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Updated: Apr 20, 2026

In vitro Organoid Culture of Primary Mouse Colon Tumors
Published on: May 17, 2013
Role of the focal adhesion protein TRIM15 in colon cancer development
Ok-Hee Lee1, Jinkyoung Lee2, Keun Ho Lee2
1Department of Biomedical Science, CHA University, Seongnam-si, Gyeonggi-do, Republic of Korea; Severance Integrative Research Institute for Cerebral and Cardiovascular Diseases, Yonsei University Health System, Seoul, Republic of Korea.
Abstract:
The tripartite motif containing (TRIM) proteins are a large family of proteins that have been implicated in many biological processes including cell differentiation, apoptosis, transcriptional regulation, and signaling pathways. Here, we show that TRIM15 co-localized to focal adhesions through homo-dimerization and significantly suppressed cell migration. Domain mapping analysis indicated that B-box2 and PRY domains were essential for TRIM15 localization to focal adhesions and inhibition of cell migration. Our protein-protein interaction screen of TRIM15 with the integrin adhesome identified several TRIM15 interacting proteins including coronin 1B, cortactin, filamin binding LIM protein1, and vasodilator-stimulated phosphoprotein, which are involved in actin cytoskeleton dynamics. TRIM15 expression was tissue-restricted and downregulated in colon cancer. Level of TRIM15 expression was associated with colon cancer cell migration, as well as both in vitro and in vivo tumor growth. These data provide novel insights into the role of TRIM15 as an additional component of the integrin adhesome, regulating cell migration, and suggest that TRIM15 may function as a tumor suppressor of colon cancer.
Insights
Tripartite motif containing 15 (TRIM15) protein suppresses cell migration by localizing to focal adhesions. TRIM15 downregulation in colon cancer correlates with increased cell migration and tumor growth, suggesting a tumor suppressor role.
Area of Science:
- Cell Biology
- Molecular Biology
- Cancer Research
Background:
- Tripartite motif containing (TRIM) proteins are involved in diverse biological processes.
- The specific functions of TRIM15 in cell regulation and cancer are not fully understood.
Purpose of the Study:
- To investigate the role of TRIM15 in cell migration and its potential involvement in colon cancer.
- To identify TRIM15 interacting proteins within the integrin adhesome.
Main Methods:
- Co-localization studies to determine TRIM15 localization.
- Domain mapping to identify critical functional regions.
- Protein-protein interaction screening with the integrin adhesome.
- Analysis of TRIM15 expression levels in colon cancer tissues.
Main Results:
- TRIM15 localizes to focal adhesions via homo-dimerization and suppresses cell migration.
- B-box2 and PRY domains are crucial for TRIM15's localization and inhibitory effects on migration.
- TRIM15 interacts with proteins involved in actin cytoskeleton dynamics.
- TRIM15 is downregulated in colon cancer, and its expression level correlates with migration and tumor growth.
Conclusions:
- TRIM15 acts as a regulator of cell migration by integrating into the integrin adhesome.
- TRIM15 functions as a tumor suppressor in colon cancer, with its downregulation promoting tumor progression.
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