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Silencing MARCH2 Inhibits the Invasion, Migration, and EMT Transformation of Human Colorectal Cancer SW480 Cells
Yun Liu1, Ran Longyan2, Qingxi Guo1
1Department of Pathology, 556508Affiliated Hospital of Southwest Medical University, Luzhou, China.
Abstract:
Aim: This study aimed to investigate the role of MARCH2 (membrane-associated RING-CH2) in the progression, invasion, and migration of colorectal cancer (CRC). Methods: In this study, the expression levels of MARCH2 and E-cadherin in CRC tissues were detected by immunohistochemistry through retrospective study, and their correlation was analyzed. After silencing the MARCH2 gene using SiRNA MARCH2-1/-2, the invasion and migration abilities of SW480 cells were detected using Transwell and Scratch assay, respectively. Quantitative real-time PCR (qRT-PCR) and Western blotting assays were performed to detect the expression levels of epithelial-mesenchymal transition (EMT) related markers. Results: As compared to adjacent tissues, the MARCH2 expression level was significantly overexpressed in the CRC tissues, and correlated with tumor size, pathological grade, lymph node metastasis, and survival time. MARCH2 was negatively correlated with E-cadherin. MARCH2 silencing significantly restrained the invasion and migration abilities of SW480 cells in vitro. Meanwhile, the MARCH2 silencing also upregulated the mRNA and protein expression levels of E-cadherin and downregulated those of Vimentin. Conclusions: The high expression of MARCH2 was unfavorable for patients' survival. Thus, MARCH2 might be an independent predictor for CRC patients, affecting the invasion and metastasis of CRC through EMT.
Insights
High expression of membrane-associated RING-CH2 (MARCH2) is linked to colorectal cancer (CRC) progression and poor survival. Silencing MARCH2 inhibits CRC cell invasion and metastasis, suggesting MARCH2 is a potential biomarker for CRC.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Colorectal cancer (CRC) is a major global health concern.
- Understanding the molecular mechanisms driving CRC progression, invasion, and metastasis is crucial for developing effective treatments.
- The role of membrane-associated RING-CH2 (MARCH2) in CRC remains to be fully elucidated.
Purpose of the Study:
- To investigate the role of MARCH2 in the progression, invasion, and migration of colorectal cancer (CRC).
- To determine the correlation between MARCH2 expression and clinicopathological features and survival in CRC patients.
- To explore the underlying molecular mechanisms involving epithelial-mesenchymal transition (EMT).
Main Methods:
- Retrospective analysis of MARCH2 and E-cadherin expression in CRC tissues using immunohistochemistry.
- In vitro experiments involving MARCH2 gene silencing in SW480 CRC cells using siRNA.
- Assessment of cell invasion and migration using Transwell and Scratch assays.
- Quantitative real-time PCR (qRT-PCR) and Western blotting to analyze EMT markers.
Main Results:
- MARCH2 was significantly overexpressed in CRC tissues compared to adjacent tissues.
- High MARCH2 expression correlated with larger tumor size, advanced pathological grade, lymph node metastasis, and shorter survival time.
- MARCH2 silencing reduced CRC cell invasion and migration, upregulated E-cadherin, and downregulated Vimentin, indicating inhibition of EMT.
Conclusions:
- Elevated MARCH2 expression is associated with unfavorable prognosis in CRC patients.
- MARCH2 may serve as an independent prognostic biomarker for CRC.
- MARCH2 promotes CRC invasion and metastasis, potentially through the regulation of EMT.
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