Evidence mapPaperPMID 40745138Full record

ReviewAdvances in experimental medicine and biology2025

Drosophila Intestine as a Model to Study Tumors.

Jiae Lee, Young V Kwon

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Jiae LeeDepartment of Biological Sciences, California State University Long Beach, Long Beach, CA, USA.
Young V KwonDepartment of Biochemistry, University of Washington, Seattle, WA, USA. ykwon7@uw.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Drosophila melanogaster intestine has emerged as a powerful model system for studying the fundamental mechanisms underlying cancer biology, including tumorigenesis, metastasis, and paraneoplastic syndromes such as cachexia. The key signaling pathways implicated in human colorectal cancers play similar roles in the Drosophila intestinal system. Dysregulation of these pathways in the Drosophila intestine leads to overproliferation of intestinal stem cells, loss of cell differentiation, and potential transdifferentiation, mirroring tumorigenic processes in humans. Recent research utilizing Drosophila intestinal tumor models has provided novel insights into how oncogenes and tumor suppressors contribute to the formation and progression of tumors. Models involving activation of oncogenes like mutant Ras and inhibition of tumor suppressors like APC have been instrumental in elucidating mechanisms of tumor cell dissemination, invasion, and collective migration. Furthermore, Drosophila intestinal tumors induce paraneoplastic syndromes such as cancer cachexia and paraneoplastic renal dysfunction, enabling the identification of novel tumor-derived wasting factors, some of which play similar roles in mammals. Thus, the insights gained from Drosophila intestinal tumor models not only deepen our understanding of fundamental cancer biology but also hold promise for informing the development of novel therapeutic strategies for human cancers.

Indexed as

Disease Models, AnimalDrosophila melanogasterIntestinal NeoplasmsIntestinesAnimalsHumansSignal TransductionCachexiaDrosophilaIntestineInvasionMigrationParaneoplastic syndromesStem cell differentiationTissue homeostasisTissue regenerationTumor cell disseminationTumorigenesis

Identifiers

What Socratic holds

Textmetadata
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 Socratic graph.