Evidence map›Paper›PMID 32394616›Full record

ArticleMolecular oncology2020

CD24 blunts the sensitivity of retinoblastoma to vincristine by modulating autophagy.

Jie Sun, Dongju Feng, Huiyu Xi, Jiajing Luo, Zewei Zhou, Qinghuai Liu, Yun Chen, Qing Shao

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. CD24 Regulates the Formation of Ectosomes in B Lymphocytes.Journal of extracellular vesicles · 2025
    Article
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  6. Review
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  11. Review
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  13. Review
  14. Article
  15. CD24: A Novel Target for Cancer Immunotherapy.Journal of personalized medicine · 2022
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

8 authors at 3 institutions in 1 country.

Jie SunDepartment of Ophthalmology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Dongju FengDepartment of Immunology, Key Laboratory of Immune Microenvironment and Disease, Nanjing Medical University, Nanjing, China.
Huiyu XiDepartment of Ophthalmology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Jiajing LuoDepartment of Immunology, Key Laboratory of Immune Microenvironment and Disease, Nanjing Medical University, Nanjing, China.
Zewei ZhouDepartment of Immunology, Key Laboratory of Immune Microenvironment and Disease, Nanjing Medical University, Nanjing, China.
Qinghuai LiuDepartment of Ophthalmology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Yun ChenDepartment of Immunology, Key Laboratory of Immune Microenvironment and Disease, Nanjing Medical University, Nanjing, China.ORCID 0000-0002-9854-8108
Qing ShaoDepartment of Ophthalmology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Nanjing Medical University · CNJiangsu Province Hospital · CNXuzhou Medical College · CN

Funding

National Natural Science Foundation of China 81672673National Natural Science Foundation of China 81772602National Natural Science Foundation of China 9174210027Qing Lan Project, Jiangsu Provincial Key Research Development Program of China BE2018750
6 · The paper itself

Abstract

Retinoblastoma (RB) is the most common childhood malignant intraocular tumor. The clinical efficacy of vincristine (VCR) in the treatment of RB is severely limited by drug resistance. Here, we found that CD24, a GPI-anchored protein, was overexpressed in human RB tissues and RB cell lines, and was associated with the sensitivity of RB cells in response to VCR therapy. We demonstrated that CD24 plays a critical role in impairing RB sensitivity to VCR via regulating autophagy. Mechanistically, CD24 recruits PTEN to the lipid raft domain and regulates the PTEN/AKT/mTORC1 pathway to activate autophagy. Lipid raft localization was essential for CD24 recruitment function. Collectively, our findings revealed a novel role of CD24 in regulating RB sensitivity to VCR and showed that CD24 is a potential target for improving chemotherapeutic sensitivity and RB patient outcomes.

Indexed as

AutophagyAnimalsAutophagosomesCD24 AntigenCell Line, TumorGene Expression ProfilingGene Expression Regulation, NeoplasticGlycosylphosphatidylinositolsHumansMaleMechanistic Target of Rapamycin Complex 1Membrane MicrodomainsMice, Inbred BALB CMice, NudeProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseCD24 AntigenGlycosylphosphatidylinositolsMechanistic Target of Rapamycin Complex 1Proto-Oncogene Proteins c-aktPTEN PhosphohydrolaseVincristineautophagyCD24lipid raftretinoblastomavincristine

Identifiers

PMID32394616
PMCPMC7400807
OpenAlexW3025811449

What OpenQuestion holds

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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.