Literature DB >> 19003245

Targeting human telomerase for cancer therapeutics.

Lionel Guittat1, Patrizia Alberti, Dennis Gomez, Anne De Cian, Gaëlle Pennarun, Thibault Lemarteleur, Chafke Belmokhtar, Rajaa Paterski, Hamid Morjani, Chantal Trentesaux, Eliane Mandine, François Boussin, Patrick Mailliet, Laurent Lacroix, Jean-François Riou, Jean-Louis Mergny.   

Abstract

The enzyme telomerase is involved in the replication of telomeres, specialized structures that cap and protect the ends of chromosomes. Its activity is required for maintenance of telomeres and for unlimited lifespan, a hallmark of cancer cells. Telomerase is overexpressed in the vast majority of human cancer cells and therefore represents an attractive target for therapy. Several approaches have been developed to inhibit this enzyme through the targeting of its RNA or catalytic components as well as its DNA substrate, the single-stranded 3'-telomeric overhang. Telomerase inhibitors are chemically diverse and include modified oligonucleotides as well as small diffusable molecules, both natural and synthetic. This review presents an update of recent investigations pertaining to these agents and discusses their biological properties in the context of the initial paradigm that the exposure of cancer cells to these agents should lead to progressive telomere shortening followed by a delayed growth arrest response.

Entities:  

Year:  2004        PMID: 19003245      PMCID: PMC3449961          DOI: 10.1007/s10616-004-5127-z

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  135 in total

1.  Inhibition of telomerase by G-quartet DNA structures.

Authors:  A M Zahler; J R Williamson; T R Cech; D M Prescott
Journal:  Nature       Date:  1991-04-25       Impact factor: 49.962

2.  Telomere shortening and growth inhibition of human cancer cells by novel synthetic telomerase inhibitors MST-312, MST-295, and MST-1991.

Authors:  Hiroyuki Seimiya; Tomoko Oh-hara; Tsuneji Suzuki; Imad Naasani; Toshiyuki Shimazaki; Katsutoshi Tsuchiya; Takashi Tsuruo
Journal:  Mol Cancer Ther       Date:  2002-07       Impact factor: 6.261

3.  Quadruplex-interactive agents as telomerase inhibitors: synthesis of porphyrins and structure-activity relationship for the inhibition of telomerase.

Authors:  D F Shi; R T Wheelhouse; D Sun; L H Hurley
Journal:  J Med Chem       Date:  2001-12-20       Impact factor: 7.446

4.  Reverse transcriptase inhibitors suppress telomerase function and induce senescence-like processes in cultured mouse fibroblasts.

Authors:  Y E Yegorov; D N Chernov; S S Akimov; N L Bolsheva; A A Krayevsky; A V Zelenin
Journal:  FEBS Lett       Date:  1996-07-01       Impact factor: 4.124

5.  Allosteric inhibitors of telomerase: oligonucleotide N3'-->P5' phosphoramidates.

Authors:  Ronald Pruzan; Krisztina Pongracz; Kimberly Gietzen; Gerald Wallweber; Sergei Gryaznov
Journal:  Nucleic Acids Res       Date:  2002-01-15       Impact factor: 16.971

6.  hEST2, the putative human telomerase catalytic subunit gene, is up-regulated in tumor cells and during immortalization.

Authors:  M Meyerson; C M Counter; E N Eaton; L W Ellisen; P Steiner; S D Caddle; L Ziaugra; R L Beijersbergen; M J Davidoff; Q Liu; S Bacchetti; D A Haber; R A Weinberg
Journal:  Cell       Date:  1997-08-22       Impact factor: 41.582

7.  Effects of oligonucleotide N3'-->P5' thio-phosphoramidate (GRN163) targeting telomerase RNA in human multiple myeloma cells.

Authors:  Masaharu Akiyama; Teru Hideshima; Masood A Shammas; Toshiaki Hayashi; Makoto Hamasaki; Yu-Tzu Tai; Paul Richardson; Sergei Gryaznov; Nikhil C Munshi; Kenneth C Anderson
Journal:  Cancer Res       Date:  2003-10-01       Impact factor: 12.701

8.  Specific interactions of distamycin with G-quadruplex DNA.

Authors:  Melanie J Cocco; L A Hanakahi; Michael D Huber; Nancy Maizels
Journal:  Nucleic Acids Res       Date:  2003-06-01       Impact factor: 16.971

9.  Telomerase inhibition with an oligonucleotide telomerase template antagonist: in vitro and in vivo studies in multiple myeloma and lymphoma.

Authors:  Eunice S Wang; Kaida Wu; Allison C Chin; Selina Chen-Kiang; Krisztina Pongracz; Sergei Gryaznov; Malcolm A S Moore
Journal:  Blood       Date:  2003-09-11       Impact factor: 22.113

10.  Consequences of telomerase inhibition and combination treatments for the proliferation of cancer cells.

Authors:  Zhi Chen; Kenneth S Koeneman; David R Corey
Journal:  Cancer Res       Date:  2003-09-15       Impact factor: 12.701

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  5 in total

1.  DNA adducts of antitumor cisplatin preclude telomeric sequences from forming G quadruplexes.

Authors:  Pavla Heringova; Jana Kasparkova; Viktor Brabec
Journal:  J Biol Inorg Chem       Date:  2009-04-24       Impact factor: 3.358

2.  RNA interference mediated downregulation of human telomerase reverse transcriptase (hTERT) in LN18 cells.

Authors:  Ch Lavanya; M K Sibin; M M Srinivas Bharath; M Jeru Manoj; Manjunatha M Venkataswamy; Dhananjaya I Bhat; K V L Narasinga Rao; G K Chetan
Journal:  Cytotechnology       Date:  2016-10-18       Impact factor: 2.058

Review 3.  Development of anticancer drugs based on the hallmarks of tumor cells.

Authors:  Natalia Bailón-Moscoso; Juan Carlos Romero-Benavides; Patricia Ostrosky-Wegman
Journal:  Tumour Biol       Date:  2014-01-29

4.  Preferential binding of a G-quadruplex ligand to human chromosome ends.

Authors:  Christine Granotier; Gaëlle Pennarun; Lydia Riou; Françoise Hoffschir; Laurent R Gauthier; Anne De Cian; Dennis Gomez; Eliane Mandine; Jean-François Riou; Jean-Louis Mergny; Patrick Mailliet; Bernard Dutrillaux; François D Boussin
Journal:  Nucleic Acids Res       Date:  2005-07-28       Impact factor: 16.971

5.  Construction of a transcription factor‑long non‑coding RNA‑microRNA network for the identification of key regulators in lung adenocarcinoma and lung squamous cell carcinoma.

Authors:  Shuai Zhao; Hong Chen; Beichen Ding; Jianing Li; Fuzhen Lv; Kaiyu Han; Dan Zhou; Baiquan Yu; Yao Yu; Wei Zhang
Journal:  Mol Med Rep       Date:  2018-12-14       Impact factor: 2.952

  5 in total

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