» Articles » PMID: 32677169

Mechanism of Tumor-suppressive Cell Competition in Flies

Overview
Journal Cancer Sci
Specialty Oncology
Date 2020 Jul 18
PMID 32677169
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Oncogenic mutations often trigger antitumor cellular response such as induction of apoptosis or cellular senescence. Studies in the last decade have identified the presence of the third guardian against mutation-induced tumorigenesis, namely "cell competition." Cell competition is a context-dependent cell elimination whereby cells with higher fitness eliminate neighboring cells with lower fitness by inducing cell death. While oncogene-induced apoptosis or oncogene-induced senescence acts as a cell-autonomous tumor suppressor, cell competition protects the tissue from tumorigenesis via cell-cell communication. For instance, in Drosophila epithelium, oncogenic cells with cell polarity mutations overproliferate and develop into tumors on their own but are eliminated from the tissue when surrounded by wild-type cells. Genetic studies in flies have unraveled that such tumor-suppressive cell competition is regulated by at least three mechanisms: direct cell-cell interaction between polarity-deficient cells and wild-type cells, secreted factors from epithelial cells, and systemic factors from distant organs. Molecular manipulation of tumor-suppressive cell competition could provide a novel therapeutic strategy against human cancers.

Citing Articles

Flamingo participates in multiple models of cell competition.

Bosch P, Cho B, Axelrod J Elife. 2025; 13.

PMID: 39854621 PMC: 11684786. DOI: 10.7554/eLife.98535.


Coordination of tissue homeostasis and growth by the Scribble-α-Catenin-Septate junction complex.

Huang Y, Gui J, Myllymaki S, Mikkola M, Shimmi O iScience. 2023; 26(4):106490.

PMID: 37096043 PMC: 10122046. DOI: 10.1016/j.isci.2023.106490.


Sas-Ptp10D shapes germ-line stem cell niche by facilitating JNK-mediated apoptosis.

Taniguchi K, Igaki T PLoS Genet. 2023; 19(3):e1010684.

PMID: 36972315 PMC: 10079222. DOI: 10.1371/journal.pgen.1010684.


WASH activation controls endosomal recycling and EGFR and Hippo signaling during tumor-suppressive cell competition.

Liu D, Tsarouhas V, Samakovlis C Nat Commun. 2022; 13(1):6243.

PMID: 36271083 PMC: 9587002. DOI: 10.1038/s41467-022-34067-1.


Scribble and α-Catenin cooperatively regulate epithelial homeostasis and growth.

Huang Y, Gui J, Myllymaki S, Roy K, Tonissoo T, Mikkola M Front Cell Dev Biol. 2022; 10:912001.

PMID: 36211469 PMC: 9532510. DOI: 10.3389/fcell.2022.912001.


References
1.
Zhu H, Blake S, Kusuma F, Pearson R, Kang J, Chan K . Oncogene-induced senescence: From biology to therapy. Mech Ageing Dev. 2020; 187:111229. DOI: 10.1016/j.mad.2020.111229. View

2.
Doggett K, Grusche F, Richardson H, Brumby A . Loss of the Drosophila cell polarity regulator Scribbled promotes epithelial tissue overgrowth and cooperation with oncogenic Ras-Raf through impaired Hippo pathway signaling. BMC Dev Biol. 2011; 11:57. PMC: 3206446. DOI: 10.1186/1471-213X-11-57. View

3.
Igaki T, Pagliarini R, Xu T . Loss of cell polarity drives tumor growth and invasion through JNK activation in Drosophila. Curr Biol. 2006; 16(11):1139-46. DOI: 10.1016/j.cub.2006.04.042. View

4.
Ohsawa S, Vaughen J, Igaki T . Cell Extrusion: A Stress-Responsive Force for Good or Evil in Epithelial Homeostasis. Dev Cell. 2018; 44(3):284-296. PMC: 6207186. DOI: 10.1016/j.devcel.2018.01.009. View

5.
Norman M, Wisniewska K, Lawrenson K, Garcia-Miranda P, Tada M, Kajita M . Loss of Scribble causes cell competition in mammalian cells. J Cell Sci. 2012; 125(Pt 1):59-66. PMC: 3269023. DOI: 10.1242/jcs.085803. View