Evidence map›Paper›PMID 34804789›Full record

ArticleJournal of bone oncology2021

Interleukin-24 inhibits the phenotype and tumorigenicity of cancer stem cell in osteosarcoma via downregulation Notch and Wnt/β-catenin signaling.

Baobiao Zhuo, Xihua Wang, Yang Shen, Jiayong Li, Shixian Li, Yuan Li, Rong Wang

Open access · goldAbstract read
In one paragraph

Article in Journal of bone oncology, 2021. 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
1.0field-weighted citation impact, top 21% 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, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. NOTCH Signaling in Osteosarcoma.Current issues in molecular biology · 2023
    Review
  11. Interleukin gene delivery for cancer gene therapy:Iranian journal of basic medical sciences · 2023
    Review
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

7 authors at 1 institution in 1 country.

Baobiao ZhuoDepartment of Surgery, Affiliated Xuzhou Children's Hospital of Xuzhou Medical University, 221002 Xuzhou, Jiangsu, China.
Xihua WangDepartment of Surgery, Affiliated Xuzhou Children's Hospital of Xuzhou Medical University, 221002 Xuzhou, Jiangsu, China.
Yang ShenDepartment of Surgery, Affiliated Xuzhou Children's Hospital of Xuzhou Medical University, 221002 Xuzhou, Jiangsu, China.
Jiayong LiDepartment of Surgery, Affiliated Xuzhou Children's Hospital of Xuzhou Medical University, 221002 Xuzhou, Jiangsu, China.
Shixian LiDepartment of Surgery, Affiliated Xuzhou Children's Hospital of Xuzhou Medical University, 221002 Xuzhou, Jiangsu, China.
Yuan LiDepartment of Surgery, Affiliated Xuzhou Children's Hospital of Xuzhou Medical University, 221002 Xuzhou, Jiangsu, China.
Rong WangDepartment of Ultrasound, The Affiliated Hospital of Xuzhou Medical University, 221006 Xuzhou, Jiangsu, China.
Xuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma frequently presents as recurrence and metastasis, even if the primary lesion was eradicated and/or radiotherapy and chemotherapy were administered. Osteosarcoma cancer stem cells (CSCs) are one of the key factors for the recurrence and metastasis of osteosarcoma. We have shown that interleukin-24 (IL-24) inhibits osteosarcoma cell proliferation, migration and invasion in vitro. In the current study, we investigated the role of IL-24 in inhibiting the growth of osteosarcoma CSCs. IL-24 inhibited proliferation and invasion and decreased the stemness of osteosarcoma CSCs in vitro. In a nude mouse xenograft model, IL-24 significantly inhibited the growth of tumors originating from osteosarcoma CSCs. Moreover, we found that IL-24 was able to inactivate both Notch and Wnt/β-Catenin signaling, which are important for the development of the biological characteristics of CSCs. These data demonstrate that IL-24 is able to kill not only cancer cells but also CSCs in osteosarcoma, suggesting that IL-24 might eradicate osteosarcoma and enhance long-term cure rates in patients with osteosarcoma.

Indexed as

bFGF, basic fibroblast growth factorCancer stem cellCSCs, cancer stem cellsEGF, Epidermal Growth FactorHDAC6, histone deacetylase 6IL-24IL-24, interleukin-24JNK, c-Jun N-terminal kinase (JNKMTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTTNotch signalingNS, nucleosteminOsteosarcomaWnt/β-catenin signaling

Identifiers

PMID34804789
PMCPMC8581362
OpenAlexW3209431566

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.