VEVERKA, Pavel, Tomáš JANOVIČ and Ctirad HOFR. Quantitative Biology of Human Shelterin and Telomerase: Searching for the Weakest Point. International Journal of Molecular Sciences. Basel: Multidisciplinary Digital Publishing Institute, 2019, vol. 20, No 13, p. 1-13. ISSN 1422-0067. Available from: https://dx.doi.org/10.3390/ijms20133186.
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Basic information
Original name Quantitative Biology of Human Shelterin and Telomerase: Searching for the Weakest Point
Authors VEVERKA, Pavel (203 Czech Republic, belonging to the institution), Tomáš JANOVIČ (203 Czech Republic, belonging to the institution) and Ctirad HOFR (203 Czech Republic, guarantor, belonging to the institution).
Edition International Journal of Molecular Sciences, Basel, Multidisciplinary Digital Publishing Institute, 2019, 1422-0067.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10610 Biophysics
Country of publisher Switzerland
Confidentiality degree is not subject to a state or trade secret
WWW Full Text
Impact factor Impact factor: 4.556
RIV identification code RIV/00216224:14310/19:00107498
Organization unit Faculty of Science
Doi http://dx.doi.org/10.3390/ijms20133186
UT WoS 000477041100074
Keywords in English telomerase; shelterin; telomere; quantitative biology; protein-protein interaction; protein-DNA interaction; assembly; inhibitor; anticancer
Tags CF BIC, CF CELLIM, CF PROT, rivok
Tags Reviewed
Changed by Changed by: Mgr. Pavla Foltynová, Ph.D., učo 106624. Changed: 8/3/2020 19:41.
Abstract
The repetitive telomeric DNA at chromosome ends is protected from unwanted repair by telomere-associated proteins, which form the shelterin complex in mammals. Recent works have provided new insights into the mechanisms of how human shelterin assembles and recruits telomerase to telomeres. Inhibition of telomerase activity and telomerase recruitment to chromosome ends is a promising target for anticancer therapy. Here, we summarize results of quantitative assessments and newly emerged structural information along with the status of the most promising approaches to telomerase inhibition in cancer cells. We focus on the mechanism of shelterin assembly and the mechanisms of how shelterin affects telomerase recruitment to telomeres, addressing the conceptual dilemma of how shelterin allows telomerase action and regulates other essential processes. We evaluate how the identified critical interactions of telomerase and shelterin might be elucidated in future research of new anticancer strategies.
Links
GA16-20255S, research and development projectName: Molekulární mechanismus inhibice telomerázy: cílené zastavení dělení nádorových buněk
Investor: Czech Science Foundation
GA19-18226S, research and development projectName: Kritické interakce neuronového transkripčního faktoru REST se stabilizátorem TRF2: biofyzikální implikace pro návrh léčiv glioblastomu
Investor: Czech Science Foundation
LM2015043, research and development projectName: Česká infrastruktura pro integrativní strukturní biologii (Acronym: CIISB)
Investor: Ministry of Education, Youth and Sports of the CR
LM2015062, research and development projectName: Národní infrastruktura pro biologické a medicínské zobrazování
Investor: Ministry of Education, Youth and Sports of the CR
LQ1601, research and development projectName: CEITEC 2020 (Acronym: CEITEC2020)
Investor: Ministry of Education, Youth and Sports of the CR
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