Evidence map›Paper›PMID 36187930›Full record

ArticleComputational and structural biotechnology journal2022

Comprehensive analysis of tumor necrosis factor-α-inducible protein 8-like 2 (TIPE2): A potential novel pan-cancer immune checkpoint.

Kun-Hao Bai, Yi-Yang Zhang, Xue-Ping Li, Xiao-Peng Tian, Meng-Meng Pan, Da-Wei Wang, Yu-Jun Dai

Abstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Kun-Hao BaiState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, 651 Dongfeng East Road, Guangzhou 500020, Guangdong, China.
Yi-Yang ZhangState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, 651 Dongfeng East Road, Guangzhou 500020, Guangdong, China.
Xue-Ping LiState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, 651 Dongfeng East Road, Guangzhou 500020, Guangdong, China.
Xiao-Peng TianJiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou 215006, Jiangsu, China.
Meng-Meng PanNational Research Center for Translational Medicine, Ruijin Hospital affiliated to Shanghai Jiao Tong University School of Medicine, 197, Ruijin Road II, Shanghai 200025, China.
Da-Wei WangNational Research Center for Translational Medicine, Ruijin Hospital affiliated to Shanghai Jiao Tong University School of Medicine, 197, Ruijin Road II, Shanghai 200025, China.
Yu-Jun DaiState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, 651 Dongfeng East Road, Guangzhou 500020, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor necrosis factor-α-inducible protein 8-like 2 (TIPE2) is encoded by TNFAIP8L2 and is a newly identified negative regulator of natural and acquired immunity that plays a critical function in maintaining immune homeostasis. Recently, CAR-NK immune cell therapy has been a focus of major research efforts as a novel cancer therapeutic strategy. TIPE2 is a potential checkpoint molecule for immune cell maturation and antitumor immunity that could be used as a novel NK cell-based immunotherapeutic approach. In this study, we explored the expression of TNFAIP8L2 across various tumor types and found that TNFAIP8L2 was highly expressed in most tumor types and correlated with prognosis. Survival analysis showed that TNFAIP8L2 expression was predictive of improved survival in cervical-squamous-cell-carcinoma (CESC), sarcoma (SARC) and skin-cutaneous-melanoma (SKCM). Conversely, TNFAIP8L2 expression predicted poorer survival in acute myeloid leukemia (LAML), lower-grade-glioma (LGG), kidney-renal-clear-cell-carcinoma (KIRC) and uveal-melanoma (UVM). Analysis of stemness features and immune cell infiltration indicated that TNFAIP8L2 was significantly associated with cancer stem cell index and increased macrophage and dendritic cell infiltration. Our data suggest that TNFAIP8L2 may be a novel immune checkpoint biomarker across different tumor types, particularly in LAML, LGG, KIRC and UVM, and may have further utility as a potential target for immunotherapy.

Indexed as

BLCA, Bladder Urothelial CarcinomaBRCA, Breast invasive carcinomaCESC, Cervical squamous cell carcinoma and endocervical adenocarcinomaCHOL, CholangiocarcinomaCOAD, Colon adenocarcinomaESCA, Esophageal carcinomaGBM, Glioblastoma multiformeHNSC, Head and Neck squamous cell carcinomaImmune cell infiltrationKICH, Kidney ChromophobeKIRC, Kidney renal clear cell carcinomaKIRP, Kidney renal papillary cell carcinomaLAML, Acute Myeloid LeukemiaLGG, Lower Grade GliomaLIHC, Liver hepatocellular carcinomaLUAD, Lung adenocarcinomaLUSC, Lung squamous cell carcinomaMESO, MesotheliomaNew immune checkpointOV, Ovarian serous cystadenocarcinomaPAAD, Pancreatic adenocarcinomaPan-cancerPCPG, Pheochromocytoma and ParagangliomaPRAD, Prostate adenocarcinomaREAD, Rectum adenocarcinomaSARC, SarcomaSKCM, Skin Cutaneous MelanomaSTAD, Stomach adenocarcinomaStemness featureTGCT, Testicular Germ Cell TumorTHCA, Thyroid carcinomaTHYM, ThymomaTIPE2UCEC, Uterine Corpus Endometrial CarcinomaUCS, Uterine CarcinosarcomaUVM, Uveal Melanoma

Identifiers

PMID36187930
PMCPMC9508481

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.