PVT1 lncRNA in lung cancer: A key player in tumorigenesis and therapeutic opportunities

The lncRNA PVT1 has emerged as a pivotal component in the intricate landscape of cancer pathogenesis, particularly in lung cancer. PVT1, situated in the 8q24 chromosomal region, has garnered attention for its aberrant expression patterns in lung cancer, correlating with tumor progression, metastasis...

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Veröffentlicht in:Pathology, research and practice research and practice, 2024-01, Vol.253, p.155019-155019, Article 155019
Hauptverfasser: Hakami, Mohammed Ageeli, Hazazi, Ali, Khan, Farhan R., Abdulaziz, Osama, Alshaghdali, Khalid, Abalkhail, Adil, Nassar, Somia A., Omar, Bashir Ibrahim A., Almarshadi, Fahad, Gupta, Gaurav, Binshaya, Abdulkarim S.
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Sprache:eng
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Zusammenfassung:The lncRNA PVT1 has emerged as a pivotal component in the intricate landscape of cancer pathogenesis, particularly in lung cancer. PVT1, situated in the 8q24 chromosomal region, has garnered attention for its aberrant expression patterns in lung cancer, correlating with tumor progression, metastasis, and poor prognosis. Numerous studies have unveiled the diverse mechanisms PVT1 contributes to lung cancer pathogenesis. It modulates critical pathways, such as cell proliferation, apoptosis evasion, angiogenesis, and epithelial-mesenchymal transition. PVT1's interactions with other molecules, including microRNAs and proteins, amplify its oncogenic influence. Recent advancements in genomic and epigenetic analyses have also illuminated the intricate regulatory networks that govern PVT1 expression. Understanding PVT1's complex involvement in lung cancer holds substantial clinical implications. Targeting PVT1 presents a promising avenue for developing novel diagnostic biomarkers and therapeutic interventions. This abstract encapsulates the expanding knowledge regarding the oncogenic role of PVT1 in lung cancer, underscoring the significance of further research to unravel its complete mechanistic landscape and exploit its potential for improved patient outcomes. [Display omitted]
ISSN:0344-0338
1618-0631
DOI:10.1016/j.prp.2023.155019