Zobrazeno 1 - 10
of 82
pro vyhledávání: '"G-Quadruplexe"'
Autor:
Shalu Sharma, Ananda Kishore Mukherjee, Shuvra Shekhar Roy, Sulochana Bagri, Silje Lier, Meenakshi Verma, Antara Sengupta, Manish Kumar, Gaute Nesse, Deo Prakash Pandey, Shantanu Chowdhury
Publikováno v:
Cell Reports, Vol 35, Iss 7, Pp 109154- (2021)
Summary: Human telomerase reverse transcriptase (hTERT) remains suppressed in most normal somatic cells. Resulting erosion of telomeres leads eventually to replicative senescence. Reactivation of hTERT maintains telomeres and triggers progression of
Externí odkaz:
https://doaj.org/article/31ab0e244fa34537a9b0a97737a04c10
Autor:
Simona Marzano, Giulia Miglietta, Rita Morigi, Jessica Marinello, Andrea Arleo, Monica Procacci, Alessandra Locatelli, Alberto Leoni, Bruno Pagano, Antonio Randazzo, Jussara Amato, Giovanni Capranico
Publikováno v:
Journal of medicinal chemistry. 65(18)
G-quadruplex (G4) ligands are investigated to discover new anticancer drugs with increased cell-killing potency. These ligands can induce genome instability and activate innate immune genes at non-cytotoxic doses, opening the discovery of cytostatic
Publikováno v:
Nucleic Acids Research
G-quadruplexes (G4s) are non-canonical nucleic acid structures involved in fundamental biological processes. As G4s are promising anticancer targets, in past decades the search for effective anticancer G4 binders aimed at the discovery of more cytoto
Autor:
Jussara Amato, Giulia Miglietta, Nunzia Iaccarino, Antonio Randazzo, Giovanni Capranico, Bruno Pagano, Alessandra Locatelli, Ettore Novellino, Alberto Leoni, Rita Morigi
Publikováno v:
Journal of Medicinal Chemistry
Targeting G-quadruplex structures is currently viewed as a promising anticancer strategy. Searching for potent and selective G-quadruplex binders, here we describe a small series of new monohydrazone derivatives designed as analogues of a lead which
G-quadruplex (G4) binders have been investigated to discover new anticancer drugs worldwide in past decades. As these ligands are generally not highly cytotoxic, the discovery rational was mainly based on increasing the cell-killing potency. Neverthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ab47719cd2e5f77ddd4dcaafaa2e8c4
https://hdl.handle.net/11585/897431
https://hdl.handle.net/11585/897431
Autor:
Bruno Pagano, Erica Salvati, Simona Marzano, Stefano De Tito, Eleonora Vertecchi, Jussara Amato, Anna Di Porzio, Nunzia Iaccarino, Antonio Randazzo
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 10315, p 10315 (2021)
International Journal of Molecular Sciences
Volume 22
Issue 19
International Journal of Molecular Sciences
Volume 22
Issue 19
DNA G-quadruplex (G4) structures, either within gene promoter sequences or at telomeres, have been extensively investigated as potential small-molecule therapeutic targets. However, although G4s forming at the telomeric DNA have been extensively inve
Autor:
Rosa Gaglione, Ettore Napolitano, Chiara Platella, Valentina Pirota, Daniela Montesarchio, Filippo Doria, Angela Arciello, Domenica Musumeci
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 10624, p 10624 (2021)
International Journal of Molecular Sciences
Volume 22
Issue 19
International Journal of Molecular Sciences
Volume 22
Issue 19
G-quadruplex existence was proved in cells by using both antibodies and small molecule fluorescent probes. However, the G-quadruplex probes designed thus far are structure- but not conformation-specific. Recently, a core-extended naphthalene diimide
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Recently, non-canonical DNA structures, such as G-quadruplexes (GQs), were found to be highly pressure sensitive, suggesting that pressure modulation studies can provide additional mechanistic details of such biomolecular systems. Using FRET and CD s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8418fe187c0a0164c5f36e54c62dc43d
http://hdl.handle.net/2003/40590
http://hdl.handle.net/2003/40590
Autor:
Shantanu Chowdhury, Antara Sengupta, Silje Lier, Meenakshi Verma, Manish Kumar, Shalu Sharma, Deo Prakash Pandey, Shuvra Shekhar Roy, Ananda Kishore Mukherjee, Gaute Nesse, Sulochana Bagri
Publikováno v:
Cell Reports, Vol 35, Iss 7, Pp 109154-(2021)
Cell reports
Cell reports
Summary Human telomerase reverse transcriptase (hTERT) remains suppressed in most normal somatic cells. Resulting erosion of telomeres leads eventually to replicative senescence. Reactivation of hTERT maintains telomeres and triggers progression of >
Autor:
Barbara Zambelli, Ilse Manet, Mauro Freccero, Giorgio Colombo, Filippo Doria, Francesco Manoli
Publikováno v:
Chemistry (Weinh., Print) 27 (2021): 11707–11720. doi:10.1002/chem.202101486
info:cnr-pdr/source/autori:Manoli, Francesco; Doria, Filippo; Colombo, Giorgio; Zambelli, Barbara; Freccero, Mauro; Manet, Ilse/titolo:The Binding Pocket at the Interface of Multimeric Telomere G-quadruplexes: Myth or Reality?/doi:10.1002%2Fchem.202101486/rivista:Chemistry (Weinh., Print)/anno:2021/pagina_da:11707/pagina_a:11720/intervallo_pagine:11707–11720/volume:27
Chemistry (Weinheim an Der Bergstrasse, Germany)
info:cnr-pdr/source/autori:Manoli, Francesco; Doria, Filippo; Colombo, Giorgio; Zambelli, Barbara; Freccero, Mauro; Manet, Ilse/titolo:The Binding Pocket at the Interface of Multimeric Telomere G-quadruplexes: Myth or Reality?/doi:10.1002%2Fchem.202101486/rivista:Chemistry (Weinh., Print)/anno:2021/pagina_da:11707/pagina_a:11720/intervallo_pagine:11707–11720/volume:27
Chemistry (Weinheim an Der Bergstrasse, Germany)
Human telomeric DNA with hundreds of repeats of the 5’‐TTAGGG‐3’ motif plays a crucial role in several biological processes. It folds into G‐quadruplex (G4) structures and features a pocket at the interface of two contiguous G4 blocks. Up t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1aada1de084a0a534794f597c8803fd5
https://hdl.handle.net/11585/856814
https://hdl.handle.net/11585/856814