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Review
. 2020 Aug 12;12(8):2260.
doi: 10.3390/cancers12082260.

Anti-cancer Immunotherapies Targeting Telomerase

Affiliations
Review

Anti-cancer Immunotherapies Targeting Telomerase

Simone Negrini et al. Cancers (Basel). .

Abstract

Telomerase is a reverse transcriptase that maintains telomeres length, compensating for the attrition of chromosomal ends that occurs during each replication cycle. Telomerase is expressed in germ cells and stem cells, whereas it is virtually undetectable in adult somatic cells. On the other hand, telomerase is broadly expressed in the majority of human tumors playing a crucial role in the replicative behavior and immortality of cancer cells. Several studies have demonstrated that telomerase-derived peptides are able to bind to HLA (human leukocyte antigen) class I and class II molecules and effectively activate both CD8+ and CD4+ T cells subsets. Due to its broad and selective expression in cancer cells and its significant immunogenicity, telomerase is considered an ideal universal tumor-associated antigen, and consequently, a very attractive target for anti-cancer immunotherapy. To date, different telomerase targeting immunotherapies have been studied in pre-clinical and clinical settings, these approaches include peptide vaccination and cell-based vaccination. The objective of this review paper is to discuss the role of human telomerase in cancer immunotherapy analyzing recent developments and future perspectives in this field.

Keywords: cancer; clinical trials; hTERT; immunotherapy; telomerase; vaccine.

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Conflict of interest statement

The authors declare no conflict of interest.

References

    1. De Lange T. How telomeres solve the end-protection problem. Science. 2009;326:948–952. doi: 10.1126/science.1170633. - DOI - PMC - PubMed
    1. Pfeiffer V., Lingner J. Replication of telomeres and the regulation of telomerase. Cold Spring Harb. Perspect. Biol. 2013;5:a010405. doi: 10.1101/cshperspect.a010405. - DOI - PMC - PubMed
    1. Roake C.M., Artandi S.E. Regulation of human telomerase in homeostasis and disease. Nat. Rev. Mol. Cell Biol. 2020;21:384–397. doi: 10.1038/s41580-020-0234-z. - DOI - PMC - PubMed
    1. Kim N.W., Piatyszek M.A., Prowse K.R., Harley C.B., West M.D., Ho P.L., Coviello G.M., Wright W.E., Weinrich S.L., Shay J.W. Specific association of human telomerase activity with immortal cells and cancer. Science. 1994;266:2011–2015. doi: 10.1126/science.7605428. - DOI - PubMed
    1. Dogan F., Biray Avci C. Correlation between telomerase and mTOR pathway in cancer stem cells. Gene. 2018;641:235–239. doi: 10.1016/j.gene.2017.09.072. - DOI - PubMed