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Expression and Significance of BCCIP and Glutathione Peroxidase 4 in Clear Cell Renal Cell Carcinoma
被引:0
|作者:
Liu, Yao
[1
]
Liu, J.
[2
]
Liu, C.
[1
]
Jin, J.
[3
]
Liu, Yu
[4
]
机构:
[1] Hebei Med Univ, Dept Pathol, Hosp 4, Shijiazhuang, Hebei, Peoples R China
[2] Langfang Tradit Chinese Med Hosp, Phys Examinat Ctr, Langfang, Hebei, Peoples R China
[3] Hebei Med Univ, Dept Epidemiol Lab, Hosp 4, Shijiazhuang, Hebei, Peoples R China
[4] Hebei Med Univ, Dept Gastrointestinal Surg, Hosp 4, Shijiazhuang, Hebei, Peoples R China
关键词:
clear cell renal cell carcinoma;
BCCIP;
GPX4;
protein;
prognosis;
CANCER;
GENE;
D O I:
10.1007/s10517-024-06025-y
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:
In this retrospective study involving 112 patients with clear cell renal cell carcinoma (ccRCC), we analyzed clinical significance and prognostic value of the expression of BCCIP protein interacting with BRCA2 and CDKN1A and glutathione peroxidase 4 (GPX4). The expressions of mRNA and the corresponding proteins were evaluated using reverse transcription PCR and immunohistochemistry. In comparison with control samples of renal peritumoral tissue, the expressions of BCCIP and its mRNA in the tumor tissues were significantly down-regulated, while the expressions of GPX4 and the corresponding mRNA were significantly up-regulated. The down-regulation of BCCIP expression was closely related to histological grade, TNM stage, and lymph node metastasis (p<0.05). The GPX4 overexpression was closely related to tumor size, TNM stage, and the presence of distant metastasis. The Kaplan-Meier survival analysis showed that tumor size, TNM stage, lymph node metastasis, distant metastasis, expressions of BCCIP and GPX4 correlated with progression-free survival (p<0.05). Multivariate Cox regression showed that down-regulation of BCCIP expression and overexpression of GPX4, TNM stage, and distant metastasis were independent prognostic factors of progression-free survival. Thus, down-regulation of BCCIP expression and overexpression of GPX4 are indicatives of progression of ccRCC with poor prognosis. Hence, the control of expression of these proteins can be considered as a novel target for the treatment of ccRCC.
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页码:394 / 398
页数:5
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