Literature DB >> 33478113

Cancer, Retrogenes, and Evolution.

Klaudia Staszak1, Izabela Makałowska1.   

Abstract

This review summarizes the knowledge about retrogenes in the context of cancer and evolution. The retroposition, in which the processed mRNA from parental genes undergoes reverse transcription and the resulting cDNA is integrated back into the genome, results in additional copies of existing genes. Despite the initial misconception, retroposition-derived copies can become functional, and due to their role in the molecular evolution of genomes, they have been named the "seeds of evolution". It is convincing that retrogenes, as important elements involved in the evolution of species, also take part in the evolution of neoplastic tumors at the cell and species levels. The occurrence of specific "resistance mechanisms" to neoplastic transformation in some species has been noted. This phenomenon has been related to additional gene copies, including retrogenes. In addition, the role of retrogenes in the evolution of tumors has been described. Retrogene expression correlates with the occurrence of specific cancer subtypes, their stages, and their response to therapy. Phylogenetic insights into retrogenes show that most cancer-related retrocopies arose in the lineage of primates, and the number of identified cancer-related retrogenes demonstrates that these duplicates are quite important players in human carcinogenesis.

Entities:  

Keywords:  cancer; retrogenes; retroposition; species evolution; tumor evolution

Year:  2021        PMID: 33478113      PMCID: PMC7835786          DOI: 10.3390/life11010072

Source DB:  PubMed          Journal:  Life (Basel)        ISSN: 2075-1729


  96 in total

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5.  Inter-population Differences in Retrogene Loss and Expression in Humans.

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9.  The Pan-Cancer analysis of pseudogene expression reveals biologically and clinically relevant tumour subtypes.

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Review 10.  Role of Pseudogenes in Tumorigenesis.

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Journal:  Cancers (Basel)       Date:  2018-08-01       Impact factor: 6.639

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Journal:  Cells       Date:  2021-04-15       Impact factor: 6.600

2.  SARS-CoV-2-Host Chimeric RNA-Sequencing Reads Do Not Necessarily Arise From Virus Integration Into the Host DNA.

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  2 in total

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