Investigator

Simon Chu

MONASH UNIVERSITY

SCSimon Chu
Papers(1)
Enhanced Expression o…
Collaborators(4)
Ashfaqul HoqueFadi CharcharJason KellyRodney Luwor
Institutions(5)
Hudson Institute Of M…Saint Vincent's Insti…Federation UniversityFiona Elsey Cancer Re…The Royal Melbourne H…

Papers

Enhanced Expression of Mitochondrial Magmas Protein in Ovarian Carcinomas: Magmas Inhibition Facilitates Antitumour Effects, Signifying a Novel Approach for Ovarian Cancer Treatment

Mitochondrial-associated granulocyte macrophage colony-stimulating factor (Magmas) is a unique protein located in the inner membrane of mitochondria, with an active role in scavenging reactive oxygen species (ROS) in cellular systems. Ovarian cancer (OC), one of the deadliest gynaecological cancers, is characterised by genomic instability, affected by ROS production in the tumour microenvironment. This manuscript discusses the role of Magmas and efficacy of its novel small molecule inhibitor BT#9 in OC progression, metastasis, and chemoresistance. Magmas expression levels were significantly elevated in high-grade human OC compared to benign tumours by immunohistochemistry. The inhibition of Magmas by BT#9 enhanced ROS production and reduced mitochondrial membrane permeability, basal respiration, mitochondrial ATP production, and cellular functions, such as the proliferation and migration of OC cell lines in vitro. Oral administration of BT#9 in vivo significantly reduced tumour growth and spread and enhanced the survival of mice without having any effect on the peritoneal organs. These data suggest that Magmas is functionally important for OC growth and spread by affecting ROS levels and that the inhibition of Magmas activity by BT#9 may provide novel clinical benefits for patients with this malignancy.

70Works
1Papers
4Collaborators
Ovarian NeoplasmsCell Line, TumorGranulosa Cell TumorApoptosisNecrosisDrug Resistance, NeoplasmX-Linked Inhibitor of Apoptosis ProteinNeoplasm Staging

Positions

Researcher

MONASH UNIVERSITY

2009–

Senior Research Officer / L'Oreal Paris Research Fellow

Hudson Institute of Medical Research · Steroid Receptor Biology

2007–

Post Doc

Institut Pasteur du Cambodge · Molecular Virology

2005–

Post Doc

Prince Henry's Institute of Medical Research · Steroid Receptor Biology

1997–

Research Assistant

Prince Henry's Institue of Medical Research · Steroid Receptor Biology

Country

AU

Keywords
ovarian cancergranulosa cell tumorFOXL2estrogen receptor beta