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Function and Mechanism of Small Nucleolar RNAs (snoRNAs) and Their Host Genes (SNHGs) in Malignant Tumors
Jiaji Yu1, Yingjie Shao1,2, Wendong Gu1,2
1Department of Radiation Oncology, Changzhou Medical Center, Nanjing Medical University, 185 Juqian Street, Changzhou 213003, China.
Abstract:
Small nucleolar RNAs (snoRNAs) and their host genes (SNHGs) are non-coding RNAs that are integral to tumorigenesis and progression. snoRNAs contribute to tumor progression primarily through RNA modification and engagement in intracellular signaling, and by serving as precursors for small nucleolar RNA-derived RNAs (sdRNAs) that exert microRNA (miRNA)-like or epigenetic regulatory functions. SNHGs modulate key tumor cell behaviors-including proliferation, metastasis, and resistance to therapy-through competing endogenous RNA (ceRNA)-mediated interactions and epigenetic mechanisms. Their combined influence significantly impacts patient prognosis. Across diverse malignancies such as neurologic, bone, and head and neck cancers, snoRNAs and SNHGs exhibit cancer-specific regulatory dynamics; for instance, in glioblastoma, snoRNAs and their derived fragments (sdRNAs) contribute to intratumoral heterogeneity by mediating both metabolic reprogramming and epigenetic remodeling, while their mediated modulation of cellular proliferation and metastatic potential is evident in breast cancer. Concurrently, several snoRNAs and SNHGs have emerged as potential diagnostic and prognostic biomarkers, as well as therapeutic targets. Preclinical interventions targeting select snoRNAs or SNHGs have demonstrated promising therapeutic outcomes. This study reviews current insights into the oncogenic functions and signaling networks associated with dysregulated snoRNAs and SNHGs in malignancies, while highlighting novel avenues for future investigation in this domain.
Insights
Small nucleolar RNAs (snoRNAs) and their host genes (SNHGs) are key players in cancer development. Dysregulation of these non-coding RNAs impacts tumor progression, patient prognosis, and offers potential diagnostic and therapeutic targets.
Area of Science:
- Oncology
- Molecular Biology
- Non-coding RNA Research
Background:
- Small nucleolar RNAs (snoRNAs) and their host genes (SNHGs) are non-coding RNAs implicated in tumorigenesis.
- Dysregulated snoRNAs and SNHGs influence tumor progression via RNA modification, intracellular signaling, and epigenetic mechanisms.
- These molecules impact critical cancer cell behaviors like proliferation, metastasis, and therapy resistance.
Purpose of the Study:
- To review the oncogenic functions and signaling networks of dysregulated snoRNAs and SNHGs in malignancies.
- To highlight their roles in diverse cancers, including glioblastoma and breast cancer.
- To explore their potential as diagnostic/prognostic biomarkers and therapeutic targets.
Main Methods:
- Literature review of current research on snoRNAs and SNHGs in cancer.
- Analysis of their involvement in tumorigenesis, progression, and patient prognosis.
- Examination of preclinical intervention strategies targeting these non-coding RNAs.
Main Results:
- snoRNAs and SNHGs significantly impact tumor progression and patient outcomes across various cancers.
- They contribute to intratumoral heterogeneity, metabolic reprogramming, and epigenetic remodeling.
- Several snoRNAs and SNHGs show promise as biomarkers and therapeutic targets, with preclinical interventions yielding positive results.
Conclusions:
- Dysregulated snoRNAs and SNHGs are crucial in cancer development and progression, affecting multiple cellular processes.
- Their specific roles vary across cancer types, influencing heterogeneity and therapeutic resistance.
- Targeting snoRNAs and SNHGs represents a promising avenue for novel cancer diagnostics and therapeutics.
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