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2007 Winter Meeting - London - The Pathological Society of Great ...

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S5HOW TO BE A GOOD TEACHER{P} P DomizioPr<strong>of</strong>essor <strong>of</strong> Pathology Education, Barts and the <strong>London</strong>, Queen Mary’sSchool <strong>of</strong> Medicine, <strong>London</strong>, United KingdomGood teachers are role models as well as educators and there is no doubt thatthey can inspire their students to go along certain career paths. <strong>The</strong>re has beenmuch debate in the educational literature about what makes a good teacher, buta widely accepted definition is still lacking. Most students describe a goodteacher as accessible, enthusiastic, passionate, humorous, caring and nonjudgmental.Good teachers are learner-orientated – they take into account howmuch their students already know, they put learning into context and theyactively engage their students in the learning process. Good teachers provide asupportive, trusting and non-threatening environment in which the studentpositively enjoys learning. Giving a good lecture is an art, akin to a stageperformance in which the lecturer is protagonist and holds the audience’sattention to the end. Some <strong>of</strong> the skills involved in giving a good lecture stemfrom the lecturer’s personality, but others can be practiced and learnt. Goodlectures are well-planned, well-structured, well-delivered and properly timed.<strong>The</strong> personal rewards for being considered a good teacher are high. Atpr<strong>of</strong>essional level, the climate is slowly changing with increasing recognitionand promotion <strong>of</strong> good teachers.S6How to Write a Scientific Paper and Get it Published{P} CS HerringtonUniversity <strong>of</strong> St Andrews, Fife, United Kingdom<strong>The</strong>re are numerous issues that influence whether a paper gets published, butmany <strong>of</strong> these relate to the central underlying principle that it should address aspecific hypothesis, and do so in a concise, informative way. <strong>The</strong> firstimpressions <strong>of</strong> editors and reviewers are key to the success <strong>of</strong> a submission andare <strong>of</strong>ten determined by the title, abstract and figures: these components aretherefore worthy <strong>of</strong> particular attention. <strong>The</strong>re is an increasing trend for authorsto ‘aim high’ (by which they usually mean submission to journals with a highimpact factor) and the probability <strong>of</strong> success with the major internationaljournals is increased significantly if the basic principles above are adhered to,and attention is paid to the instructions for authors for that particular journal.<strong>The</strong>re are, however, no guarantees and failure to persuade one journal topublish your work should not deter you from trying others.S7Proteomics and Prostate Carcinoma{P} L EgevadInternational Agency for Research on Cancer (IARC), Lyon, FranceAs a result <strong>of</strong> earlier detection <strong>of</strong> prostate cancer, a majority <strong>of</strong> patients nowhave non-palpable tumors (T1c) <strong>of</strong> low grade (Gleason score 6). Consequently,some <strong>of</strong> the prognostic discrimination obtained by staging and grading is lostand there is a need for adjunctive prognostic indicators. In the search for suchtumor markers an exploration <strong>of</strong> the human proteome may be fruitful.Two-dimensional gel electrophoresis (2-DE) is presently the most powerfulmethod for analysis <strong>of</strong> cellular protein phenotype. Proteins are separatedaccording to their size and charge, gels are compared by image analysis, proteinspots <strong>of</strong> interest are excised and proteins identified by mass spectrometry. Onprostate samples, 2-DE has been used for mapping <strong>of</strong> differential proteinexpression <strong>of</strong> the anatomical zones, benign tissue vs. prostate cancer andcorrelations with tumor grade. Disadvantages with 2-DE are that the techniqueis time-consuming, expensive and requires large tissue samples.Non 2-DE methods, such as SELDI, ICAT and array based technologies,generally require smaller sample sizes and are more automated than 2-DE.However, with some <strong>of</strong> these methods only a limited set <strong>of</strong> proteins are detectedin each assay and concerns have been raised about protein identification anddata validation.S8<strong>The</strong> Value <strong>of</strong> Tissue Microarrays in Urological Pathology.{P} DM BerneyBarts and <strong>The</strong> <strong>London</strong>, Queen Mary School <strong>of</strong> Medicine and Dentistry,<strong>London</strong>, UK, United KingdomTissue microarrays are a technique for high throughput analysis <strong>of</strong> tissues.Urological pathology <strong>of</strong>fers many opportunities for TMA construction <strong>of</strong> largeseries for biomarker analysis. Prerequisites for analysis are the identification <strong>of</strong>areas suitable for array and sampling multiple areas to allow for heterogeneity.Uses <strong>of</strong> TMA include the retrospective investigation <strong>of</strong> prognostic markers andthe potential <strong>of</strong> prospectively correlating markers with chemo andradiosensitivity to allow individualised tumour therapy in the future.This review will outline uropathological project undertaken in <strong>The</strong> OrchidTissue laboratory in a range <strong>of</strong> malignancies including germ cell neoplasms,renal tumours, squamous cell carcinoma <strong>of</strong> the penis and prostate cancer.Technical problems will be discussed.<strong>The</strong> Trans-Atlantic Prostate Group has produced an array <strong>of</strong> over 900 prostatecancer patients who had TURPs between 1991 and 1996, and treated bywatchful waiting. TMA has allowed a vast number <strong>of</strong> potential biomarkers tobe investigated. Recent advances in technology have allowed biopsy material tobe arrayed successfully. This vastly increases the power <strong>of</strong> TMAs in urologicalpathology, particularly in the prostate where retrospective biopsy series can beanalysed.Immunochemistry is not the only technique that can be used successfully inTMAs. Fluorescence ISH has shown specific chromosomal translocations inprostate TMAs, and chromogenic ISH can better correlate abnormalities withlight microscopic appearances.<strong>Winter</strong> <strong>Meeting</strong> (191 st ) 3–5 January <strong>2007</strong> Scientific Programme59

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