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The Roles, Mechanisms, and Clinical Significance of Long Non-coding RNA MSC-AS1 in Cancer
Jingjie Yang1,2, Fan Peng1,2, Kexing Liu1,2
1Hubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges University, Yichang, 443002, China.
Abstract:
Musculin antisense RNA 1 (MSC-AS1) is a long non-coding RNA (lncRNA) located on human chromosome 8q13.3-q21.11. Emerging evidence shows that MSC-AS1 is either upregulated or downregulated in 16 types of human cancers, and is associated with clinical pathological features and patient prognosis in 12 of these cancers. It is widely believed that the dysregulation of MSCAS1 contributes to tumor cell growth, metastasis, epithelial-mesenchymal transition (EMT) progression, metabolic reprogramming, and drug resistance formation. Mechanistically, MSC-AS1 can act as a competing endogenous RNA (ceRNA) by sponging 14 miRNAs to affect the expression of downstream mRNAs, or it may directly interact with proteins, both of which contribute to the activation of the PI3K/AKT and Wnt/β-catenin signaling pathways. Our review study suggests that MSC-AS1 is a potential cancer biomarker and therapeutic target. In summary, we have explained the research on MSC-AS1 related to cancer treatment, its expression patterns, functional characteristics, and molecular mechanisms in malignant tumors. We have further emphasized its significance in clinical prognosis and therapeutic applications.
Insights
Musculin antisense RNA 1 (MSC-AS1), a long non-coding RNA, is dysregulated in numerous cancers. Its aberrant expression impacts tumor progression and patient outcomes, highlighting its potential as a cancer biomarker and therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Musculin antisense RNA 1 (MSC-AS1) is a long non-coding RNA (lncRNA) implicated in various human cancers.
- Its expression is altered in 16 cancer types, correlating with clinical features and prognosis in 12.
Purpose of the Study:
- To review the role of MSC-AS1 in cancer, including its expression patterns, functional roles, and molecular mechanisms.
- To evaluate MSC-AS1 as a potential cancer biomarker and therapeutic target.
Main Methods:
- Literature review of studies investigating MSC-AS1 in human cancers.
- Analysis of MSC-AS1 expression, functional impacts, and mechanistic pathways.
Main Results:
- MSC-AS1 dysregulation is linked to tumor growth, metastasis, epithelial-mesenchymal transition (EMT), metabolic reprogramming, and drug resistance.
- MSC-AS1 functions as a competing endogenous RNA (ceRNA) sponging miRNAs and directly interacts with proteins, activating PI3K/AKT and Wnt/β-catenin pathways.
Conclusions:
- MSC-AS1 plays a significant role in the development and progression of various cancers.
- MSC-AS1 holds promise as a diagnostic biomarker and a therapeutic target for cancer treatment.
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