Comprehensive analysis of zinc and ring finger 3 in prognostic value and pan-cancer immunity

被引:0
|
作者
Liu, Minghui [1 ,4 ]
Zhao, Huan [1 ]
Peng, Suming [1 ]
Wu, Yunfei [1 ]
Liu, Yanyan [1 ]
Sun, Wu [2 ]
Zen, Ke [3 ,5 ]
Sun, Xinlei [1 ,4 ]
机构
[1] China Pharmaceut Univ, Sch Life Sci & Technol, State Key Lab Nat Med, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Univ, Nanjing Drum Tower Hosp, Affiliated Hosp, Dept Oncol,Med Sch, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Univ, Jiangsu Engn Res Ctr MicroRNA Biol & Biotechnol, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing, Jiangsu, Peoples R China
[4] China Pharmaceut Univ, Sch Life Sci & Technol, State Key Lab Nat Med, 639 Longmian Ave, Nanjing 211198, Jiangsu, Peoples R China
[5] Nanjing Univ, Jiangsu Engn Res Ctr MicroRNA Biol & Biotechnol, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210046, Jiangsu, Peoples R China
关键词
gene alteration; immune infiltration; pan-cancer; prognosis; ZNRF3; GENOMIC CHARACTERIZATION;
D O I
10.1096/fj.202301161R
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
Zinc and ring finger 3 (ZNRF3) is a negative suppressor of Wnt signal and newly identified as an important regulator in tumorigenesis and development. However, the pan-cancer analysis of ZNRF3 has not been reported. We found that ZNRF3 was significantly decreased in six tumors including CESC, KIRP, KIRC, SKCM, OV, and ACC, but increased in twelve tumors, namely LGG, ESCA, STES, COAD, STAD, LUSC, LIHC, THCA, READ, PAAD, TGCT, and LAML. Clinical outcomes of cancer patients were closely related to ZNRF3 expression in ESCA, GBM, KIRC, LUAD, STAD, UCEC, LGG, and SARC. The highest genetic alteration frequency of ZNRF3 occurred in ACC. Abnormal expression of ZNRF3 could be attributed to the differences of copy number variation (CNV) and DNA methylation as well as ZNRF3-interacting proteins. Besides, ZNRF3 were strongly associated with tumor heterogeneity, tumor stemness, immune score, stromal score and ESTIMATE score in certain cancers. In terms of immune cell infiltration, ZNRF3 was positively correlated to infiltration of cancer-associated fibroblasts in CESC, HNSC, OV, PAAD, PRAD, and THYM, but negatively associated with infiltration of CD8 T cells in HNSC, KIRC, KIRP and THYM. Moreover, ZNRF3 expression was correlated with most immune checkpoint genes in SARC, LUSC, LUAD, PRAD, THCA, UVM, TGCT, and OV, and associated with overwhelming majority of immunoregulatory genes in almost all cancers. Most RNA modification genes were also remarkably related to ZNRF3 level in KIRP, LUAD, LUSC, THYM, UVM, PRAD, and UCEC, indicating that ZNRF3 might have an important effect on cancer epigenetic regulation. Finally, we verified the expression and role of ZNRF3 in clinical specimens and cell lines of renal cancer and liver cancer. This study provides a comprehensive pan-cancer analysis of ZNRF3 and reveals the complexity of its carcinogenic effect. Zinc and ring finger 3 (ZNRF3) was significantly dysregulated in a variety of cancers. Aberrant expression of ZNRF3 was associated with poor prognosis in some cancers. ZNRF3 expression was related to the levels of copy number variation and DNA methylation. ZNRF3 expression were associated with tumor heterogeneity, tumor stemness, immune score, stromal score and ESTIMATE score in certain cancers. ZNRF3 expressions in KIRC and LIHC were determined by clinical specimens again. ZNRF3 roles in KIRC and LIHC were investigated in cell lines.image
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页数:19
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