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TM7SF2 as a Potential Biomarker in Colorectal Cancer: Implications for Metastasis
Inpyo Hong1, Sooyoun Kim1, Minho Lee1
1Department of Pathology, College of Medicine, Soonchunhyang University, Dongnam-gu, Cheonan 31151, Republic of Korea.
Current Oncology (Toronto, Ont.)
|February 25, 2025
Summary
Transmembrane 7 superfamily member 2 (TM7SF2) acts as a biomarker for colorectal cancer (CRC) metastasis. Lowering TM7SF2 expression in CRC cells reduces proliferation, migration, and invasion, suggesting its potential for cancer prevention.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Biomarkers
Background:
- Colorectal cancer (CRC) is a leading cause of cancer death globally.
- Metastasis significantly reduces survival rates in CRC patients.
- Early detection of metastasis-related factors is crucial for improving patient outcomes.
Purpose of the Study:
- To validate the transmembrane 7 superfamily member 2 (TM7SF2) gene as a biomarker for predicting CRC metastasis.
- To investigate the functional role of TM7SF2 in CRC cell behavior.
Main Methods:
- Immunohistochemical staining of 236 CRC tissues to analyze TM7SF2 expression.
- Kaplan-Meier survival analysis correlating TM7SF2 expression with patient survival.
- TM7SF2 knockdown using siRNAs in CRC cell lines (SW480, SW620) followed by RT-PCR and immunoblotting.
- Functional assays assessing cell proliferation, migration, invasion, and colony formation.
Main Results:
- TM7SF2 expression was significantly associated with the clinical stage of CRC.
- Overexpression of TM7SF2 correlated with decreased survival rates in CRC patients (log-rank, p < 0.001).
- TM7SF2 knockdown suppressed cell proliferation, migration, invasion, and colony formation in CRC cell lines.
Conclusions:
- TM7SF2 is a promising biomarker for predicting metastasis in colorectal cancer.
- TM7SF2 plays a significant role in promoting CRC cell proliferation and metastasis.
- Targeting TM7SF2 may offer a novel therapeutic strategy for colorectal cancer prevention.

