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Neoadjuvant radiotherapy for rectal cancer management

World Journal of Gastroenterology 2019年第33期25卷 4850-4869页

作者： Gerard Feeney Rishabh Sehgal Margaret Sheehan Aisling Hogan mark regan Myles Joyce Michael Kerin Department of General/Colorectal Surgery Galway University HospitalGalway H91 YR71Ireland Department of Histopathology Galway University HospitalGalway H91 YR71Ireland

Thirty per cent of all colorectal tumours develop in the *** location of the rectum within the bony pelvis and its proximity to vital structures presents significant therapeutic challenges when considering neoadjuvant options and surgical *** patients with early rectal cancer can be adequately managed by surgery ***,a significant proportion of patients with rectal cancer present with locally advanced disease and will potentially benefit from down staging prior to *** therapy involves a variety of options including radiotherapy,chemotherapy used alone or in *** radiotherapy in rectal cancer has been shown to be effective in reducing tumour burden in advance of curative *** gold standard surgical rectal cancer management aims to achieve surgical removal of the tumour and all draining lymph nodes,within an intact mesorectal package,in order to minimise local *** is critically important that all rectal cancer cases are discussed at a multidisciplinary meeting represented by all relevant ***-operative staging including CT thorax,abdomen,pelvis to assess for distal disease and magnetic resonance imaging to assess local involvement is *** radiology and MDT discussion are integral in identifying patients who require neoadjuvant *** Neoadjuvant radiotherapy is potentially beneficial it may also result in morbidity and thus should be reserved for those patients who are at a high risk of local failure,which includes patients with nodal involvement,extramural venous invasion and threatened circumferential *** aim of this review is to discuss the role of neoadjuvant radiotherapy in the management of rectal cancer.

关键词： Rectal cancer Neoadjuvant therapy Low anterior resection syndrome Stoma Transanal endoscopic microsurgery Trans-anal total mesorectal excision Robotic surgery Watch and wait

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Assembly of a parts list ofthe human mitotic cell cycle machinery

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Journal of Molecular Cell Biology 2019年第8期11卷 703-718页

作者： Bruno Giott Sz-Hau Chen mark W.Barnett Tim regan Tony Ly Stefan Wiemann David A.Hume Tom C.Freeman The Roslin Institute University of Edinburgh Easter Bush Midlothian EH25 9RG Scotland UK Biosciences and Biotechnology Institute EDyP Department CEA Grenoble 17 rue des Martyrs 38054 Grenoble France Wellcome Centre for Cell Biology University of Edinburgh Swann Building Edinburgh EH9 3BF Scotland UK Molecular Genome Analysis (B050) Deutsches Krebsforschungszentrum Im Neuenheimer Feld 580 69120 Heidelberg Germany Mater Research Institute University of Queensland Level 3 Aubigny Place Raymond Terrace South Brisbane Qld 4101 Australia

The set of proteins required for mitotic division remains poorly characterized. Here, an extensive series of correlation analyses of human and mouse transcriptomics data were performed to identify genes strongly and reproducibly associated with cells undergoing S/G2-M phases of the cell cycle. In so doing, 701 cell cycle-associated genes were defined and while it was shown that many are only expressed during these phases, the expression of others is also driven by alternative promoters. Of this list, 496 genes have known cell cycle functions, whereas 205 were assigned as putative cell cycle genes, 53 of which are functionally uncharacterized. Among these, 27 were screened for subcellular localization revealing many to be nuclear localized and at least three to be novel centrosomal proteins. Furthermore, 10 others inhibited cell proliferation upon siRNA knockdown. This study presents the first comprehensive list of human cell cycle proteins, identifying many new candidate proteins.

关键词： cell cycle systems biology gene expression transcriptome network analysis

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