Unraveling the ncRNA landscape that governs colorectal cancer: A roadmap to personalized therapeutics

Prof. Hamdy, Nadia M.; Zaki, Mohamed Bakr; Rizk, Nehal I; Abdelmaksoud, Nourhan M; Abd-Elmawla, Mai A; Ismail, Rehab A; Abulsoud, Ahmed I;

Abstract


Colorectal cancer (CRC) being one of the most common malignancies, has a significant death rate, especially when detected at an advanced stage. In most cases, the fundamental aetiology of CRC remains unclear despite the identification of several environmental and intrinsic risk factors. Numerous investigations, particularly in the last ten years, have indicated the involvement of epigenetic variables in this type of cancer. The development, progression, and metastasis of CRC are influenced by long non-coding RNAs (lncRNAs), which are significant players in the epigenetic pathways. LncRNAs are implicated in diverse pathological processes in CRC, such as liver metastasis, epithelial to mesenchymal transition (EMT), inflammation, and chemo-/radioresistance. It has recently been determined that CRC cells and tissues exhibit dysregulation of tens of oncogenic and tumor suppressor lncRNAs. Serum samples from CRC patients exhibit dysregulated expressions of several of these transcripts, offering a non-invasive method of detecting this kind of cancer. In this review, we outlined the typical paradigms of the deregulated lncRNA which exert significant role in the underlying molecular mechanisms of CRC initiation and progression. We comprehensively discuss the role of lncRNAs as innovative targets for CRC prognosis and treatment.


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Title Unraveling the ncRNA landscape that governs colorectal cancer: A roadmap to personalized therapeutics
Authors Prof. Hamdy, Nadia M. ; Zaki, Mohamed Bakr; Rizk, Nehal I; Abdelmaksoud, Nourhan M; Abd-Elmawla, Mai A; Ismail, Rehab A; Abulsoud, Ahmed I
Keywords Colorectal Cancer (CRC); In silico; LncRNA; Non-invasive biomarkers; Precision medicine; Signaling pathways; ncRNA
Issue Date 1-Oct-2024
Journal Life sciences 
ISSN 00243205
DOI 10.1016/j.lfs.2024.122946
PubMed ID 39122108
Scopus ID 2-s2.0-85200637002

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