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Omics · dataset · 2026

Bioinformatics-driven insights into the role of cathepsins in tumour biology

Listed in ZivaHub and Deakin Research Online and DMU Figshare — shown once because both records carry DOI 10.17034/32805359.v1

<div>Cysteine cathepsins are proteolytic enzymes implicated in cancer progression through their involvement in tumour growth, extracellular matrix (ECM) remodelling, and modulation of the tumour microenvironment (TME).

Description

This thesis examines the molecular roles of two cysteine cathepsins, cathepsin S (CTSS) and cathepsin V (CTSV), with a focus on their relevance to breast cancer biology and disease aggressiveness.</div><div>Using bioinformatic approaches, CTSS expression was examined across a range of malignancies, where elevated expression was associated with features of aggressive disease.

Further analyses identified links between CTSS expression patterns and cellular responses to genomic stress. Complementary <i>in vitro </i>experiments demonstrated that genotoxic stress conditions can modulate CTSS expression in breast cancer cell models and influence invasive cellular behaviours, supporting a functional role for CTSS in tumour progression. These findings suggest that CTSS activity is responsive to perturbations in genome maintenance pathways, although the precise regulatory mechanisms require further investigation.</div><div>This thesis also explores the role of CTSV in breast cancer.

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Transcriptomic analyses indicated associations between CTSV expression and pathways involved in cell proliferation and phenotypic plasticity. Functional studies revealed that modulation of CTSV expression produces context-dependent effects across breast cancer subtypes, highlighting heterogeneity in cathepsin-mediated signalling and tumour behaviour.</div><div>Overall, this work advances understanding of the involvement of CTSS and CTSV in breast cancer and underscores the complexity of protease regulation in oncogenic contexts.

The findings support the potential relevance of cysteine cathepsins as biomarkers and therapeutic targets, while providing a platform for future studies aimed at clarifying their clinical significance and mechanistic roles in cancer progression.</div><br><i>Thesis embargoed until 31st July 2031</i>

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Inferred from text
Disease 75% · Molecular targets 76%
Provenance · 3 source records, 19 field assertions
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ZivaHuboai:figshare.com:article/328053595 d agoJSON v1
Deakin Research Onlineoai:figshare.com:article/328053595 d agoJSON v1
DMU Figshareoai:figshare.com:article/328053595 d agoJSON v1
FieldAssertionExtractorEvidence
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concepts[disease].local:disease:cancermapping · figshare dmu ac ukvocabulary-mapper@1.0.0keywords['cancer']
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concepts[modality].local:modality:rna-seqmapping · zivahub uct ac zavocabulary-mapper@1.0.0keywords['RNA-sequencing']
concepts[modality].local:modality:rna-seqmapping · dro deakin edu auvocabulary-mapper@1.0.0keywords['RNA-sequencing']
concepts[modality].local:modality:rna-seqmapping · figshare dmu ac ukvocabulary-mapper@1.0.0keywords['RNA-sequencing']
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