{"id":22,"date":"2020-04-23T17:13:39","date_gmt":"2020-04-23T17:13:39","guid":{"rendered":"https:\/\/lab.research.sickkids.ca\/taylor\/?page_id=22"},"modified":"2020-09-24T16:28:06","modified_gmt":"2020-09-24T16:28:06","slug":"medulloblastoma","status":"publish","type":"page","link":"https:\/\/lab.research.sickkids.ca\/taylor\/medulloblastoma\/","title":{"rendered":"Medulloblastoma"},"content":{"rendered":"

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Medulloblastoma<\/span><\/b>\u00a0<\/span><\/h1>\n

Our Medulloblastoma (MB) projects are driven by the tumour and sequencing data that form part of the Medulloblastoma Advanced Genomics International Consortium (MAGIC). MAGIC is a SickKids-based consortium of clinicians, scientists, and pathologists from over <\/span>85<\/span> cities around the world who have collectively contributed frozen medulloblastoma samples to the genomics efforts in Toronto.\u00a0<\/span>[\/vc_column_text][\/vc_column][\/vc_row][vc_row][vc_column width=”1\/2″][vc_column_text]<\/p>\n

Medulloblastoma is a not a single disease<\/h3>\n

Medulloblastoma is an embryonal tumour of the cerebellum that was thought to represent a single disease entity. <\/span>Data from the<\/span> Taylor Lab <\/span>and others, and accepted in an international consensus statement, Taylor et. al 2011 have agreed that MB is in fact comprised of four molecularly distinct diseases that have their own epidemiology, demographics, clinical presentation, transcriptional profile, somatic genetic events, and clinical outcomes:<\/span><\/p>\n

    \n
  1. Wnt<\/span> (due to hyperactivity of <\/span>Wnt<\/span> signaling)<\/span><\/li>\n
  2. Shh<\/span> (due to hyperactivity of <\/span>Shh<\/span> signaling)<\/span><\/li>\n
  3. Group 3<\/span><\/li>\n
  4. Group 4<\/span><\/li>\n<\/ol>\n

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    Medulloblastoma is extremely heterogenic<\/h3>\n

    More recently we have<\/span> demonstrated that medulloblastoma is <\/span>even more heterogenic than thought and may in fact be up to 12 different diseases<\/span> (<\/span>Cancer Cell, 2017; Nature, 2017) and that there is clinically significant heterogeneity in metastatic medulloblastomas (Nature, 2012, 2016; Nature Genetics, 2017). <\/span>We have also shown that these<\/span> cerebellar tumours are a disorder of early brain development, a finding which provides a proximate explanation for the peak incidence of cerebellar tumours in early childhood (Nature, 2019).<\/span>\u00a0<\/span>[\/vc_column_text][\/vc_column][\/vc_row][vc_row][vc_column][vc_row_inner][vc_column_inner width=”2\/3″][vc_column_text]<\/p>\n

    Current medulloblastoma research<\/h3>\n

    O<\/span>ur current research is focused on metastases<\/span> b<\/span>ecause t<\/span>he <\/span>main <\/span>cause of death from MB is not the primary tumour, but rather the metastases that arise from the primary tumour<\/span>. Unfortunately, MB metastases are biologically very different from their primary tumour, which means the same therapy cannot be applied to both. <\/span>Despite the urgent need for treatment innovation, there are currently no drugs <\/span>approved or in clinical trials for the treatment of this disease, nor are there any promising candidates.<\/span> D<\/span>ata from our lab shows that MB can metastasize through the blood syste<\/span>m, and that manipulation of trafficking systems <\/span>can drive\/attenuate metastatic phenotypes. <\/span>We are now<\/span> validating <\/span>these systems as targets;<\/span> we believe this will lead to rapidly translatable results and the development of clinical trial<\/span>s<\/span> that would accrue patients from this underserved and highly burdened population.<\/span>[\/vc_column_text][\/vc_column_inner][vc_column_inner width=”1\/3″][vc_single_image image=”487″ img_size=”medium” add_caption=”yes” alignment=”center” style=”vc_box_shadow_3d” onclick=”link_image” css_animation=”fadeIn”][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row][vc_column width=”1\/2″ offset=”vc_hidden-sm vc_hidden-xs”]