Affiliation:
1. Department of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, 4301 W Markham St., Little Rock, AR 72205, USA
Abstract
Human Endogenous Retrovirus Sequences (HERVs) constitute up to 8% of the human genome, yet not all HERVs remain silent passengers within our genomes. Some HERVs, especially HERV type K (HERV-K), have been found to be frequently transactivated in a variety of inflammatory diseases and human cancers. Np9, a small protein translated from the HERV-K env reading frame, has been reported as an oncogenic protein and is present in a variety of tumors and transformed cells. The Np9 protein can crosstalk with many cellular factors and is involved in the pathogenicity of various diseases, including some oncogenic virus infections. In the current review, we summarize recent findings about Np9 clinical relevance/implications, its mediated cellular functions/mechanisms, and potential targeted therapies in development.
Funder
Arkansas Bioscience Institute
DoD Lung Cancer Research Program (LCRP) Concept Award
Reference33 articles.
1. “Reverse genomics” and human endogenous retroviruses;Markovitz;Trans. Am. Clin. Climatol. Assoc.,2014
2. Human Endogenous Retrovirus Type K (HERV-K) Particles Package and Transmit HERV-K-Related Sequences;Kaplan;J. Virol.,2015
3. Identification and characterization of novel human endogenous retrovirus families by phylogenetic screening of the human genome mapping project database;Tristem;J. Virol.,2000
4. Shin, W., Mun, S., and Han, K. (2023). Human Endogenous Retrovirus-K (HML-2)-Related Genetic Variation: Human Genome Diversity and Disease. Genes, 14.
5. Xue, B., Sechi, L.A., and Kelvin, D.J. (2020). Human Endogenous Retrovirus K (HML-2) in Health and Disease. Front. Microbiol., 11.
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