Evidence map›Paper›PMID 36822671›Full record

ArticleJournal for immunotherapy of cancer2023

ANKRD22 is a potential novel target for reversing the immunosuppressive effects of PMN-MDSCs in ovarian cancer.

Huanhuan Chen, Keqing Yang, Lingxiao Pang, Jing Fei, Yongliang Zhu, Jianwei Zhou

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Trial
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  3. Review
  4. PVNJournal of neuroinflammation · 2026
    Article
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  6. Article
  7. Article
  8. Review
  9. Article
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  11. Article
  12. Downregulation ofTranslational cancer research · 2025
    Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
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  20. 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

6 authors.

Huanhuan Chen *Second affiliated hospital, Zhejiang University School of Medicine, Hangzhou, China.
Keqing Yang *Second affiliated hospital, Zhejiang University School of Medicine, Hangzhou, China.
Lingxiao PangSecond affiliated hospital, Zhejiang University School of Medicine, Hangzhou, China.
Jing FeiSecond affiliated hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yongliang ZhuSecond affiliated hospital, Zhejiang University School of Medicine, Hangzhou, China ylzhu@zju.edu.cn 2195045@zju.edu.cn.ORCID 0000-0001-7450-885X
Jianwei ZhouSecond affiliated hospital, Zhejiang University School of Medicine, Hangzhou, China ylzhu@zju.edu.cn 2195045@zju.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOvarian cancer is the deadliest type of malignant gynecological tumor. Polymorphonuclear myeloid-derived suppressor cells (PMN-MDSCs) are involved ovarian cancer and are closely related to adverse outcomes. However, the immunosuppressive mechanism of PMN-MDSCs remains elusive.

methodsThe types and numbers of ANKRD22-expressing cells were investigated by bioinformatics analysis and immunohistochemical staining.

resultsWe identified a novel protein involved in regulating the immunosuppressive ability of PMN-MDSCs, ANKRD22.

conclusionsThese results suggest that ANKRD22 is a potential novel target for reversing the immunosuppressive effects of PMN-MDSCs.

Indexed as

Myeloid-Derived Suppressor CellsOvarian NeoplasmsAnimalsFemaleHLA-DR AntigensHumansImmunosuppressive AgentsMiceMice, Inbred C57BLMice, KnockoutHLA-DR AntigensImmunosuppressive AgentsMyeloid-Derived Suppressor CellsTumor Microenvironment

Identifiers

PMID36822671
PMCPMC9950970

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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.