LGALS3BP is a novel and potential biomarker in clear cell renal cell carcinoma

被引:0
作者
Li, Lei [1 ]
Qin, Sen [2 ]
Tan, Hongwei [3 ]
Zhou, Jiexue [3 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Urol, Wuhan, Hubei, Peoples R China
[2] First Peoples Hosp Jingzhou, Dept Intervent Radiol, Jingzhou, Hubei, Peoples R China
[3] Guangdong Second Prov Gen Hosp, Dept Organ Transplantat, Guangzhou, Guangdong, Peoples R China
来源
AGING-US | 2024年 / 16卷 / 04期
关键词
bioinformatics; biomarkers; LGALS3BP; clear cell renal cell carcinoma; drug screening; BREAST-CANCER CELLS; 3; BINDING-PROTEIN; THERAPEUTIC TARGET; PROGNOSTIC VALUE; POOR SURVIVAL; 90K; EXPRESSION; ANTIGEN; IDENTIFICATION; ANGIOGENESIS;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Clear cell renal cell carcinoma (ccRCC) is the most common solid renal tumor. Therefore, it is necessary to explore the related tumor markers. LGALS3BP (galectin 3 binding protein) is a multifunctional glycoprotein implicated in immunity and cancer. Some studies have shown that LGALS3BP promotes the occurrence and development of tumors. However, their exact role in renal tumorigenesis remains unclear. Our study used a webserver to explore the mRNA expression and clinical features of LGALS3BP in ccRCC. Survival analysis showed that patients with high LGALS3BP expression had significantly worse OS and DFS than those with low LGALS3BP expression. LGALS3BP expression is significantly related to B cells, CD4+ T cells, macrophages, neutrophils, and dendritic cells. Furthermore, we determined that LGALS3BP is significantly associated with angiogenesis, stemness and proliferation in renal cancer. Three phenotypes may be associated with a poor prognosis. Genes related to proliferation, angiogenesis and stemness were derived from a Venn diagram of FGF2. FGF2 is negatively correlated with proliferation and positively correlated with angiogenesis. Finally, we screened for drugs that may have potential therapeutic value for ccRCC. The PCR results showed that the expression of LGALS3BP in the normal cell line was lower than that in the tumor cell lines. After LGALS3BP knockdown, the proliferation of 769-P and 786-O cells decreased. The present findings show that LGALS3BP is critical for ccRCC cell proliferation and may be a potential target and biomarker for ccRCC.
引用
收藏
页码:4033 / 4051
页数:19
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