Increased expression of IFI16 predicts adverse prognosis in multiple myeloma

被引:3
作者
Huang, Wenhui [1 ,2 ,3 ]
Qian, Tingting [1 ,2 ,3 ]
Huang, Zeyong [1 ,2 ,3 ]
Liu, Yan [4 ,5 ]
Cui, Longzhen [4 ,5 ]
Zhu, Pei [1 ,2 ,3 ]
Zhong, Qingfu [1 ,2 ,3 ]
Zeng, Tiansheng [1 ,2 ,3 ]
Fu, Lin [1 ,2 ,3 ,4 ,5 ]
Si, Chaozeng [6 ]
Deng, Cong [7 ]
机构
[1] Guangzhou Med Univ, Affiliated Hosp 2, Dept Hematol, Guangzhou, Peoples R China
[2] Guangzhou Med Univ, Affiliated Hosp 2, Translat Med Ctr, State Key Lab Resp Dis, Guangzhou, Peoples R China
[3] Guangzhou Med Univ, Affiliated Hosp 2, Guangdong Prov Educ Dept, Key Lab Nanoimmunoregulat Tumor Microenvironm Tum, Guangzhou, Peoples R China
[4] Henan Univ, Huaihe Hosp, Translat Med Ctr, Kaifeng, Peoples R China
[5] Henan Univ, Huaihe Hosp, Dept Hematol, Kaifeng, Peoples R China
[6] China Japan Friendship Hosp, Informat Ctr, Beijing, Peoples R China
[7] Guangzhou Med Univ, Affiliated Hosp 2, Dept Clin Lab, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
D O I
10.1038/s41397-021-00230-y
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Multiple myeloma (MM) is a malignancy of terminally differentiated plasma cells and does not have sufficient prognostic indicators. Interferon gamma inducible protein 16 (IFI16) plays a crucial role in B-cell differentiation. Several studies have shown that IFI16 predicted prognosis in many cancers. However, the relationship between MM prognosis and IFI16 expression has not been studied. In our study, we analyzed the prognostic role of IFI16 expression and explored the possible mechanism in MM progression by using 4498 myeloma patients and 52 healthy donors from 13 independent gene expression omnibus (GEO) datasets. The IFI16 expression increased with myeloma progression, ISS stage, 1q21 amplification, and relapse (all P < 0.01). MM patients with higher IFI16 expression had shorter survival in six datasets (all P < 0.05). Furthermore, multivariate analysis indicated that enhanced IFI16 expression was an independent poor prognostic factor for EFS and OS (P = 0.007, 0.009, respectively). And PPI, GO, KEGG, and GSEA also confirmed that IFI16 promoted MM progression by participating in tumor-related pathways. In conclusion, our study confirmed that IFI16 was a poor prognostic biomarker in MM.
引用
收藏
页码:520 / 532
页数:13
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