Publications by authors named "B A Gusterson"

Background: Protein markers of cellular proliferation, hypoxia, apoptosis, cell cycle checkpoints, growth factor signalling and inflammation in localised prostate tumours have previously shown prognostic ability. A translational substudy within the CHHiP trial of radiotherapy fractionation evaluated whether these could improve prediction of prognosis and assist treatment stratification following either conventional or hypofractionated radiotherapy.

Methods: Using case:control methodology, patients with biochemical or clinical failure after radiotherapy (BCR) were matched to patients without recurrence according to established prognostic factors (Gleason score, presenting PSA, tumour-stage) and fractionation schedule.

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Breast cancer heterogeneity has made it challenging to identify mechanisms critical to the initial stages of their genesis in vivo. Here, we sought to interrogate the role of YB-1 in newly arising human breast cancers as well as in established cell lines. In a first series of experiments, we found that short-hairpin RNA-mediated knockdown of YB-1 in MDA-MB-231 cells blocked both their local tumour-forming and lung-colonising activity in immunodeficient mice.

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Article Synopsis
  • Evidence shows that tumour infiltrating lymphocytes (TILs) play a crucial role in breast cancer, but their variability in ductal carcinoma in situ (DCIS) and its impact on cancer progression is not fully understood.
  • A new deep learning tool called UNMaSk was created to analyze the spatial arrangement of DCIS tissue and TILs, using automated detection methods for clarity.
  • Findings revealed that pure DCIS had higher overall TIL counts than adjacent DCIS, but TILs were less likely to cluster around pure DCIS ducts, suggesting a different inflammation pattern in adjacent cases that might influence cancer development.
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Human breast cancers referred to as "basal-like" are of interest because they lack effective therapies and their biology is poorly understood. The term basal-like derives from studies demonstrating tumor gene expression profiles that include some transcripts characteristic of the basal cells of the normal adult human mammary gland and others associated with a subset of normal luminal cells. Elucidating the mechanisms responsible for the profiles of basal-like tumors is an active area of investigation.

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