The role of PKC and PKD in CXCL12 directed prostate cancer migration

Hamshaw, Isabel ORCID: https://orcid.org/0000-0001-6445-0738, Ajdarirad, Morvarid and Mueller, Anja ORCID: https://orcid.org/0000-0003-0774-0434 (2019) The role of PKC and PKD in CXCL12 directed prostate cancer migration. Biochemical and Biophysical Research Communications, 519 (1). pp. 86-92. ISSN 0006-291X

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Abstract

Cancer metastasis is the cause of most cancer related deaths and many cancers are becoming resistant to current therapies. An alternative approach is to investigating signalling pathways that cause cancer cell migration such as chemokine signalling pathways. Such downstream signalling proteins are PKC and PKD. Therefore, we investigated the role of these two proteins in CXCL12 mediated PC3 prostate cancer migration. Whereas PKC and PKD inhibitors do not affect the release of calcium in PC3 prostate cancer cells, both are involved in migration, particularly inhibition of the atypical PKC isoform PKCζ causes the greatest reduction in PC3 cell migration. Classical and/or Novel PKC isoform inhibition changes the shape of the PC3 cells, they show a more rounded morphology, whereas PKD inhibition causes prostate cancer cell to elongate. PKCζ inhibition causes the enlargement of PC3 area possibly due to dysregulated actin cytoskeletal control. These results highlight the importance of verifying which signalling proteins, in which cell and in which chemokine signalling cascade enable cancer cellular migration.

Item Type:	Article
Uncontrolled Keywords:	sdg 3 - good health and well-being ,/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being
Faculty \ School:	Faculty of Science > School of Pharmacy
UEA Research Groups:	Faculty of Science > Research Groups > Molecular and Tissue Pharmacology
Depositing User:	LivePure Connector
Date Deposited:	27 Aug 2019 14:35
Last Modified:	04 Mar 2024 17:50
URI:	https://ueaeprints.uea.ac.uk/id/eprint/72055
DOI:	10.1016/j.bbrc.2019.08.134

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