Elimination of oncogenic neighbors by JNK-mediated engulfment in Drosophila
Open accessAbstract
A newly emerged oncogenic cell in the epithelial population has to confront antitumor selective pressures in the host tissue. However, the mechanisms by which surrounding normal tissue exerts antitumor effects against oncogenically transformed cells are poorly understood. In Drosophila imaginal epithelia, clones of cells mutant for evolutionarily conserved tumor suppressor genes such as scrib or dlg lose their epithelial integrity and are eliminated from epithelia when surrounded by wild-type tissue. Here, we show that surrounding normal cells activate nonapoptotic JNK signaling in response to the emergence of oncogenic mutant cells. This JNK activation leads to upregulation of PVR, the Drosophila PDGF/VEGF receptor. Genetic and time-lapse imaging analyses reveal that PVR expression in surrounding cells activates the ELMO/Mbc-mediated phagocytic pathway, thereby eliminating oncogenic neighbors by engulfment. Our data indicate that JNK-mediated cell engulfment could be an evolutionarily conserved intrinsic tumor-suppression mechanism that eliminates premalignant cells from epithelia.
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Nonautonomous JNK signaling promotes wild-type neighbors to engulf scribble mutant cells.
“In contrast, nonautonomous JNK signaling promotes wild-type neighbors to engulf scribble mutant cells (Ohsawa et al., 2011).”
From Scribble: A master scaffold in polarity, adhesion, synaptogenesis, and proliferation (2019) · cites this paper as Ohsawa et al., 2011
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References 77 · Cited by 200
- Authors
- Ohsawa, S., Sugimura, K., Takino, K., Xu, T., Miyawaki, A., & Igaki, T.
- Affiliations
- Kobe University (JP)
- RIKEN Center for Brain Science (JP)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Igaki, Tatsushi
- Venue
- Developmental Cell
- Publisher
- Elsevier BV
- Published
- 2011-03
- Volume
- 20
- Issue
- 3
- Pages
- 315-328
- ISSN
- 1534-5807 (ISSN-L)
- OpenAlex
- W1993790646
- Cited by
- 200
- References
- 77
- Citations by year
- 2026: 3 · 2025: 12 · 2024: 10 · 2023: 11 · 2022: 10 · 2021: 9 · 2020: 10 · 2019: 13 · 2018: 19 · 2017: 17 · 2016: 10 · 2015: 13 · 2014: 17 · 2013: 17 · 2012: 20
- FWCI
- 8.90
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1360 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Developmental Cell (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Fumi Yamamura Memorial Foundation for Female Natural Scientists
- Human Frontier Science Program
- RIKEN
- Japan Society for the Promotion of Science
- Astellas Foundation for Research on Metabolic Disorders
- Senri Life Science Foundation
- Sumitomo Foundation
- Kanae Foundation for the Promotion of Medical Science
- Ministry of Education, Culture, Sports, Science and Technology
- NOVARTIS Foundation (Japan) for the Promotion of Science
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Invertebrate Immune Response Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Keywords
- tumor suppression, JNK signaling, cell engulfment, phagocytosis, SCRIB, Dlg, premalignant cells, Drosophila
- MeSH terms
- Animals, Drosophila melanogaster, Enzyme Activation, Epithelium, Membrane Proteins, Neoplasms, Oncogenes, Phagocytosis, Recombinant Fusion Proteins, Signal Transduction, Receptor Protein-Tyrosine Kinases, Tumor Suppressor Proteins, Drosophila Proteins, JNK Mitogen-Activated Protein Kinases, Adaptor Proteins, Signal Transducing
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