Citation

BibTex format

@article{Nguyen:2026:10.1073/pnas.2534053123,
author = {Nguyen, P-K and Froldi, F and McMullen, JPD and Southall, TD and Marshall, OJ and Cheng, LY},
doi = {10.1073/pnas.2534053123},
journal = {Proc Natl Acad Sci U S A},
title = {Chinmo defines the region-specific oncogenic competence in the Drosophila central nervous system.},
url = {http://dx.doi.org/10.1073/pnas.2534053123},
volume = {123},
year = {2026}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - While genetic mutations can promote hyperplastic growth, they do not always result in oncogenic outcomes. We and others have previously identified the transcription factors Nerfin-1 and Lola as inhibitors of dedifferentiation. Here, we investigate how the oncogenic potential of dedifferentiation varies across different neural lineages in the Drosophila central nervous system. We found that Nerfin-1 inactivation causes tumorigenic phenotypes in the central brain and the ventral nerve cord but not the optic lobes (OLs). In contrast, Lola inactivation leads to tumor overgrowth specifically in the OLs. We identify Chinmo, a temporal transcription factor, and its regulation by ecdysone signaling as key determinants of the oncogenic competence in different regions of the brain, influencing the tumorigenic outcome of dedifferentiation. This study provides a fundamental framework to understand how oncogenic competence arises beyond genetic mutations.
AU - Nguyen,P-K
AU - Froldi,F
AU - McMullen,JPD
AU - Southall,TD
AU - Marshall,OJ
AU - Cheng,LY
DO - 10.1073/pnas.2534053123
PY - 2026///
TI - Chinmo defines the region-specific oncogenic competence in the Drosophila central nervous system.
T2 - Proc Natl Acad Sci U S A
UR - http://dx.doi.org/10.1073/pnas.2534053123
UR - https://www.ncbi.nlm.nih.gov/pubmed/42160347
VL - 123
ER -

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