Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Cancer Cell Migration through Invadopodia01:35

Cancer Cell Migration through Invadopodia

Invadosome is a broad category of cell surface structures with proteolytic activity that  degrades the extracellular matrix (ECM). Invadosomes are present in normal cell types, including macrophages, endothelial cells, and neurons, as well as tumor cells. Although the macrophage podosomes and tumor cell invadopodia are classified as invadosomes, they have different structures, molecular pathways, and functions. Podosomes are short structures that last for a few minutes. However, invadopodia can...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

A novel COE-D8-fosfomycin conjugate effectively combats first-line antibiotic-resistant uropathogenic Escherichia coli.

PloS one·2026
Same author

Ferroptosis as a therapeutic vulnerability in ARID1A-deficient bladder cancer.

Communications biology·2026
Same author

miRNA-7145-cuedc2 axis controls hematopoiesis through JAK1/STAT3 signaling pathway.

Cell death discovery·2024
Same author

Development of a stemness-related prognostic index to provide therapeutic strategies for bladder cancer.

NPJ precision oncology·2024
Same author

The spatiotemporal dynamics of spatially variable genes in developing mouse brain revealed by a novel computational scheme.

Cell death discovery·2023
Same author

Effect of mirror use on lower extremity muscle strength of patients with chronic stroke.

Journal of physical therapy science·2018

Related Experiment Video

Updated: Jun 10, 2026

3-D Cell Culture System for Studying Invasion and Evaluating Therapeutics in Bladder Cancer
09:24

3-D Cell Culture System for Studying Invasion and Evaluating Therapeutics in Bladder Cancer

Published on: September 13, 2018

EP300 promotes bladder cancer cell migration through SNAI2.

Qing Zhang1,2, Chongjie He1, Yingzhou Hong1

  • 1Yunnan Key Laboratory of Cell Metabolism and Disease, Center for Life Sciences, School of Life Sciences, Yunnan University, Kunming, China.

Plos One
|June 8, 2026
PubMed
Summary

EP300 promotes bladder cancer invasion by upregulating SNAI2. Targeting EP300 with A485 inhibits cancer cell migration and invasion, suggesting a potential therapeutic strategy for bladder cancer.

More Related Videos

A Murine Orthotopic Bladder Tumor Model and Tumor Detection System
06:23

A Murine Orthotopic Bladder Tumor Model and Tumor Detection System

Published on: January 12, 2017

Related Experiment Videos

Last Updated: Jun 10, 2026

3-D Cell Culture System for Studying Invasion and Evaluating Therapeutics in Bladder Cancer
09:24

3-D Cell Culture System for Studying Invasion and Evaluating Therapeutics in Bladder Cancer

Published on: September 13, 2018

A Murine Orthotopic Bladder Tumor Model and Tumor Detection System
06:23

A Murine Orthotopic Bladder Tumor Model and Tumor Detection System

Published on: January 12, 2017

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Research

Background:

  • EP300, a transcriptional coactivator, is frequently mutated in bladder cancer and correlates with malignancy.
  • Muscle-invasive progression in aggressive bladder cancers is linked to epithelial-mesenchymal transition (EMT).

Purpose of the Study:

  • To validate the association between EP300 and bladder cancer malignancy.
  • To investigate the therapeutic potential of EP300 inhibition using A485 in bladder cancer models.

Main Methods:

  • Immunohistochemical staining of bladder cancer tissues.
  • In vitro assays (scratch wound healing, Transwell) using bladder cancer cell lines (SW780, T24, RT4, 5637).
  • 3D organoid culture, in vivo mouse models, Bulk RNAseq, and Western blotting.

Main Results:

  • A485 significantly inhibited bladder cancer cell migration and disrupted organoid structures.
  • A485 showed a trend toward inhibiting in vivo bladder cancer invasion.
  • A485 downregulated SNAI2 signaling and reduced H3K27ac levels, while SNAI2 overexpression enhanced cell migration.

Conclusions:

  • EP300 promotes bladder cancer cell migration and invasion by upregulating SNAI2.
  • Targeting EP300 with A485 is a potential therapeutic strategy to inhibit bladder cancer invasion.