4.4 Article

ERK5 and its role in tumour development

Journal

BIOCHEMICAL SOCIETY TRANSACTIONS
Volume 40, Issue -, Pages 251-256

Publisher

PORTLAND PRESS LTD
DOI: 10.1042/BST20110663

Keywords

angiogenesis; cancer; extracellular-signal-regulated kinase 5 (ERK5); microRNA (miRNA); migration; oncogene

Funding

  1. Babraham Institute
  2. Biotechnology and Biological Sciences Research Council
  3. Association for International Cancer Research and Cancer Research UK
  4. Association for International Cancer Research
  5. Biotechnology and Biological Sciences Research Council [BBS/E/B/0000H242, BB/C509190/1] Funding Source: researchfish
  6. BBSRC [BBS/E/B/0000H242] Funding Source: UKRI

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The MEK5 [MAPK (mitogen-activated protein kinase)/ERK (extracellular-signal-regulated kinase) kinase 5]/ERK5 pathway is the least well studied MAPK signalling module. It has been proposed to play a role in the pathology of cancer. In the present paper, we review the role of the MEK5/ERK5 pathway using the 'hallmarks of cancer' as a framework and consider how this pathway is deregulated. As well as playing a key role in endothelial cell survival and tubular morphogenesis during tumour neovascularization, ERK5 is also emerging as a regulator of tumour cell invasion and migration. Several oncogenes can stimulate ERK5 activity, and protein levels are increased by a novel amplification at chromosome locus 17p11 and by down-regulation of the microRNAs miR-143 and miR-145. Together, these finding underscore the case for further investigation into understanding the role of ERK5 in cancer.

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