Evidence map›Paper›PMID 34220863›Full record

ArticleFrontiers in immunology2021

RPL22 Overexpression Promotes Psoriasis-Like Lesion by Inducing Keratinocytes Abnormal Biological Behavior.

Jinrong Zeng, Yue Zhang, Hanyi Zhang, Yuezhong Zhang, Lihua Gao, Xiaoliang Tong, Yajie Xie, Qian Hu, Chunli Chen, Shu Ding and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. CEACAM5 drives psoriatic inflammation by regulating CD8Biochemistry and biophysics reports · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. 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

11 authors at 2 institutions in 1 country.

Jinrong ZengDepartment of Dermatology, Third Xiangya Hospital, Central South University, Changsha, China.
Yue ZhangXiangYa School of Medicine, Central South University, Changsha, China.
Hanyi ZhangXiangYa School of Medicine, Central South University, Changsha, China.
Yuezhong ZhangXiangYa School of Medicine, Central South University, Changsha, China.
Lihua GaoDepartment of Dermatology, Third Xiangya Hospital, Central South University, Changsha, China.
Xiaoliang TongDepartment of Dermatology, Third Xiangya Hospital, Central South University, Changsha, China.
Yajie XieDepartment of Dermatology, Third Xiangya Hospital, Central South University, Changsha, China.
Qian HuDepartment of Dermatology, Third Xiangya Hospital, Central South University, Changsha, China.
Chunli ChenDepartment of Dermatology, Third Xiangya Hospital, Central South University, Changsha, China.
Shu DingDepartment of Dermatology, Third Xiangya Hospital, Central South University, Changsha, China.
Jianyun LuDepartment of Dermatology, Third Xiangya Hospital, Central South University, Changsha, China.
Central South University · CNThird Xiangya Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Keratinocytes of psoriasis have anti-apoptotic properties including delayed apoptosis process, accelerated proliferation metabolism and postponed differentiation process. However, the specific mechanism leading to the abnormal biological behavior of keratinocytes remains unclear. Objectives: We investigated the role of increased RPL22 expression in regulating the abnormal biological behavior of keratinocytes and the mechanism of regulation of RPL22 expression in skin lesions of psoriatic patients. Methods: We examined clinical samples and utilized cytokine-induced cell and IMQ-treated mouse models. We determined the expression and functions of RPL22 Results: We showed that RPL22 expression was significantly increased in the skin lesions of psoriasis patients and IMQ-treated psoriatic-like mice. Such increased expression is attributed to hyperacetylation of histone H3K27 in the promoter region of RPL22. Interestingly, overexpression of RPL22 enhanced keratinocyte proliferation by increasing cyclinD1 expression and accelerated CD4 Conclusions: These findings suggested that RPL22 regulates keratinocytes abnormal biological behavior and contributes to the development of psoriatic phenotypes. Thus, RPL22 might be a novel potential molecular target for treatment of psoriasis.

Indexed as

AnimalsFemaleHumansKeratinocytesMiceMice, Inbred BALB CPsoriasisRibosomal ProteinsRNA-Binding ProteinsUp-RegulationRibosomal ProteinsRNA-Binding ProteinsRPL22 protein, humanCXCL10CyclinD1H3K27ackeratinocytespsoriasisRPL22

Identifiers

PMID34220863
PMCPMC8250439
OpenAlexW3174601512

What OpenQuestion holds

Textmetadata
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.