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Updated: May 25, 2025

Detection of Modified Forms of Cytosine Using Sensitive Immunohistochemistry
Published on: August 16, 2016
Detection, molecular function and mechanisms of m5C in cancer
Linhui Zhang1,2,3, Yuelong Li1, Liqing Li1,2,3
1Department of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Abstract:
Interest in RNA posttranscriptional modifications, particularly 5-methylcytosine (m5C), has surged in recent years. Studies have shown that m5C plays a key role in cellular processes and is closely linked to tumourigenesis. This growing focus emphasises the importance of understanding the diverse impacts of m5C modifications in both normal cellular functions and cancer development. Moreover, strides in methodologies for discerning m5C have facilitated intricate transcriptome cartography of RNA methylation at the solitary nucleotide echelon. This technical progress has fueled a surge in m5C-centric investigations, facilitating further exploration of this RNA modification. This review provides a comprehensive analysis of the oncogenic potential of m5C RNA modification, elucidating the precise molecular mechanisms driving its role in cancer development. It consolidates current knowledge regarding the biological consequences of m5C RNA modification in tumour cells. Understanding the role of methylation-related processes in tumourigenesis shows promise for advancing cancer diagnosis and therapeutic strategies. HIGHLIGHTS: m5C modifications are dynamically regulated by writers, readers, and erasers, influencing cancer progression, metastasis, and immune evasion. Distinct m5C regulatory networks exist across cancers, modulating oncogenic pathways and therapy responses. m5C signatures serve as biomarkers for cancer prognosis and treatment stratification, highlighting their role in precision oncology.
Insights
5-methylcytosine (m5C) RNA modifications are crucial in cancer development, influencing progression and immune evasion. Understanding m5C regulatory networks offers new avenues for cancer biomarkers and precision oncology treatments.
Area of Science:
- Molecular Biology
- Oncology
- Epigenetics
Background:
- Recent surge in interest in RNA posttranscriptional modifications, specifically 5-methylcytosine (m5C).
- m5C is implicated in fundamental cellular processes and closely associated with tumorigenesis.
- Advancements in m5C detection methodologies enable single-nucleotide resolution transcriptome mapping.
Purpose of the Study:
- To comprehensively review the oncogenic potential of m5C RNA modifications.
- To elucidate the molecular mechanisms underlying m5C's role in cancer development.
- To consolidate current knowledge on the biological impact of m5C in tumor cells.
Main Methods:
- Literature review and synthesis of existing research on m5C RNA modifications.
- Analysis of molecular mechanisms linking m5C to cancer.
- Consolidation of data on m5C's biological consequences in tumor cells.
Main Results:
- m5C modifications are dynamically regulated by "writers," "readers," and "erasers," affecting cancer progression, metastasis, and immune evasion.
- Specific m5C regulatory networks are observed across different cancers, influencing oncogenic pathways and treatment responses.
- m5C signatures are emerging as valuable biomarkers for cancer prognosis and treatment stratification.
Conclusions:
- Understanding m5C's role in tumorigenesis holds promise for improved cancer diagnosis and therapeutics.
- m5C regulatory networks are critical determinants of cancer phenotypes and therapeutic vulnerabilities.
- m5C-based biomarkers are key to advancing precision oncology.
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