Evidence map›Paper›PMID 34730289›Full record

ReviewWIREs mechanisms of disease2021

Tumor models in various Drosophila tissues.

Shangyu Gong, Yichi Zhang, Aiguo Tian, Wu-Min Deng

Abstract readReview
In one paragraph

Review in WIREs mechanisms of disease, 2021. 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
–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

24 citing papers in PubMed.

  1. Biology · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Deciphering Ultra-High Dose Rate Irradiation withAntioxidants (Basel, Switzerland) · 2026
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Drosophila as a Model for Metastasis.Advances in experimental medicine and biology · 2025
    Review
  12. Article
  13. Epigenetic Regulation in Drosophila Tumor Models.Advances in experimental medicine and biology · 2025
    Review
  14. Notch Signaling in Drosophila Tumor Models.Advances in experimental medicine and biology · 2025
    Review
  15. Article
  16. Growth deregulation and interaction with host hemocytes contribute to tumor progression in a Drosophila brain tumor model.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  17. Article
  18. Article
  19. Review
  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

4 authors.

Shangyu GongDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, Louisiana, USA.ORCID 0000-0002-6799-982X
Yichi ZhangDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, Louisiana, USA.ORCID 0000-0002-1780-7156
Aiguo TianDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, Louisiana, USA.ORCID 0000-0001-5011-6034
Wu-Min DengDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, Louisiana, USA.ORCID 0000-0002-9098-9769

Funding

The role of the CMV-associated reactive oxygen species in age-relatedP20GM103629 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI TIAN, AIGUO · 2012 to 2021
$22.4M
Notch signaling and germline-soma interactions in the Drosophila ovarian modelR01GM072562 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI DENG, WU-MIN · 2006 to 2025
$5.6M
Tissue Microenvironment ant Tumor Hotspots in DrosophilaR01CA227789 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI DENG, WU-MIN · 2019 to 2023
$1.7M
Mechanistic investigation of malignant rhabdoid childhood tumor using the Drosophila modelR01CA224381 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI DENG, WU-MIN · 2018 to 2022
$1.7M
NCI NIH HHS R01 CA224381NCI NIH HHS R01 CA227789NIGMS NIH HHS P20 GM103629NIGMS NIH HHS R01 GM072562
6 · The paper itself

Abstract

The development of cancer is a complex multistage process. Over the past few decades, the model organism Drosophila melanogaster has been crucial in identifying cancer-related genes and pathways and elucidating mechanisms underlying growth regulation in development. Investigations using Drosophila has yielded new insights into the molecular mechanisms involved in tumor initiation and progression. In this review, we describe various tumor models that have been developed in recent years using different Drosophila tissues, such as the imaginal tissue, the neural tissue, the gut, the ovary, and hematopoietic cells. We discuss underlying genetic alterations, cancer-like characteristics, as well as similarities and key differences among these models. We also discuss how disruptions in stem cell division and differentiation result in tumor formation in diverse tissues, and highlight new concepts developed using the fly model to understand context-dependent tumorigenesis. We further discuss the progress made in Drosophila to explore tumor-host interactions that involve the innate immune response to tumor growth and the cachexia wasting phenotype. This article is categorized under: Cancer > Genetics/Genomics/Epigenetics Cancer > Stem Cells and Development Cancer > Molecular and Cellular Physiology.

Indexed as

DrosophilaNeoplasmsAnimalsCachexiaCell DifferentiationDrosophila melanogasterFemalecachexiacancerDrosophilastem celltumor

Identifiers

PMID34730289
PMCPMC8566734

What OpenQuestion holds

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Registered trials

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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.