P
Paul Crea
Researcher at St. Vincent's Health System
Publications - 12
Citations - 825
Paul Crea is an academic researcher from St. Vincent's Health System. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 8, co-authored 12 publications receiving 752 citations. Previous affiliations of Paul Crea include Garvan Institute of Medical Research.
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Journal ArticleDOI
PI3K pathway activation in breast cancer is associated with the basal‐like phenotype and cancer‐specific mortality
Elena Lopez-Knowles,Sandra A O'Toole,Catriona M. McNeil,Catriona M. McNeil,Ewan K.A. Millar,Min Ru Qiu,Min Ru Qiu,Paul Crea,Roger J. Daly,Roger J. Daly,Elizabeth A. Musgrove,Elizabeth A. Musgrove,Robert L. Sutherland,Robert L. Sutherland +13 more
TL;DR: It is concluded that >70% of breast cancers have an alteration in at least 1 component of the PI3K pathway and this might be exploited to therapeutic advantage especially in “basal‐like” cancers.
Journal ArticleDOI
The key hypoxia regulated gene CAIX is upregulated in basal-like breast tumours and is associated with resistance to chemotherapy.
E Y Tan,M Yan,M Yan,Leticia Campo,Cheng Han,E Takano,E Takano,Helen Turley,I Candiloro,I Candiloro,Francesco Pezzella,K C Gatter,Ewan K.A. Millar,Ewan K.A. Millar,Sandra A O'Toole,Sandra A O'Toole,Catriona M. McNeil,Catriona M. McNeil,Paul Crea,Davendra Segara,Robert L. Sutherland,Adrian L. Harris,Stephen B. Fox,Stephen B. Fox +23 more
TL;DR: The association between basal phenotype and CAIX suggests that the more aggressive behaviour of these tumours is partly due to an enhanced hypoxic response and raises the possibility that targeted therapy against HIF pathway or downstream genes such as CAs may be an approach to investigate for these patients.
Journal ArticleDOI
Cytoplasmic Localization of β-Catenin is a Marker of Poor Outcome in Breast Cancer Patients
Elena Lopez-Knowles,Sarah J. Zardawi,Catriona M. McNeil,Ewan K.A. Millar,Paul Crea,Elizabeth A. Musgrove,Robert L. Sutherland,Sandra A O'Toole +7 more
TL;DR: An immunohistochemical study measuring the levels and subcellular localization of β-catenin in 292 invasive ductal breast cancers with known treatment and outcome found a low β- catenin MTC score is associated with an adverse outcome in breast cancer, which may be of mechanistic significance in the disease process.
Journal ArticleDOI
c-Myc overexpression and endocrine resistance in breast cancer.
Catriona M. McNeil,C. Marcelo Sergio,Luke R. Anderson,Claire K. Inman,Sarah A. Eggleton,Niamh C Murphy,Niamh C Murphy,Ewan K.A. Millar,Ewan K.A. Millar,Paul Crea,Paul Crea,James G. Kench,James G. Kench,James G. Kench,M. Chehani Alles,Margaret Gardiner-Garden,Christopher J. Ormandy,Christopher J. Ormandy,Alison J. Butt,Alison J. Butt,Susan Henshall,Susan Henshall,Elizabeth A. Musgrove,Elizabeth A. Musgrove,Robert L. Sutherland,Robert L. Sutherland +25 more
TL;DR: It is confirmed that c-Myc overexpression is a common event in breast cancer, and that this is associated with resistance to antiestrogens in vitro, and the development of an experimental paradigm for the discovery and validation of genes involved in estrogen signalling, and c- myc-mediated-antiestrogen resistance.
Journal ArticleDOI
High Notch1 protein expression is an early event in breast cancer development and is associated with the HER-2 molecular subtype.
Sarah J. Zardawi,Ibrahim M. Zardawi,Catriona M. McNeil,Catriona M. McNeil,Ewan K.A. Millar,Ewan K.A. Millar,Duncan J. Mcleod,Adrienne Morey,Paul Crea,Niamh C Murphy,Mark Pinese,Elena Lopez-Knowles,Samantha R. Oakes,Christopher J. Ormandy,Min Ru Qiu,Anne Hamilton,Andrew J. Spillane,Andrew J. Spillane,Cheok Soon Lee,Cheok Soon Lee,Robert L. Sutherland,Robert L. Sutherland,Elizabeth A. Musgrove,Elizabeth A. Musgrove,Sandra A O'Toole,Sandra A O'Toole,Sandra A O'Toole +26 more
TL;DR: Zardawi S J, Zardawi I, McNeil C M, Millar E K A, McLeod D, Morey A L, Crea P, Murphy N C, Pinese M, Lopez‐Knowles E, Oakes S R, Ormandy C J, Qiu M R, Hamilton A, Spillane A, Soon Lee C, Sutherland R L, Musgrove E A & O’Toole S A .