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The role of the kisspeptin receptor, KISS1R, in breast cancer cell proliferation, invasion and migration.

Dissertation (MSc)--University of Pretoria, 2021.

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Other Authors: Van den Bout, Jan Iman
Format: Thesis
Language:English
Published: University of Pretoria 2021
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access_status_str Open Access
author2 Van den Bout, Jan Iman
author_browse Van den Bout, Jan Iman
author_facet Van den Bout, Jan Iman
collection Thesis
dc_rights_str_mv © 2019 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
description Dissertation (MSc)--University of Pretoria, 2021.
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institution University of Pretoria (South Africa)
language English
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license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2021
publishDateRange 2021
publishDateSort 2021
publisher University of Pretoria
publisherStr University of Pretoria
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source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/78676 The role of the kisspeptin receptor, KISS1R, in breast cancer cell proliferation, invasion and migration. Van den Bout, Jan Iman feliciaazubuike@gmail.com Anderson, Ross Azubuike, Udochi Felicia UCTD Breast cancer KISS1R Kisspeptin receptor Cancer cell biology Tumor progression Health sciences theses SDG-03 Health sciences theses SDG-17 Health sciences theses SDG-09 Dissertation (MSc)--University of Pretoria, 2021. Kisspeptin receptor, also known as KISS1R, is the endogenous receptor for the ligand peptide, kisspeptin. It is a G-protein coupled receptor that couples through the Gαq/11 pathway. It has been shown that KISS1R activation by kisspeptin results in the activation of phospholipase C, calcium mobilization and ERK1/2 phosphorylation. Moreover, kisspeptin production has been linked to inhibition of metastasis in many cancers. However, in breast cancer, conflicting studies have shown that kisspeptin and KISS1R may play pro-metastatic or anti-metastatic roles. The aim of this study was to decipher the role of endogenous KISS1R in breast cancer cell proliferation, invasion and migration. Firstly, endogenous protein expression of the receptor was determined in 3 breast cancer cell lines by western blotting. Secondly, the signalling potential of the receptor was determined by assessing ERK1/2 phosphorylation after stimulation of cells with the ligand, KP-10. The effects of KP-10 stimulation on the growth rate and migration speed of the cell lines were assessed using crystal violet staining and scratch assay, respectively. Lastly, the last exon, exon 5 of the KISS1R gene in the BT-20 and MDA-MB-231 cell lines was assessed by Sanger sequencing. The results show that KISS1R protein is expressed in all the breast cancer cell lines tested albeit at significantly different levels. The non-metastatic BT-20 cell line express a much higher level of KISS1R compared to the metastatic MDA-MB-231 cell line or the migratory, MCF-7 cell line. Furthermore, ERK1/2 phosphorylation analysis after ligand stimulation suggests that only BT-20 cells muster a KISS1R response while no ERK1/2 phosphorylation is seen in MDA-MB-231 cells. The temporal nature of the ERK1/2 response suggests that it is a β-arrestin related activation of ERK1/2. Interestingly, β-arrestin1/2 expression analysis shows high levels of β-arrestin1/2 expression in BT-20 cells but very little in MDA-MB-231 cells. Physiologically, treatment with the KISS1R ligand, KP-10, had no significant impact on cell growth and migration. However, under serum free culture conditions, there was an increase in the migration of MDA-MB-231 cell line treated with KP-10, compared to the untreated control. In the BT-20 and MDA-MB-231 cell lines, a KISS1R variant was identified which was characterized by a c.1091T>A in exon 5, resulting in the substitution of leucine to histidine (p.L364H) in the C-terminus or cytoplasmic tail of the receptor. Overall, our data suggest that KISS1R expression correlates with the migratory potential of the cells and the KISS1R in the BT-20 cells activates ERK1/2 through a G-protein independent mechanism. NRF University of Pretoria, short-term bursary. em2026 Physiology MSc Restricted SDG-03: Good health and well-being SDG-17: Partnerships for the goals SDG-09: Industry, innovation and infrastructure 2021-02-16T06:45:05Z 2021-02-16T06:45:05Z 2021-04-16 2021-02-10 Dissertation Azubuike, UF 2021, The role of the kisspeptin receptor, KISS1R, in breast cancer cell proliferation, invasion and migration., MSc Dissertation, University of Pretoria, Pretoria, viewed yymmdd <http://hdl.handle.net/2263/78676> A2021 http://hdl.handle.net/2263/78676 en © 2019 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. application/pdf University of Pretoria
spellingShingle UCTD
Breast cancer
KISS1R
Kisspeptin receptor
Cancer cell biology
Tumor progression
Health sciences theses SDG-03
Health sciences theses SDG-17
Health sciences theses SDG-09
The role of the kisspeptin receptor, KISS1R, in breast cancer cell proliferation, invasion and migration.
title The role of the kisspeptin receptor, KISS1R, in breast cancer cell proliferation, invasion and migration.
title_full The role of the kisspeptin receptor, KISS1R, in breast cancer cell proliferation, invasion and migration.
title_fullStr The role of the kisspeptin receptor, KISS1R, in breast cancer cell proliferation, invasion and migration.
title_full_unstemmed The role of the kisspeptin receptor, KISS1R, in breast cancer cell proliferation, invasion and migration.
title_short The role of the kisspeptin receptor, KISS1R, in breast cancer cell proliferation, invasion and migration.
title_sort role of the kisspeptin receptor kiss1r in breast cancer cell proliferation invasion and migration
topic UCTD
Breast cancer
KISS1R
Kisspeptin receptor
Cancer cell biology
Tumor progression
Health sciences theses SDG-03
Health sciences theses SDG-17
Health sciences theses SDG-09
url http://hdl.handle.net/2263/78676