Evidence map›Paper›PMID 36855091›Full record

ArticleBMC cancer2023

Comprehensive analysis of the role of ICOS ( CD278 ) in pan-cancer prognosis and immunotherapy.

Xiashuang Zhao, Yongfeng Wang, Xianglai Jiang, Bangqian Mo, Chenyu Wang, Mingzheng Tang, Yao Rong, Guiqian Zhang, Ming Hu, Hui Cai

Abstract read
In one paragraph

Article in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. ICOSL: more than a trigger of ICOS function.Cell communication and signaling : CCS · 2025
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
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

10 authors.

Xiashuang Zhao *The First Clinical Medical College of Gansu, University of Chinese Medicine (Gansu Provincial Hospital), 730000, Lanzhou, Gansu, China.
Yongfeng Wang *General Surgery Clinical Medical Center, Gansu Provincial Hospital, 730000, Lanzhou, Gansu, China.
Xianglai JiangGeneral Surgery Clinical Medical Center, Gansu Provincial Hospital, 730000, Lanzhou, Gansu, China.
Bangqian MoThe First Clinical Medical College of Gansu, University of Chinese Medicine (Gansu Provincial Hospital), 730000, Lanzhou, Gansu, China.
Chenyu WangGraduate School, Ning Xia Medical University, 750004, Yinchuan, Ningxia, China.
Mingzheng TangThe First Clinical Medical College of Gansu, University of Chinese Medicine (Gansu Provincial Hospital), 730000, Lanzhou, Gansu, China.
Yao RongThe First Clinical Medical College of Gansu, University of Chinese Medicine (Gansu Provincial Hospital), 730000, Lanzhou, Gansu, China.
Guiqian ZhangThe First Clinical Medical College of Gansu, University of Chinese Medicine (Gansu Provincial Hospital), 730000, Lanzhou, Gansu, China.
Ming HuGansu Provincial Hospital, 730000, Lanzhou, Gansu, China. 120220903131@lzu.edu.cn.ORCID http://orcid.org/0000-0002-6182-966X
Hui CaiGeneral Surgery Clinical Medical Center, Gansu Provincial Hospital, 730000, Lanzhou, Gansu, China. caialonteam@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe immunological checkpoint known as Inducible T Cell Costimulatory Factor (ICOS, Cluster of Differentiation, CD278) is activated and expressed on T cells. Both somatic cells and antigen-presenting cells expressed its ligand, ICOSL (including tumor cells in the tumor microenvironment).It is important for immunosuppression. Uncertainty surrounds the function of ICOS in tumor immunity.

methodsSeveral bioinformatics techniques were employed by us to thoroughly examine the expression and prognostic value of ICOS in 33 cancers based on data collected from TCGA and GTEx. In addition, ICOS was explored with pathological stage, tumor-infiltrating cells, immune checkpoint genes, mismatch repair (MMR) genes, DNA methyltransferases (DNMTs), microsatellite instability (MSI),and tumor mutation burden (TMB).In addition,To ascertain the level of ICOS expression in various cells, qRT-PCR was employed.

resultsThe findings revealed that ICOS expression was up regulation in most cancer types. The high expression of ICOS in tumor samples was related to the poor prognosis of UVM and LGG; The positive prognosis was boosted by the strong expression of ICOS in OV, SARC, SKCM, THYM, UCEC, and HNSC. The result is that the expression of malignancy was revealed by the immune cells' invasion.profile of ICOS in different types of cancer. Different ways that ICOS expression is connected to immune cell infiltration account for variations in patient survival. Additionally, the TMB, MSI, MMR, and DNMT genes as well as ICOS expression are linked in many cancer types.The results of PCR showed that it is highly expressed in gastric, breast, liver and renal cell carcinoma cell lines compared with normal cells.

conclusionThis study suggests that ICOS may be a potential tumor immunotherapy target and prognostic marker.

Indexed as

ImmunotherapyNeoplasmsAntigen-Presenting CellsBreastDNA Modification MethylasesHumansImmunosuppression TherapyInducible T-Cell Co-Stimulator ProteinLiverDNA Modification MethylasesICOS protein, humanInducible T-Cell Co-Stimulator ProteinICOSImmune checkpointPan-cancerPrognosisTumor immune

Identifiers

PMID36855091
PMCPMC9971684

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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.