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DTSTART:19960101T000000 END:STANDARD BEGIN:STANDARD TZNAME:GMT TZOFFSETFROM:+0100 TZOFFSETTO:+0000 DTSTART:19961027T020000 RRULE:FREQ=YEARLY;BYMONTH=10;BYDAY=-1SU END:STANDARD END:VTIMEZONE BEGIN:VEVENT DTSTAMP:20260513T015231Z DTSTART;VALUE=DATE-TIME:20200205T130000 DTEND;VALUE=DATE-TIME:20200205T140000 SUMMARY:BMS Divisional Seminar by Professor Lawrence Young\, Dr Samuel De an\, Division of Biomedical Sciences\, ÌÇÐÄTV Medical School\, Universi ty of ÌÇÐÄTV TZID:Europe/London UID:20200205-8a17841b6f85aa19016fa3b46f625dee@warwick.ac.uk CREATED:20200131T100849Z DESCRIPTION:Professor Lawrence Young Dissecting the role of the tumour mi croenvironment in EBV-associated nasopharyngeal carcinoma Abstract: The cancer mass represents a dynamic landscape where a heterogenous populati on of tumour cells interact with a variety of infiltrating host cells\, extracellular matrix proteins and secreted factors. This tumour microenv ironment (TME) influences the development\, growth and spread of cancer while also shaping therapeutic responses. Nasopharyngeal carcinoma (NPC) is an undifferentiated tumour with an extensive but ill-defined TME com prising infiltrating T cells\, NK cells\, macrophages and fibroblasts. T he precise role of the TME on the growth and invasiveness of NPC is unkn own but it is likely that these infiltrating cells provide an essential support to the growth and survival of the tumour cells. The unique geogr aphic distribution of NPC in China and South-East Asia\, along with the presence of latent Epstein-Barr virus (EBV) infection in every tumour ce ll\, provide insights into the aetiology of this particular malignancy. The TME may support the maintenance of stable EBV infection in carcinoma cells and create an immune suppressive milieu that facilitates immune e vasion. Better definition of the TME in NPC and its relationship to EBV infection will improve our understanding of NPC pathogenesis and support the development of novel therapeutic and preventative interventions. Dr Samuel Dean Flagellum composition and function in protozoan parasites A bstract - Trypanosomatids are microscopic vector-borne parasites that ca use wide-spread human and animal diseases. They currently infect ~17 mil lion people\, kill 80\,000 people annually and are a terrible agricultur al and economic burden upon developing counties. There is an urgent need for new therapies because no vaccines are available and existing drugs are often ineffective and toxic. Central to their ability to spread and cause disease is a protrusion of the surface called the flagellum. The f lagellum is essential for parasite movement and host-parasite interactio n\, and flagellum function is required for parasite virulence and transm ission. Flagella have three distinct domains defined by the arrangement of their microtubules: the basal body that is embedded in the cytoplasm\ , the axoneme that protrudes from the cell body\, and the transition zon e (TZ) that links the two. The axonemes of most motile flagella contain a central pair (CP) of microtubules that extend from the TZ and are esse ntial for flagellum beating\; defects in the CP cause the human patholog ies hydrocephalus and primary ciliary dyskinesia. Further\, in recent ye ars the TZ has emerged as central to flagellum function and it is the lo cation of many of the proteins and complexes that are implicated in a cl ass of human genetic diseases called ‘ciliopathies’. My research has use d a novel proteomics method specifically designed to isolate insoluble c ytoskeletal structures for proteomics analysis. Using this methodology\, I determined the composition of the trypanosome TZ and discovered that two of its proteins act as CP nucleating factors. My lab will focus on a ddressing the following questions: 1) How do trypanosome TZ proteins nuc leate the CP microtubules? 2) What is the role of the TZ in other flagel lum functions? 3) What is the role of the metazoan orthologs of trypanos ome TZ proteins in ciliary function and human disease? LOCATION:GLT2\, ÌÇÐÄTV Medical School CATEGORIES:BiomedicalSciences,DivisionalSeminars LAST-MODIFIED:20200131T100849Z ORGANIZER;CN=Jas Bains: END:VEVENT END:VCALENDAR