Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Mitchell Revill"'
Autor:
Maximilian W. Schenk, Sam Humphrey, A. S. Md Mukarram Hossain, Mitchell Revill, Sarah Pearsall, Alice Lallo, Stewart Brown, Samuel Bratt, Melanie Galvin, Tine Descamps, Cong Zhou, Simon P. Pearce, Lynsey Priest, Michelle Greenhalgh, Anshuman Chaturvedi, Alastair Kerr, Fiona Blackhall, Caroline Dive, Kristopher K. Frese
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
The emergence of acquired resistance to standard platinum-etoposide chemotherapy in small cell lung cancer (SCLC) is a common event. Here, the authors using paired pre-treatment and post-chemotherapy circulating tumour cell patient-derived explant (C
Externí odkaz:
https://doaj.org/article/a99beedee95f4504bd782063edbc7711
Autor:
Francesca Trapani, Matthew G Krebs, Alastair R.W. Kerr, Adi F. Gazdar, Fiona H Blackhall, Kristopher K. Frese, William Rowe, Nicole Simms, Simon P. Pearce, Laura Booth, Mitchell Revill, Lynsey Priest, Caroline Dive, Derrick Morgan, Luc Girard, Louise Carter, Marek Dynowski, Melanie Galvin, Ruth A Stoney, Kathryn Simpson, Mathew Carter, Thomas Helps, Natalie Cook, Daisuke Nonaka, Alessia Catozzi, Sam Humphrey
Publikováno v:
Nature Cancer. 1:437-451
Although small cell lung cancer (SCLC) is treated as a homogeneous disease, biopsies and preclinical models reveal heterogeneity in transcriptomes and morphology. SCLC subtypes were recently defined by neuroendocrine transcription factor (NETF) expre
Autor:
Alessia Catozzi, Mitchell Revill, Jordan Roebuck, Sam Humphrey, Melanie Galvin, Fiona Blackhall, Kathryn Simpson, Alastair Kerr, Kristopher Frese, Caroline Dive
Publikováno v:
Cancer Research. 82:2360-2360
SCLC is an aggressive neuroendocrine (NE) cancer with a 7% 5-year survival rate. SCLC is treated as a clinically homogenous disease, but evidence of its intra- and inter-tumor heterogeneity is increasing. This is partly attributed to expression of ne
Autor:
Kristopher K. Frese, Derrick Morgan, Sam Humphrey, Mitchell Revill, Kathryn Simpson, Sarah M. Pearsall, Mathew Carter, Caroline Dive, Fiona H Blackhall, Lynsey Priest, Alistair Kerr, Melanie Galvin
Publikováno v:
Journal of Thoracic Oncology
Introduction Recent consensus defines four SCLC subtypes on the basis of transcription factor expression: ASCL1, NEUROD1, POU2F3, and YAP1. The rare YAP1 subtype is associated with “neuroendocrine (NE)-low” cells among SCLC cell lines and patient
Autor:
Derrick Morgan, Lynsey Priest, Stewart Brown, Kristopher K. Frese, Fiona H Blackhall, Mitchell Revill, Caroline Dive, Sheila K. Singh, Melanie Galvin, Maria Peiris-Pagès, Kathryn Simpson, Mathew Carter
Publikováno v:
Cancer Research. 81:2874-2874
Small cell lung cancer (SCLC) accounts for about 13% of all malignant lung tumors and is characterized by an extremely low survival rate and widespread early dissemination. Over two-thirds of SCLC patients are diagnosed with metastases in multiple or
Abstract 2436: Heterogeneity of neurogenic transcription factor expression in small cell lung cancer
Autor:
Mitchell Revill, Kristopher K. Frese, Fiona H Blackhall, Kathryn Simpson, Alessia Catozzi, Caroline Dive
Publikováno v:
Cancer Research. 81:2436-2436
SCLC is an aggressive neuroendocrine (NE) cancer with a 7% 5-year survival rate. Molecular characterization of this disease has lagged behind other cancer types and standard of care treatment has remained largely unchanged for over three decades. SCL
Autor:
Stephen Green, Armelle Logie, Nichola Whalley, Nicola Curtis, Kate Byth, Haihong Zhong, Clare Murray, Mike Firth, Lorna Hopcroft, Lorraine Mooney, Filippos Michopoulos, Paul D. Smith, Amanda Benjamin, Mitchell Revill, Susan E. Critchlow
Publikováno v:
Oncotarget
// Nicola J. Curtis 1 , Lorraine Mooney 1 , Lorna Hopcroft 2 , Filippos Michopoulos 1 , Nichola Whalley 2 , Haihong Zhong 3 , Clare Murray 4,6 , Armelle Logie 1 , Mitchell Revill 1 , Kate F. Byth 5 , Amanda D. Benjamin 4 , Mike A. Firth 1 , Stephen G
Autor:
Anna Staniszewska, Paul Lyne, Lyndsey Hanson, Linda K. Buckett, Claire Rooney, Sanjay K. Pandey, David C. Blakey, Kevin Hudson, Alexey S. Revenko, Sarah Ross, A. Robert MacLeod, Mitchell Revill, Brett P. Monia, Stephanie Klein, Michael Zinda, Rebecca Ellston, Nicky Whalley
Publikováno v:
Science Translational Medicine. 9
Activating mutations in KRAS underlie the pathogenesis of up to 20% of human tumors, and KRAS is one of the most frequently mutated genes in cancer. Developing therapeutics to block KRAS activity has proven difficult, and no direct inhibitor of KRAS
Autor:
Brett P. Monia, Sarah Ross, Mitchell Revill, Stephanie Klein, Alexey S. Revenko, Rebecca Ellston, Allan R. MacLeod, Lyndsey Hanson, David C. Blakey, Linda K. Buckett, Paul Lyne, Chris May, Kevin Hudson, Sanjay K. Pandey
Publikováno v:
Molecular Cancer Therapeutics. 14:PR12-PR12
KRAS is one of the most frequently mutated genes in cancer and its activation is thought to underlie the pathogenesis of up to 30% of all human tumors. However, to date KRAS has proven difficult to target with traditional pharmacologic approaches. An
Autor:
Liang Xie, Jingchuan Zhang, Lorraine Mooney, Nicola Curtis, De-Hua Yu, Haihong Zhong, Clare Murray, Paul D. Smith, Nicky Whalley, Armelle Logie, Lorna Hopcroft, Susan E. Critchlow, Mitchell Revill
Publikováno v:
Cancer Research. 72:3224-3224
Introduction - The metabolic phenotype of tumours (relative to most normal tissues) is shifted from oxidative phosphorylation to aerobic (Warburg Effect) or anaerobic glycolysis. This enables tumours to meet their energetic and biosynthetic demands e