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Understanding the functions and interactions of the deubiquitinating enzyme USP7 in colorectal cancer

Understanding the functions and interactions of the deubiquitinating enzyme USP7 in colorectal cancer
Understanding the functions and interactions of the deubiquitinating enzyme USP7 in colorectal cancer
Ubiquitin-specific protease (USP7) is an oncogene that is involved in many tumour types including colorectal cancer by dysregulating various cellular pathways such as canonical Wnt signalling and the P53-MDM2 pathway. Discovering novel USP7 interacting partners can reveal the implications for the role of USP7 in other pathways and new biological functions. Therefore, USP7 becomes a promising target for cancer therapy. In this work, knocked-down USP7 colorectal cancer cells (LS188) were used as a cell model and liquid chromatography mass spectrometry was performed. We found that USP7 knockdown significantly inhibited colorectal cancer cell viability, colony formation, cell cycle and cell adhesion. The effect of USP7 Knockdown and inhibition on cell viability has been studied in both two-dimensional (2D) and three-dimensional culture (3D). The impact on the cell cycle in USP7 inhibited or depleted cells was p53 independent. The novelty in our study is that we found that protein expression of Ajuba LIM domain protein was reduced upon USP7 depletion by shRNA or siRNA as well as inhibition with FT671 inhibitor. This reduction of Ajuba protein levels was confirmed using immunofluorescence confocal microscopy. Co-immunoprecipitation revealed that USP7 is associated with Ajuba in vitro while Knocking down Ajuba does not affect USP7 expression. Moreover, quantitative PCR analysis showed that USP7 does not affect Ajuba mRNA levels meaning that USP7 plays a role in the post-transcriptional of Ajuba. Our findings underline the functions and oncogenic roles of USP7 through its protein interaction networks and that Ajuba is one of the USP7 protein networks present in colorectal cancer.
University of Southampton
Aleidan, Ahood Abdulaziz A
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Aleidan, Ahood Abdulaziz A
e332ecb1-e877-4b7a-a501-045202f27ad1
Ewing, Robert
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Wang, Yihua
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Skipp, Paul
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Tavassoli, Ali
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Aleidan, Ahood Abdulaziz A (2023) Understanding the functions and interactions of the deubiquitinating enzyme USP7 in colorectal cancer. University of Southampton, Doctoral Thesis, 214pp.

Record type: Thesis (Doctoral)

Abstract

Ubiquitin-specific protease (USP7) is an oncogene that is involved in many tumour types including colorectal cancer by dysregulating various cellular pathways such as canonical Wnt signalling and the P53-MDM2 pathway. Discovering novel USP7 interacting partners can reveal the implications for the role of USP7 in other pathways and new biological functions. Therefore, USP7 becomes a promising target for cancer therapy. In this work, knocked-down USP7 colorectal cancer cells (LS188) were used as a cell model and liquid chromatography mass spectrometry was performed. We found that USP7 knockdown significantly inhibited colorectal cancer cell viability, colony formation, cell cycle and cell adhesion. The effect of USP7 Knockdown and inhibition on cell viability has been studied in both two-dimensional (2D) and three-dimensional culture (3D). The impact on the cell cycle in USP7 inhibited or depleted cells was p53 independent. The novelty in our study is that we found that protein expression of Ajuba LIM domain protein was reduced upon USP7 depletion by shRNA or siRNA as well as inhibition with FT671 inhibitor. This reduction of Ajuba protein levels was confirmed using immunofluorescence confocal microscopy. Co-immunoprecipitation revealed that USP7 is associated with Ajuba in vitro while Knocking down Ajuba does not affect USP7 expression. Moreover, quantitative PCR analysis showed that USP7 does not affect Ajuba mRNA levels meaning that USP7 plays a role in the post-transcriptional of Ajuba. Our findings underline the functions and oncogenic roles of USP7 through its protein interaction networks and that Ajuba is one of the USP7 protein networks present in colorectal cancer.

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Published date: 15 May 2023

Identifiers

Local EPrints ID: 477035
URI: http://eprints.soton.ac.uk/id/eprint/477035
PURE UUID: 80c5307f-fa27-4f4a-b24d-a72a764077b5
ORCID for Ahood Abdulaziz A Aleidan: ORCID iD orcid.org/0000-0001-9051-9639
ORCID for Robert Ewing: ORCID iD orcid.org/0000-0001-6510-4001
ORCID for Yihua Wang: ORCID iD orcid.org/0000-0001-5561-0648
ORCID for Paul Skipp: ORCID iD orcid.org/0000-0002-2995-2959
ORCID for Ali Tavassoli: ORCID iD orcid.org/0000-0002-7420-5063

Catalogue record

Date deposited: 24 May 2023 16:34
Last modified: 20 Mar 2024 02:48

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Contributors

Thesis advisor: Robert Ewing ORCID iD
Thesis advisor: Yihua Wang ORCID iD
Thesis advisor: Paul Skipp ORCID iD
Thesis advisor: Ali Tavassoli ORCID iD

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