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Pax3 loss of function delays tumour progression in kRAS-induced zebrafish rhabdomyosarcoma models
Umeå University, Faculty of Medicine, Department of Integrative Medical Biology (IMB).
Umeå University, Faculty of Medicine, Department of Integrative Medical Biology (IMB).ORCID iD: 0000-0002-5631-2332
Umeå University, Faculty of Medicine, Umeå Centre for Molecular Medicine (UCMM).
Umeå University, Faculty of Medicine, Umeå Centre for Molecular Medicine (UCMM).ORCID iD: 0000-0003-1283-0784
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2022 (English)In: Scientific Reports, E-ISSN 2045-2322, Vol. 12, no 1, article id 17149Article in journal (Refereed) Published
Abstract [en]

Rhabdomyosarcoma is a soft tissue cancer that arises in skeletal muscle due to mutations in myogenic progenitors that lead to ineffective differentiation and malignant transformation. The transcription factors Pax3 and Pax7 and their downstream target genes are tightly linked with the fusion positive alveolar subtype, whereas the RAS pathway is usually involved in the embryonal, fusion negative variant. Here, we analyse the role of Pax3 in a fusion negative context, by linking alterations in gene expression in pax3a/pax3b double mutant zebrafish with tumour progression in kRAS-induced rhabdomyosarcoma tumours. Several genes in the RAS/MAPK signalling pathway were significantly down-regulated in pax3a/pax3b double mutant zebrafish. Progression of rhabdomyosarcoma tumours was also delayed in the pax3a/pax3b double mutant zebrafish indicating that Pax3 transcription factors have an unappreciated role in mediating malignancy in fusion negative rhabdomyosarcoma.

Place, publisher, year, edition, pages
Nature Publishing Group, 2022. Vol. 12, no 1, article id 17149
National Category
Cancer and Oncology Medical Genetics and Genomics
Identifiers
URN: urn:nbn:se:umu:diva-203323DOI: 10.1038/s41598-022-21525-5ISI: 000867889200055PubMedID: 36229514Scopus ID: 2-s2.0-85139945677OAI: oai:DiVA.org:umu-203323DiVA, id: diva2:1728305
Available from: 2023-01-18 Created: 2023-01-18 Last updated: 2025-10-23Bibliographically approved
In thesis
1. Tumour progression and photodynamic therapy in a zebrafish model of rhabdomyosarcoma
Open this publication in new window or tab >>Tumour progression and photodynamic therapy in a zebrafish model of rhabdomyosarcoma
2025 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Rhabdomyosarcoma (RMS) is the most common pediatric soft-tissue cancer, which primarily develops in muscle tissue during childhood. Despite advances in treatment, outcomes for many patients remain poor. This thesis aims to investigate RMS progression and regression in different genetic contexts, using zebrafish RMS models to evaluate a novel molecule as a potential RMS treatment.

Pax3 and Pax7 transcription factors play important roles in fusion-positive RMS. However, their role in fusion-negative RMS remains less clear. Therefore, we aimed to examine how the lack of Pax3 and Pax7 influences fusion-negative RMS formation and progression.

In the first study, we investigated the role of Pax3 in RAS-driven, fusion-negative RMS. Using pax3a-/-;pax3b-/- double mutant zebrafish, we found that the RAS/MAPK signalling pathway was downregulated in the mutants compared to controls, correlating with a delay in tumour progression. These findings suggest that, in fusion-negative RMS, Pax3 also contributes to tumour development by modulating oncogenic signalling. 

In the second study, we aimed to explore the role of Pax7 in fusion-negative RMS, using a pax7-deficient zebrafish model. Our RNA-seq and lipidomics analyses showed downregulation of mitochondrial-related genes, decreased cardiolipin levels, and altered microtubule dynamics in pax7a-/-;pax7b-/- mutants compared to healthy wild-type fish. We also showed lower mitochondria labelling in pax7a-/-;pax7b-/- tumours compared to wild-type tumours. These findings indicate that Pax7 plays an important role in maintaining mitochondrial membrane integrity and function in healthy and tumourigenic conditions.

In the last part of the thesis, we aimed to evaluate the feasibility of photodynamic therapy using a novel photosensitizer for cancer treatment.

In the third study we designed and synthesized a heavy-atom-free light-inducible compound called dibenzothioxanthene imide (DBI), which binds to G-quadruplex (G4) DNA. Upon targeted photoactivation of DBI, it produced reactive oxygen species and caused DNA damage in human cancer cells and healthy zebrafish embryos. 

Complementing this, the last study explored the potential of photodynamic therapy using the photosensitizer DBI for treating RMS in zebrafish models. Treatment with light-activated DBI resulted in targeted apoptosis and tumour regression, compared to control treatments. In addition, RMS tissue was more affected by photoactivated DBI than healthy tissue, likely due to the higher accumulation of G4 structures in tumours compared to healthy regions.

Together, these findings uncover new roles of Pax3 and Pax7 in RMS biology using zebrafish models and highlight the therapeutic potential of G4-targeted photodynamic therapy for RMS.

Place, publisher, year, edition, pages
Umeå: Umeå University, 2025. p. 60
Series
Umeå University medical dissertations, ISSN 0346-6612 ; 2384
Keywords
rhabdomyosarcoma, zebrafish, photodynamic therapy, G-quadruplex, cancer, Pax3, Pax7
National Category
Basic Cancer Research
Identifiers
urn:nbn:se:umu:diva-245793 (URN)978-91-8070-816-6 (ISBN)978-91-8070-815-9 (ISBN)
Public defence
2025-11-20, BIO.E.203 - Aula Biologica, Biologihuset, Umeå, 09:00 (English)
Opponent
Supervisors
Available from: 2025-10-30 Created: 2025-10-23 Last updated: 2025-10-29Bibliographically approved

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Kahsay, AbrahaRodriguez-Marquez, EvaLópez-Pérez, Ana R.Hörnblad, Andreasvon Hofsten, Jonas

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