Evidence map›Paper›PMID 35634441›Full record

ArticleDisease markers2022

Comprehensive Analysis of RELL2 as a Potential Biomarker Associated with Tumor Immune Infiltrating Cells in a Pan-Cancer Analysis.

Kadeerjiang Musha, Xinqi Ge, Nuraliya Ablikim, Bing Lu, Chen Chen, Jianfei Huang

Open access · hybridAbstract read
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Article in Disease markers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 37% of its field
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

7 citing papers in PubMed, 7 citations in OpenAlex.

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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

6 authors at 3 institutions in 1 country.

Kadeerjiang MushaDepartment of Cardiothoracic Surgery, People's Hospital of Kizilsu Kirgiz Autonomous Prefecture, Kizilsu Kirgiz, 845350 Xinjiang, China.
Xinqi GeDepartment of Clinical Biobank & Institute of Oncology, Affiliated Hospital of Nantong University, Nantong, 226001 Jiangsu, China.ORCID https://orcid.org/0000-0003-3200-4551
Nuraliya AblikimTranslational Medicine Center, People's Hospital of Kizilsu Kirgiz Autonomous Prefecture, Kizilsu Kirgiz, 845350 Xinjiang, China.
Bing LuDepartment of Clinical Biobank & Institute of Oncology, Affiliated Hospital of Nantong University, Nantong, 226001 Jiangsu, China.
Chen ChenDepartment of Oncology, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing 210000, China.ORCID https://orcid.org/0000-0002-5132-2208
Jianfei HuangDepartment of Clinical Biobank & Institute of Oncology, Affiliated Hospital of Nantong University, Nantong, 226001 Jiangsu, China.ORCID https://orcid.org/0000-0002-1276-5962
Nantong University · CNNanjing Drum Tower Hospital · CNPeople's Hospital of Xinjiang Uygur Autonomous Region · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Receptor expressed in lymphoid tissues-like 2 (RELL2), which is a member of RELT family, is closely associated with the plasma membrane and acts as a modulator for RELT signaling. Overexpression of RELL2 induces the activation of MAPK14/p38 cascade and apoptosis. However, whether RELL2 contributes to cancers remains unclear. Here, we examined its role in cancer patient prognosis and various tumors. Methods: We used several bioinformatics methods, specifically gene set enrichment analysis (GSEA), ScanNeo, and ESTIMATE, to analyze the CCLE dataset, GTEx dataset, and TCGA dataset. We investigated the possible association of RELL2 with the microsatellite instability (MSI) of various tumors, tumor mutational burden (TMB), immune checkpoint, immune neoantigens, immune microenvironment, and patient prognosis. Result: RELL2 is highly expressed in cancer compared with normal tissues. RELL2 expression is linked with worse progression-free interval and overall survival in numerous cancers. In most cancers, high RELL2 expression was related to a poor prognosis. RELL2 expression was significantly associated with the tumor microenvironment, MSI, and TMB. RELL2 expression is strongly associated with phenotypes that are of major clinical significance, particularly those associated with immune neoantigens and the expression profiles of immune checkpoint genes in pan-cancer. RELL2 expression strongly linked with the expressions of methyltransferases and DNA repair genes. It also significantly correlated with multiple signaling pathways through gene set enrichment analysis. Conclusion: RELL2 may be a prognostic biomarker in pan-cancer and may have an important function in tumorigenesis and progression.

Indexed as

NeoplasmsBiomarkers, TumorCarrier ProteinsHumansLymphoid TissueMembrane ProteinsMicrosatellite InstabilityMutationTumor MicroenvironmentBiomarkers, TumorCarrier ProteinsMembrane ProteinsRELL2 protein, human

Identifiers

PMID35634441
PMCPMC9132657
OpenAlexW4280490305

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Registered trials

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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.