Dr McFarlane’s group is interested in how cancer cells utilise germline / stem cell genes to control cell proliferation and genome dynamics. They are particularly interested in genes that regulate genome stability and cell division. His team not only works with human cancer cells and model organisms, but they also use human embryo stem cells and induced pluripotent stem cells. The ultimate aim of their work is to contribute insight to enable them to develop new diagnostic and patient stratification technologies and to identify and exploit new anti-cancer drug targets.

Impact

Dr McFarlane has served as a full member of the North West Cancer Research Committee for 5 years. He has reviewed regularly for international funding bodies and journals and has served as external Ph.D. examiner for a large number of national and international institutions.

‘’My research is aimed at ultimately benefitting cancer suffers and I chose to come to Bangor University for the unique opportunities it offered.’’

Previous University Positions

Lecturer / Project manager – North West Cancer Research Institute

Other external positions currently held

Visiting Professor – King Saud University, Saudi Arabia

Other external positions previously held

Visiting Scientist – CABIMER Institute for Regenerative Medicine, Sevilla, Spain

NIH Postdoctoral Fellow, Fred Hutchinson Cancer Research Center, Seattle, USA

MRC Research associate, Krebs Institute, University of Sheffield

Educational Background

Ph.D. Medical Genetics (Prof. John Saunders), Liverpool University, UK

Location: Brambell, Room 405

Phone: 2360

Email: r.macfarlane@bangor.ac.uk

Position: Senior Lecturer / Research Group Leader / Deputy Head of School – Research

Dr McFarlane’s previous research has been aimed at understanding how complex organisms, such as humans, regulate and maintain genetic stability to avoid genetic disease such as cancer. Key findings in his group include the discovery that the mechanism that drives most caners, failures in DNA replication, does not occur uniformly throughout the genome (e.g., Pryce et al. 2009 Proc. Natl. Acad. Sci. USA 106, 4770-4775) and, more recently, that a highly conserved set of proteins control the terminal regions, the telomeres, which are important in cancer progression and human aging (Gomez-Escobar et al. 2016 Oncotarget in press). They have extended their work to identify a large cohort of new cancer biomarker genes (e.g., Feichtinger et al. 2012 Oncotarget 3, 843-853; Feichtinger et al. 2014 Int. J. Cancer 134, 2359-2365) and are currently exploring ways in which the products of these genes can be used for the development of new drug targets.

Practical applications/impact of findings to date

We have identified a large number of cancer-specific genes. These can be exploited in a number of way. Firstly, their expression profile can be used to stratify patients to select therapeutic strategies. Secondly, they have great potential in the development of early diagnostic technologies. Thirdly, they provide unique therapeutic targets, including direct drug targets and targets for immunotherapeutic based strategies. Additionally, we have developed computational tools that enable the wider community to explore the cancer specificity of groups of genes they may be working on in a more systematic fashion (e.g., Feichtinger 2012 et al. Database 2012 bas055).

Funding and key grants

His group has been funded by significant awards from the following organisations: MRC, WORD (NISCHR), Wellcome Trust, Royal Society, BBSRC, North West Cancer Research, Cancer Research Wales, NHS, Saudi Arabian Government.

Facilities

Most of the equipment used within Dr McFarlane’s group has been funded directly by externally won awards. These include: human cancer cell / embryo stem cell tissue culture suit, confocal microscopes, fluorescence activated cell sorting, fluorescence microscopes, phosphorimagers and a range of basic molecular biology technologies (RT-qPCR).

Strengths

On arriving at Bangor I established the North West Cancer Research Institute in collaboration with the regional cancer charity, North West Cancer Research. This has resulted in a dedicated group of research team leaders in Bangor with a focus aimed at understanding genome dynamics in cancer. These teams, and the associated, technology base, make this an excellent place to conduct cancer research within Wales. We are also part of wider Welsh and North West regional cancer research networks.

Keywords

Germ line genes, Cancer testis antigens, meiosis, telomeres, gene stability, embryo stem cells, cancer stem-like cells.

2022

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2020

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2019

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2017

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2016

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2015

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2014

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2013

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2012

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2010

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2009

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2008

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2007

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2006

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2005

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2004

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2002

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1998

• CyhoeddwydModification of bacterial artificial chromosomes through chi-stimulated homologous recombination and its application in zebrafish transgenesis.
  Jessen, J. R., Meng, A., Mcfarlane, R., Paw, B. H., Zon, L. I., Smith, G. R. & Lin, S., 1998, Yn: Proceedings of the National Academy of Sciences of the USA. 95, 9, t. 5121 5126 t.
  Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid

1997

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1996

• Cyhoeddwyd5-azacytidine treatment of the fission yeast leads to cytotxicity and cell cycle arrest.
  Taylor, E. M., Mcfarlane, R. & Price, C., 1996, Yn: Molecular Genetics and Genomics. 253, 1-2, t. 128-137
  Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid
• CyhoeddwydMolecular mechanisms of intramolecular recombination-dependent recircularization of linearized plasmid DNA in Escherichia coli: requirements for ruvA, ruvB, recG, recF and recR gene products.
  Mcfarlane, R. & Saunders, J. R., 1996, Yn: Gene. 177, 1-2, t. 209-216
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• TBC

  01/09/2021 – 31/08/2022 (Wrthi'n gweithredu)

• Financial support to amend an existing funded research program in order to allow a trainee oncologist to provide clinical service

  01/12/2020 – 30/11/2023 (Wrthi'n gweithredu)

• KESS II Phd with Carl Zeiss Ltd - BUK2173

  01/11/2018 – 30/07/2022 (Wedi gorffen)

• KESS II Phd with Awyr Las- BUK2171

  01/10/2018 – 15/08/2022 (Wedi gorffen)

• Role of TEX19 in tumour growth & progression

  01/10/2015 – 31/07/2016 (Wedi gorffen)

  Cysylltau:

  • https://www.bangor.ac.uk/research/news/a-human-stem-cell-specific-gene-usually-only-active-in-the-testis-can-influence-cancer-cell-proliferation-and-prognosis-in-a-wide-range-of-different-cancers-32454

• Genomic scale analysis of germ line genes.

  01/08/2013 – 31/10/2015 (Wedi gorffen)

• The meiCT genes in colorectal and ovarian cancer

  01/01/2013 – 31/12/2015 (Wedi gorffen)

• A pilot study into the validation and identification of a new family of oncogenes.

  09/05/2011 – 08/01/2013 (Wedi gorffen)

• Identification and functional characterisation of novel cancer testis antigens for cancer therapy and diagnosis

  01/12/2009 – 01/07/2011 (Wedi gorffen)

• Identification and analysis of new cancer testis antigens for use in novel diagnostic and therapeutic technologies

  01/10/2009 – 25/06/2013 (Wedi gorffen)

• Function Of The Leukaemia-Associated

  01/12/2007 – 31/07/2009 (Wedi gorffen)

• Assessment Of A Sub Group Of Non-X Cancr

  24/09/2007 – 30/09/2010 (Wedi gorffen)

• North Wales Stem Cell Technology Platfor

  01/01/2007 – 31/07/2010 (Wedi gorffen)

• Nwcrf- Cancer Research Institute

  01/04/2003 – 31/10/2012 (Wedi gorffen)

  Cysylltau:

  • https://www.bangor.ac.uk/medical-sciences/cancer-research.php.en