Association between Higher Expression of Vav1 in Hepatocellular Carcinoma and Unfavourable Clinicopathological Features and Prognosis

被引:0
|
作者
Ye, Weikang [1 ]
Wang, Jin [1 ]
Zheng, Jie [1 ]
Jiang, Ming [1 ]
Zhou, Yinong [1 ]
Wu, Zhixiang [2 ]
机构
[1] Wenzhou Med Univ, Quzhou Peoples Hosp, Dept Gen Surg, Quzhou Affiliated Hosp, Quzhou 324000, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Quzhou Peoples Hosp, Dept Emergency Surg, Quzhou Affiliated Hosp, Quzhou 324000, Zhejiang, Peoples R China
来源
PROTEIN AND PEPTIDE LETTERS | 2024年 / 31卷 / 09期
关键词
Hepatocellular carcinoma; Vav1; protein; Immunohistochemistry; survival analysis; prognosis; SIGNAL TRANSDUCER VAV1; CANCER;
D O I
10.2174/0109298665330781240830042601
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Objective: The aim was to investigate the potential relationship between Vav1 protein and prognosis in patients with hepatocellular carcinoma (HCC). Methods: Samples were collected from 96 patients with HCC. For each patient, cancerous tissue and adjacent non-cancerous tissue were obtained. The Vav1 expression levels in these tissues were determined using immunohistochemistry. Chi-square and Fisher's exact tests were used to analyse the associations between Vav1 expression and clinicopathological characteristics. Kaplan- Meier analysis was used to assess the relationship between Vav1 expression and 5-year overall survival (OS). Results: The expression level of Vav1 protein in primary tumour samples (64.46%; 59/96) was higher (33.33%; 32/96; P<0.001). Moreover, the high expression rate of Vav1 was correlated with tumour differentiation, TNM stage, and tumour recurrence (P<0.05). Univariate and multivariate Cox analysis further demonstrated that tumour differentiation, TNM stage, vascular invasion, tumour recurrence and Vav1 expression were independent prognostic factors for 5-year OS. Notably, follow-up analysis determined that patients with HCC with higher Vav1 expression levels have lower survival rates (P<0.05). Conclusion: Vav1 may serve as a promising molecular prognostic biomarker for patients diagnosed with HCC.
引用
收藏
页码:706 / 713
页数:8
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