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Decoding the functional landscape of long non-coding RNAs in hepatocellular carcinoma: molecular mechanisms, clinical
Humera Naveed1, Zain-Ul Abidien1, Kaleem Maqsood1
1University of the Punjab, Lahore, Pakistan.
Abstract:
Hepatocellular carcinoma (HCC) remains the third leading cause of cancer-related mortality worldwide, with limited treatment efficacy and poor prognosis, particularly in advanced-stage disease. Despite progress in diagnostic imaging and systemic therapies, early detection and effective targeted interventions remain major clinical challenges. Long non-coding RNAs (lncRNAs), a class of regulatory RNA molecules exceeding 200 nucleotides in length, have emerged as essential regulators of oncogenic signaling, metabolism, and tumor microenvironment in HCC. This review provides a comprehensive overview of the molecular mechanisms, biological functions, and clinical relevance of key lncRNAs involved in HCC progression. We summarize the dual roles of lncRNAs as oncogenic drivers and tumor suppressors, with particular emphasis on oncogenic lncRNAs including CYTOR, UCA1, MALAT1, SPRY4-IT1, uc001ncr, AF085935, HULC, and HOTAIR. Their regulatory functions are discussed within major cancer-associated signaling networks, including the PI3K/AKT/mTOR, Wnt/β-catenin, TGF-β/NF-κB, and EMT-associated pathways. Furthermore, each lncRNA is discussed in the context of its expression pattern, endogenous RNA (ceRNA) interactions, molecular partners, and functional contributions to cellular proliferation, invasion, metastasis, angiogenesis, immune modulation, and therapeutic resistance. In addition, we explore the emerging potential of lncRNAs as minimally invasive diagnostic and prognostic biomarkers, owing to their stability and detectability in tissue and circulating biofluids. We also discuss recent advances in RNA- targeted therapeutic strategies, including RNA interference, siRNA-mediated silencing, antisense oligonucleotides, and CRISPR-based genome editing approaches. Collectively, this review highlights the importance of integrating lncRNA expression signatures into personalized HCC management and the promising role of lncRNA-based diagnostics and therapeutics in transforming the future landscape of liver cancer detection, prognosis, and treatment.
Insights
Long non-coding RNAs (lncRNAs) are key regulators in hepatocellular carcinoma (HCC), influencing its progression and treatment. This review explores lncRNAs
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Hepatocellular carcinoma (HCC) is a leading cause of cancer mortality with limited treatment options.
- Early detection and targeted therapies for HCC remain significant clinical challenges.
- Long non-coding RNAs (lncRNAs) are emerging as critical regulators in HCC development and progression.
Purpose of the Study:
- To provide a comprehensive overview of lncRNAs in HCC.
- To elucidate the molecular mechanisms and biological functions of key lncRNAs in HCC progression.
- To discuss the clinical relevance, diagnostic potential, and therapeutic applications of lncRNAs in HCC.
Main Methods:
- Literature review of lncRNAs in hepatocellular carcinoma.
- Analysis of lncRNA molecular mechanisms, signaling pathways, and functional roles.
- Exploration of lncRNA-based diagnostics and therapeutic strategies.
Main Results:
- lncRNAs exhibit dual roles as oncogenic drivers and tumor suppressors in HCC.
- Key oncogenic lncRNAs (e.g., CYTOR, UCA1, MALAT1) regulate major cancer pathways (PI3K/AKT/mTOR, Wnt/β-catenin, TGF-β/NF-κB, EMT).
- lncRNAs show potential as diagnostic/prognostic biomarkers and therapeutic targets in HCC.
Conclusions:
- lncRNAs are crucial in HCC pathogenesis, offering insights into molecular mechanisms.
- lncRNA expression signatures can personalize HCC management.
- lncRNA-based diagnostics and therapeutics hold promise for improving HCC outcomes.
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