OS) or relapse-free survival (RFS) of HBV-related HCC patients. Additionally, patients with lower expression of both ITGA5 and ITGB5 had the best OS and RFS (P = 0.017 and P = 0.002, respectively). Our study demonstrated that rs988574 of ITGA1 and the expression of ITGA5, ITGB5 and ITGA2B are potential independent prognostic bio-markers and therapeutic targets for HBV-related HCC patients and may be useful for the diagnosis of HBV-related HCC.
引用
收藏
页码:76816 / 76831
页数:16
相关论文
共 50 条
  • [41] Genetic variants in m5C modification genes are associated with survival of patients with HBV-related hepatocellular carcinoma
    Chen, Bowen
    Qiu, Moqin
    Gong, Rongbin
    Liu, Yingchun
    Zhou, Zihan
    Wen, Qiuping
    Wei, Xiaoxia
    Liang, Xiumei
    Jiang, Yanji
    Chen, Peiqin
    Wei, Yuying
    Huang, Qiongguang
    Mo, Qiuyan
    Lin, Qiuling
    Yu, Hongping
    ARCHIVES OF TOXICOLOGY, 2024, 98 (4) : 1125 - 1134
  • [42] Genetic variants in m5C modification genes are associated with survival of patients with HBV-related hepatocellular carcinoma
    Bowen Chen
    Moqin Qiu
    Rongbin Gong
    Yingchun Liu
    Zihan Zhou
    Qiuping Wen
    Xiaoxia Wei
    Xiumei Liang
    Yanji Jiang
    Peiqin Chen
    Yuying Wei
    Qiongguang Huang
    Qiuyan Mo
    Qiuling Lin
    Hongping Yu
    Archives of Toxicology, 2024, 98 : 1125 - 1134
  • [43] Peritumoral EpCAM Is an Independent Prognostic Marker after Curative Resection of HBV-Related Hepatocellular Carcinoma
    Dai, Xiao-Meng
    Huang, Tao
    Yang, Sheng-Li
    Zheng, Xiu-Mei
    Chen, George G.
    Zhang, Tao
    DISEASE MARKERS, 2017, 2017
  • [44] Prognostic Value of TP53 Mutation for Transcatheter Arterial Chemoembolization Failure/Refractoriness in HBV-Related Advanced Hepatocellular Carcinoma
    Xue, Miao
    Wu, Yanqin
    Fan, Wenzhe
    Guo, Jian
    Wei, Jialiang
    Wang, Hongyu
    Tan, Jizhou
    Wang, Yu
    Yao, Wang
    Zhao, Yue
    Li, Jiaping
    CANCER RESEARCH AND TREATMENT, 2020, 52 (03): : 925 - 937
  • [45] Obstacles and opportunities in the prevention and treatment of HBV-related hepatocellular carcinoma
    Liao, Yong
    GENES & DISEASES, 2020, 7 (03) : 291 - 298
  • [46] Does chemotherapy prevent HBV-related hepatocellular carcinoma? Pros
    Liaw, Yun-Fan
    DIGESTIVE AND LIVER DISEASE, 2010, 42 : S293 - S297
  • [47] Does chemotherapy prevent HBV-related hepatocellular carcinoma? Cons
    Colombo, Massimo
    DIGESTIVE AND LIVER DISEASE, 2010, 42 : S298 - S301
  • [48] MUTATION SPECTRUM ASSOCIATED WITH THE PROGRESSION OF HBV-RELATED HEPATOCELLULAR CARCINOMA
    Woo, H. G.
    Kim, S. S.
    Cho, H. W.
    Kwon, S. M.
    Cho, H. J.
    Ahn, S. J.
    Cho, S. W.
    Cheong, J. Y.
    JOURNAL OF HEPATOLOGY, 2014, 60 (01) : S88 - S88
  • [49] Polymorphisms of FGFR1 in HBV-related hepatocellular carcinoma
    Xie, Haiyang
    Xing, Chunyang
    Wei, Bajin
    Xu, Xiao
    Wu, Liming
    Wu, Jian
    Chen, Leiming
    Cao, Guoqiang
    Chen, Hai
    Meng, Xueqin
    Yin, Shengyong
    Zhou, Lin
    Zheng, Shusen
    TUMOR BIOLOGY, 2015, 36 (11) : 8881 - 8886
  • [50] Host and Viral Genetic Variation in HBV-Related Hepatocellular Carcinoma
    An, Ping
    Xu, Jinghang
    Yu, Yanyan
    Winkler, Cheryl A.
    FRONTIERS IN GENETICS, 2018, 9