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Updated: Jul 3, 2026

Multiomics Analysis of TMEM200A as a Pan-Cancer Biomarker
Published on: September 15, 2023
Identification of potential genes/proteins regulated by Tiam1 in colorectal cancer by microarray analysis and
Li Liu1, Shuang Wang, Qingling Zhang
1Department of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, Guangdong Province, China.
Abstract:
Tiam1 (T-cell lymphoma invasion and metastasis-inducing protein 1), a guanine nucleotide exchange factor that activates Rac, is a colorectal cancer metastasis-related gene. In this study, we aimed to better understand the mechanism underlying Tiam1-mediated metastasis. We applied gene microarray and proteome analysis and compared expression of genes and proteins in a stable Tiam1-silencing colorectal cancer cell line and in a control cell line. Our analysis identified three genes, high-mobility group box1 (HMGB1), annexin IV (ANXA4) and phosphoglycerate mutase 1 (PGAM1) that were associated with Tiam1. Analysis of these proteins, which may be directly or indirectly regulated by Tiam1, may provide insight into the role and mechanism of Tiam1 in colorectal cancer metastasis.
Insights
T-cell lymphoma invasion and metastasis-inducing protein 1 (Tiam1) drives colorectal cancer metastasis. This study identified HMGB1, ANXA4, and PGAM1 as key associated genes, offering insights into Tiam1
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- T-cell lymphoma invasion and metastasis-inducing protein 1 (Tiam1) is a guanine nucleotide exchange factor implicated in colorectal cancer (CRC) metastasis.
- Understanding the molecular mechanisms of Tiam1-mediated metastasis is crucial for developing targeted therapies.
Purpose of the Study:
- To elucidate the underlying mechanisms of Tiam1-mediated metastasis in colorectal cancer.
- To identify novel genes and proteins regulated by Tiam1 in CRC.
Main Methods:
- Gene microarray and proteome analysis were employed.
- Comparison of gene and protein expression between a stable Tiam1-silencing CRC cell line and a control cell line.
Main Results:
- Three genes—high-mobility group box 1 (HMGB1), annexin IV (ANXA4), and phosphoglycerate mutase 1 (PGAM1)—were identified as associated with Tiam1.
- These genes/proteins may be directly or indirectly regulated by Tiam1.
Conclusions:
- HMGB1, ANXA4, and PGAM1 are potential key players in Tiam1-driven colorectal cancer metastasis.
- Further analysis of these associated proteins could reveal critical insights into Tiam1's role and mechanism in CRC progression.

