Abstract

Recently, Up-frameshift protein 1 (UPF1) is reported to be downregulated in various cancers and its low expression is closely correlated with poor prognosis. UPF1 is well known as a master regulator of nonsense-mediated mRNA decay (NMD), which serves as a highly conserved mRNA surveillance process protecting cells from aberrant toxic transcripts. Due to dysfunction of UPF1, NMD fails to proceed, which contributes to tumor initiation and progression. This review shows a brief summary of the aberrant expression, functional roles and molecular mechanisms of UPF1 during tumorigenesis. Increasing evidence has indicated that UPF1 could serve as a potential biomarker for cancer diagnosis and treatment for future clinical applications in cancer.

Highlights

  • We summarize recent studies on the role of Up-frameshift protein 1 (UPF1) in cancers, including those focused on its aberrant expression, biological functions, and associated clinical features, in addition to its regulatory network, and further debate the prognostic and therapeutic values of UPF1 in human cancers

  • Cao et al [33] reported that UPF1 level was downregulated in 160 lung adenocarcinoma (LADC) tissues compared with matched adjacent normal tissues, a recent study uncovered by Han and colleagues focused on the biological role of UPF1 in LADC, and confirmed an inconsistently obvious upregulation of UPF1 in LADC cells [34]

  • Several researches showed that UPF1 was significantly downregulated and acted as a tumor suppressor in most types of cancer including hepatocellular cancer (HCC), gastric cancer (GC), thyroid cancer (TC), ovarian cancer (OC) and glioma

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Summary

Expression of UPF1 in cancer

Several researches have reported that UPF1 act as tumor suppressor and was downregulated in various cancers. UPF1 downregulation has been consistently revealed in a great diversity of other tumor types, including hepatocellular cancer (HCC) [23, 25,26,27], gastric cancer (GC) [32], inflammatory myofibroblastic tumors (IMT) [36], thyroid cancer (TC) [37], ovarian cancer (OC) [38] and glioma [39]. These studies demonstrated that UPF1 has a tumor-suppressive role. Maybe the contributors to dysregulated expression of UPF1 in cancers are various, including tumor cell, pathological type and so on, which still need further investigations

Epigenetic alterations
Genomic alteration
Aberrant splicing of UPF1 in cancers
Function of UPF1 in cancer
The involvement of UPF1 in EMT
Mechanistic model of UPF1
UPF1 as a prognostic marker
Potential therapeutic target
10. Concluding remarks and future perspectives
14. Funding
Findings
16. References
Full Text
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