TRIM29 promotes bladder cancer invasion by regulating the intermediate filament network and focal adhesion

Bladder cancer is a common malignancy whose lethality is determined by invasive potential. We have previously shown that TRIM29, also known as ATDC, is transcriptionally regulated by TP63 in basal bladder cancers where it promotes invasive progression and metastasis, but the molecular events which promote invasion and metastasis downstream of TRIM29 remained poorly understood. Here we identify stimulation of bladder cancer migration as the specific role of TRIM29 during invasion. We show that TRIM29 physically interacts with K14+ intermediate filaments which, in turn, regulates focal adhesion stability. Further, we find that both K14 and the focal adhesion protein, ZYX are required for bladder cancer migration and invasion. Taken together, these results establish a role for TRIM29 in the regulation of cytoskeleton and focal adhesions during invasion and identify a pathway with therapeutic potential.

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Publication Details

Journal
Oncogene
Published
2025-09-04
DOI
https://doi.org/10.1038/s41388-025-03557-z
Citations
1
Primary Topic
Bladder and Urothelial Cancer Treatments
Type
article
Field-Weighted Citation Impact
2.01

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article

TRIM29 promotes bladder cancer invasion by regulating the intermediate filament network and focal adhesion

Marian L. Henderson, Alan Kelleher, Mark L. Day, Nicole A. Jerome et al.
1 citations
Oncogene
Bladder and Urothelial Cancer Treatments
2.01
article

TRIM29 promotes bladder cancer invasion by regulating the intermediate filament network and focal adhesion

Marian L. Henderson, Alan Kelleher, Mark L. Day, Nicole A. Jerome, Pierre A. Coulombe, Phillip L. Palmbos, Yin Wang
article en
1 citations

Abstract

Bladder cancer is a common malignancy whose lethality is determined by invasive potential. We have previously shown that TRIM29, also known as ATDC, is transcriptionally regulated by TP63 in basal bladder cancers where it promotes invasive progression and metastasis, but the molecular events which promote invasion and metastasis downstream of TRIM29 remained poorly understood. Here we identify stimulation of bladder cancer migration as the specific role of TRIM29 during invasion. We show that TRIM29 physically interacts with K14+ intermediate filaments which, in turn, regulates focal adhesion stability. Further, we find that both K14 and the focal adhesion protein, ZYX are required for bladder cancer migration and invasion. Taken together, these results establish a role for TRIM29 in the regulation of cytoskeleton and focal adhesions during invasion and identify a pathway with therapeutic potential.

OncogeneVol. 44(42)
University of Michigan (US), Michigan Medicine (US)
Damon Runyon Cancer Research Foundation, Bladder Cancer Advocacy Network, National Institutes of Health, National Cancer Institute, National Institute of Arthritis and Musculoskeletal and Skin Diseases
Openalex Percentile: Top 12%
Bladder and Urothelial Cancer Treatments
2.01
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TRIM29 promotes bladder cancer invasion by regulating the intermediate filament network and focal adhesion — Marian L. Henderson, Alan Kelleher, et al. · Oncogene (2025) | TGRS Research Map | TGRS