Evidence map›Paper›PMID 30381753›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2018

Interleukin-22 Promotes Osteosarcoma Cell Proliferation and Invasion via STAT3 Activation.

Panpan Li, Xin Shi, Yonghui Xu, Binggang Zhong, Yu Lu, Yong Sun

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 24% 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, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. The role of IL-22 in cancer.Medical oncology (Northwood, London, England) · 2024
    Review
  4. Article
  5. Article
  6. Relationship between Th17 immune response and cancer.World journal of clinical oncology · 2021
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  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

6 authors at 2 institutions in 1 country.

Panpan LiDepartment of Radiology, The Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China (mainland).
Xin ShiDepartment of Traumatology, The Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China (mainland).
Yonghui XuDepartment of Radiology, The Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China (mainland).
Binggang ZhongDepartment of Orthopedics, The First People's Hospital of Zhao Tong, Zhaotong, Yunnan, China (mainland).
Yu LuDepartment of Orthopedics, The Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China (mainland).
Yong SunDepartment of Radiology, The Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China (mainland).
Kunming Medical University · CNZhaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Interleukin-22 (IL-22) is one of the cytokines secreted by T-helper 17 (Th17) cells. It belongs to the IL-10 cytokine family and influences a variety of immune reactions. Studies have indicated that IL-22 can promote cancer progression and metastases. However, the function of IL-22 in osteosarcoma (OS) remains unclear. MATERIAL AND METHODS In this study, the expression of IL-22 in the OS cell line was detected by qRT-PCR. The role of IL-22 in proliferation and invasion in OS cells was tested by MTT and Transwell assays. The protein expression of STAT3, phospho-STAT3, AKT, and phospho-AKT was detected by Western blot analysis. RESULTS The results showed that IL-22 was upregulated in OS cells. IL-22 dose-independently promoted OS cells proliferation and invasion, which could be reversed by IL-22 antibody or STAT3 siRNA. Furthermore, IL-22 exposure of OS cells resulted in dose-independently increased levels of phosphorylated STAT3 protein kinases. Interestingly, IL-22 did not influence the expression of phosphorylated AKT. CONCLUSIONS These results suggest that IL-22 promotes OS cells proliferation and invasion and its effect is mediated by activation of the STAT3 pathway. These findings demonstrate that IL-22 may serve as a promising molecular biomarker for diagnosis and therapy for OS patients.

Indexed as

Bone NeoplasmsCell Line, TumorCell ProliferationCytokinesHumansInterleukin-22InterleukinsNeoplasm InvasivenessOsteosarcomaPhosphorylationProto-Oncogene Proteins c-aktSignal TransductionSTAT3 Transcription FactorTh17 CellsCytokinesInterleukin-22InterleukinsProto-Oncogene Proteins c-aktSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID30381753
PMCPMC6225732
OpenAlexW2898763194

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.