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The zebrafish as a model to elucidate human diseases and development

thesis
posted on 2024-09-03, 04:38 authored by Samantha Lee

This thesis explores the zebrafish as a model organism to illuminate our understanding of processes that orchestrate the progression of cancer metastasis and myogenesis.

First, I describe the successful establishment of a cancer metastasis model in the zebrafish, specifically to study intravasation - one of the earliest steps in the metastatic cascade. Fluorescently labeled tumour cell are transplanted into pervitelline space of 2 days post fertilisation (dpf) zebrafish embryos before they are exposed to normoxic or hypoxic conditions, allowing us to study the effect of hypoxia on tumour-induced angiogenesis and metastasis. Hypoxia elicited an enhanced angiogenic response and neovascularisation to the transplanted tumour and escalated the extent of metastasis in the living zebrafish embryo. Loss of function experiments such as vascular endothelial growth factor (VEGF) blockade using a clinically available drug – Sunitinib or VEGF morpholino knockdown attenuated tumour-induced angiogenesis and metastasis. The in vivo metastasis assay in zebrafish delivers numerous unique advantages over conventional in vitro cell-based or biochemical chemotaxis assays. The transparent embryo facilitates the tracking of the entire intravasation process in real time within a living organism, allowing us to explore the dynamic interplay of tumour cells and the environmental cues that drive metastasis. This model can be further employed to discriminate between tumour cells of different metastatic potential and to identify novel factors that present as impetus for the earliest step of the metastatic cascade.

Next, I demonstrate the analysis of one class of motility mutants originally identified in the 1996 Tübingen genetic screen that potentially serve as models for human myopathies and dystrophies. Two of these mutants have previously been cloned and shown to encode proteins involved in muscle fibre attachment whilst a third has been found to encode the molecular chaperone Heat shock protein (HSP) 90. I describe the phenotypic and molecular characterization of another of these zebrafish motility mutants, frozen (fro). I present evidence that the frot027c mutation disrupts the locus encoding the autophagy pathway component Atg10. This analysis implicates Atg10 in the assembly of both skeletal and cardiac muscle fibers suggesting a previously uncharacterized role for the autophagy pathway in this process.

Together, my findings illustrate the utility of the zebrafish as a model organism that complements established mammalian and invertebrate models. The fecundity and amenability of the zebrafish to genetic manipulation together with the rapid development and translucency of its embryos combine to provide a powerful system with which to unravel and inform the underlying mechanisms that govern fundamental biological processes and shed light on our understanding of human development and diseases.

List of scientific papers

I. Samantha Lin Chiou Lee, Pegah Rouhi, Lasse Jensen, Danfang Zhang, Hong Ji, Giselbert Hauptmann, Philip Ingham and Yihai Cao. Hypoxia-induced pathological angiogenesis mediates tumor cell dissemination, invasion, and metastasis in a zebrafish tumor model. Proc Natl Acad Sci U S A. Nov 17 2009; 106:46, 19485-90.
https://doi.org/10.1073/pnas.0909228106

II. Pegah Rouhi*, Samantha Lin Chiou Lee*, Ziquan Cao, Eva Hedlund, Lasse Jensen and Yihai Cao. Pathological angiogenesis facilitates tumor cell dissemination and metastasis. Cell Cycle. Mar 1 2010; 9:5, 913-7. *Co-first author.
https://doi.org/10.4161/cc.9.5.10853

III. Samantha Lin Chiou Lee, Sarah Baxendale, Stephen Moore, Ng Chee Peng, Tan Swee Chuan and Philip Ingham. The Autophagy Pathway component, Atg10, is required for skeletal and cardiac muscle fibre assembly in zebrafish. [Manuscript]

History

Defence date

2011-10-07

Department

  • Department of Microbiology, Tumor and Cell Biology

Publisher/Institution

Karolinska Institutet

Main supervisor

Ingham, Philip

Publication year

2011

Thesis type

  • Doctoral thesis

ISBN

978-91-7457-429-6

Number of supporting papers

3

Language

  • eng

Original publication date

2011-08-15

Author name in thesis

Lee, Samantha Lin Chiou

Original department name

Department of Microbiology, Tumor and Cell Biology

Place of publication

Stockholm

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