# TM7SF2 as a Potential Biomarker in Colorectal Cancer: Implications for Metastasis

**Authors:** Inpyo Hong, Sooyoun Kim, Minho Lee, Seoin Han, Hak Chun Kim, Chong Woo Chu, Seong Geun Kim, Min Kyung Kim, Chang Jin Kim, Dong Hyun Kang, Tae Sung Ahn, Moo Jun Baek, Mudasir Hussain, Hyog Young Kwon, Dongjun Jeong

PMC · DOI: 10.3390/curroncol32020114 · 2025-02-17

## TL;DR

This study identifies TM7SF2 as a potential biomarker for predicting metastasis in colorectal cancer, which could help improve survival rates through early detection.

## Contribution

The study validates TM7SF2 as a novel biomarker for metastasis prediction in colorectal cancer through experimental and clinical analysis.

## Key findings

- TM7SF2 expression is associated with clinical stage and reduced survival rates in CRC patients.
- TM7SF2 knockdown suppresses cell proliferation, migration, invasion, and colony formation in CRC cell lines.

## Abstract

Colorectal cancer (CRC) is a commonly fatal cancer and ranks as the fourth most prevalent in men and third in women worldwide. While early-stage survival rates are high, they significantly decrease with recurrence and metastasis. Thus, the early detection and treatment of metastasis-related factors can significantly improve survival rates. In this study, the transmembrane 7 superfamily member 2 (TM7SF2) gene was validated as a biomarker for predicting metastasis in CRC. Immunohistochemical staining was performed on 236 CRC tissues, and the clinicopathological factors of patients with CRC were analyzed. This evaluation revealed that TM7SF2 expression is associated with the clinical stage. Kaplan–Meier analysis confirmed the relationship between the survival rate of CRC patients and TM7SF2 expression, showing a decrease in survival rate with TM7SF2 overexpression (log-rank, p < 0.001). TM7SF2 expression was also confirmed in two pairs of primary and metastatic cell lines (SW480 and SW620). TM7SF2 knockdown was executed using siRNAs in SW480 and SW620 cells, which exhibit high expression levels. The knockdown was verified using RT-PCR and immunoblotting. Functional studies investigated the effects of TM7SF2 on cell proliferation, migration, invasion, and colony formation, revealing that all these functions were suppressed in the CRC cell lines following TM7SF2 knockdown. Therefore, TM7SF2 shows promise as a biomarker for the prevention of colorectal cancer.

## Linked entities

- **Genes:** TM7SF2 (transmembrane 7 superfamily member 2) [NCBI Gene 7108]
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** TM7SF2 (transmembrane 7 superfamily member 2) [NCBI Gene 7108] {aka ANG1, C14SR, DHCR14A, NET47}
- **Diseases:** Metastasis (MESH:D009362), cancer (MESH:D009369), CRC (MESH:D015179)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** SW620 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0547), SW480 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0546)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11854686/full.md

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Source: https://tomesphere.com/paper/PMC11854686