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Updated: Jan 24, 2026

A Robust Discovery Platform for the Identification of Novel Mediators of Melanoma Metastasis
Published on: March 8, 2022
Long noncoding RNA CPS1-IT1 suppresses melanoma cell metastasis through inhibiting Cyr61 via competitively binding to
Xiaobo Zhou1, Yamin Rao2, Qilin Sun3
1Department of Plastic and Reconstructive Surgery, Shanghai Ninth People's Hospital, Affiliated to Shanghai Jiaotong University School of Medicine, Center for Specialty Strategy Research of Shanghai JiaoTong University China Hospital Development Institute, Shanghai, China.
Abstract:
Long noncoding RNA CPS1-IT1 is recently recognized as a tumor suppressor in several cancers. Here, we investigate the role of CPS1-IT1 in human melanoma. Presently, our study reveals the low expression of CPS1-IT1 in human melanoma tissues and cell lines, which is significantly associated with metastasis and tumor stage. Besides, the potential of CPS1-IT1 as a prognosis-predictor is strongly indicated. Functionally, CPS1-IT1 overexpression inhibits cell migration, invasion, epithelial-mesenchymal transition, and angiogenesis in melanoma cells. CYR61, an angiogenic factor that participates in tumor metastasis as well as a recognized oncogene in melanoma, is shown to be confined under CPS1-IT1 overexpression in melanoma cells. Furthermore, enforced expression of Cyr61 in CPS1-IT1-silenced melanoma cells dramatically normalized the protein level of Cyr61 and that of its downstream targets vascular endothelial growth factor and matrix metalloproteinase-9, as well as the repressive effect of CPS1-IT1 overexpression on melanoma cell metastasis. BRG1, a core component of SWI/SNF complex, is implied to interact with both CPS1-IT1 and Cyr61 in melanoma cells. Moreover, CPS1-IT1 negatively regulates Cyr61 expression by blocking the binding of BRG1 to Cyr61 promoter. Jointly, CPS1-IT1 controls melanoma metastasis through impairing Cyr61 expression via competitively binding with BRG1, uncovering a novel potential therapeutic and prognostic biomarker for patients with melanoma.
Insights
Long noncoding RNA CPS1-IT1 acts as a tumor suppressor in melanoma. Its reduced expression correlates with metastasis and poor prognosis, suggesting it
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long noncoding RNAs (lncRNAs) are increasingly recognized for their roles in cancer.
- CPS1-IT1 has emerged as a potential tumor suppressor in various cancers.
- The specific function of CPS1-IT1 in human melanoma remains largely unexplored.
Purpose of the Study:
- To investigate the role of CPS1-IT1 in human melanoma.
- To determine the association of CPS1-IT1 expression with clinical features and prognosis.
- To elucidate the molecular mechanisms underlying CPS1-IT1's function in melanoma metastasis.
Main Methods:
- Quantitative real-time PCR to assess CPS1-IT1 expression levels.
- Analysis of the correlation between CPS1-IT1 expression and clinicopathological parameters.
- Cellular assays including migration, invasion, and angiogenesis assays.
- Western blotting to evaluate protein expression levels.
- Chromatin immunoprecipitation assays to investigate protein-DNA interactions.
Main Results:
- CPS1-IT1 expression is significantly downregulated in human melanoma tissues and cell lines.
- Low CPS1-IT1 expression is associated with advanced tumor stage and metastasis.
- CPS1-IT1 overexpression inhibits melanoma cell migration, invasion, epithelial-mesenchymal transition, and angiogenesis.
- CPS1-IT1 suppresses melanoma metastasis by inhibiting the oncogene CYR61 expression via interaction with BRG1.
- CPS1-IT1 acts as a potential prognostic biomarker for melanoma.
Conclusions:
- CPS1-IT1 functions as a tumor suppressor in human melanoma.
- CPS1-IT1 negatively regulates melanoma cell metastasis by targeting the CYR61/BRG1 axis.
- CPS1-IT1 holds promise as a novel therapeutic target and prognostic biomarker for melanoma patients.
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