Zobrazeno 1 - 10
of 26
pro vyhledávání: '"S F Hoare"'
Autor:
W. Heung Chong, Richard Marais, David M. Kallenberg, S F Hoare, J. W. M. Chow, Dorothy C. Bennett, Rebecca S. Collinson, Carla Milagre, Lucy Hill, Julia K. Soo, Alastair D. MacKenzie Ross, W. Nicol Keith, Mehnaz Hossain
Publikováno v:
Pigment Cell & Melanoma Research. 24:490-503
Cell senescence is a permanent growth arrest following extended proliferation. Cultured cancer cells including metastatic melanoma cells often appear immortal (proliferate indefinitely), while uncultured benign nevi (moles) show senescence markers. H
Autor:
Claire J. Cairney, Alan Bilsland, Sharon Burns, Kyle Lafferty-Whyte, S F Hoare, William Nicol Keith, Nadia Zaffaroni
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 12, Iss 5, Pp 405-414 (2010)
Replicative senescence forms a major barrier to tumor progression. Cancer cells bypass this by using one of the two known telomere maintenance mechanisms: telomerase or the recombination-based alternative lengthening of telomeres (ALT) mechanism. The
Autor:
Chunbo Yang, Lyle Armstrong, Irina Neganova, Philip W. Hinds, W. Nicol Keith, Michael J. Cooke, Xin Zhang, Tom Strachan, Miodrag Stojkovic, Majlinda Lako, Owen Hughes, Stefan Przyborski, George Anyfantis, Stefan Fenyk, Stuart P. Atkinson, S F Hoare
Publikováno v:
The Journal of Cell Biology
In this study, we show that NANOG, a master transcription factor, regulates S-phase entry in human embryonic stem cells (hESCs) via transcriptional regulation of cell cycle regulatory components. Chromatin immunoprecipitation combined with reporter-b
Publikováno v:
British Journal of Cancer
Telomere length is maintained by two known mechanisms, activation of telomerase or alternative lengthening of telomeres (ALT). The ALT pathway is more commonly activated in tumours of mesenchymal origin, although the mechanisms involved in the decisi
Publikováno v:
Serakinci, N, Hoare, S F, Kassem, M, Atkinson, S P & Keith, W N 2006, ' Telomerase promoter reprogramming and interaction with general transcription factors in the human mesenchymal stem cell ', Regenerative Medicine, vol. 1, no. 1, pp. 125-131 . https://doi.org/10.2217/17460751.1.1.125
Udgivelsesdato: Jan The human adult mesenchymal stem cell (hMSC) does not express telomerase and has been shown to be the target for neoplastic transformation after transduction with hTERT. These findings lend support to the stem cell hypothesis of c
Publikováno v:
Oncogene. 25:61-69
Basal telomerase activity is dependent on expression of the hTERT and hTR genes and upregulation of telomerase gene expression is associated with tumour development. It is therefore possible that signal transduction pathways involved in tumour develo
Publikováno v:
Cancer Research. 65:7585-7590
The presence of active telomere maintenance mechanisms in immortal cells allows the bypass of senescence by maintaining telomere length. In most immortal cell lines and tumors, telomere maintenance is attributable to telomerase reactivation. However,
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 7, Iss 6, Pp 614-622 (2005)
Telomerase plays a role in the unlimited replicative capacity of the majority of cancer cells and provides a potential anticancer target. The regulation of telomerase is complex but transcriptional control of its two essential components, hTERC (RNA
Autor:
Andrew Protheroe, David Propper, Barry W. Hancock, Cheng Han, Srinivasan Madhusudan, Frances R. Balkwill, Adrian L. Harris, Helena M. Earl, Paul A. Vasey, Pippa Corrie, A Turner, S F Hoare
Publikováno v:
British Journal of Cancer
Protein kinase C (PKC) has a critical role in several signal transduction pathways, and is involved in renal cancer pathogenesis. Bryostatin-1 modulates PKC activity and has antitumour effects in preclinical studies. We conducted a multicentre phase
Publikováno v:
FEBS Letters. 536:111-119
The proximal promoter of the telomerase RNA gene, hTR, contains four Sp1 sites and one CCAAT box. We have carried out a functional analysis of the role of these sequence elements. Two Sp1 sites downstream of the CCAAT box mediated negative regulation