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Adrian P. Wiegmans

Researcher at QIMR Berghofer Medical Research Institute

Publications -  17
Citations -  1721

Adrian P. Wiegmans is an academic researcher from QIMR Berghofer Medical Research Institute. The author has contributed to research in topics: DNA repair & Cancer. The author has an hindex of 11, co-authored 16 publications receiving 1273 citations.

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Optimized exosome isolation protocol for cell culture supernatant and human plasma

TL;DR: It is shown that concentration of cell culture conditioned media using ultrafiltration devices results in increased vesicle isolation when compared to traditional ultracentrifugation protocols, and it is demonstrated that size exclusion isolation is comparable to density gradient purification of exosomes.
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Harnessing the complexity of DNA-damage response pathways to improve cancer treatment outcomes

TL;DR: It is proposed that promising combinations of DNA-damaging anticancer treatments with DDR-pathway inhibition would be further enhanced by activating downstream apoptotic pathways, ensuring that actual cell death is the preferred outcome of cancer treatment instead of other responses, including reversible cell cycle arrest, autophagy or senescence.
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Targeting homologous recombination, new pre-clinical and clinical therapeutic combinations inhibiting RAD51.

TL;DR: The potential treatment efficacy and future clinical applications of RAD51 inhibitors as single agents and in combination with other therapies are scrutinized and the best therapeutic options are considered.
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Rad51 supports triple negative breast cancer metastasis.

TL;DR: Analysis of immunohistochemistry in an independent cohort of 235 were sporadic breast tumours suggested that RAD51 expression is increased during breast cancer progression and metastasis and an oncogenic role for RAD51 when deregulated and subsequent knockdown repressed cancer cell migration in vitro and reduced primary tumor growth in a syngeneic mouse model in vivo.
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Kinome profiling reveals breast cancer heterogeneity and identifies targeted therapeutic opportunities for triple negative breast cancer

TL;DR: The combination of Erk5 and Hsp90 inhibitors was effective in vitro and in vivo against TNBC leading to upregulation of pro-apoptotic effectors, contributing to proteomic profiling and improving understanding of TNBC heterogeneity to provide therapeutic opportunities for this disease.