Anti-mitotic therapies in cancer
Tischer and Gergely review the cell biology behind microtubule poisons and their clinical use in cancer patients.
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Published in | The Journal of cell biology Vol. 218; no. 1; pp. 10 - 11 |
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Main Authors | , |
Format | Journal Article |
Language | English |
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United States
Rockefeller University Press
07.01.2019
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Abstract | Tischer and Gergely review the cell biology behind microtubule poisons and their clinical use in cancer patients. |
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AbstractList | Tischer and Gergely review the cell biology behind microtubule poisons and their clinical use in cancer patients. Tischer and Gergely discuss the anti-mitotic therapies in cancer. Chronic cellular proliferation is a hallmark of cancer, and therefore therapies targeting key pathways that drive and execute cell division have been a major research goal. The somatic cell division cycle culminates in mitosis, when the microtubule (MT)-based mitotic spindle captures, aligns, and then equally distributes chromosomes into daughter cells. Polo-like kinase 1 (PLK1) and Aurora kinases (AurA and AurB) play pleiotropic roles during mitosis; they are important for mitotic entry and exit, spindle assembly, and also the capture, alignment, and segregation of chromosomes. |
Author | Tischer, Julia Gergely, Fanni |
AuthorAffiliation | Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK |
AuthorAffiliation_xml | – name: Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK |
Author_xml | – sequence: 1 givenname: Julia surname: Tischer fullname: Tischer, Julia organization: Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK – sequence: 2 givenname: Fanni orcidid: 0000-0002-2441-8095 surname: Gergely fullname: Gergely, Fanni email: fanni.gergely@cruk.cam.ac.uk organization: Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK fanni.gergely@cruk.cam.ac.uk |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30545842$$D View this record in MEDLINE/PubMed |
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Copyright | Copyright Rockefeller University Press Jan 2019 2018 Tischer and Gergely 2018 |
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SubjectTerms | Antineoplastic Agents - therapeutic use Aurora Kinase A - antagonists & inhibitors Aurora Kinase A - genetics Aurora Kinase A - metabolism Aurora Kinase B - antagonists & inhibitors Aurora Kinase B - genetics Aurora Kinase B - metabolism Cancer Cancer therapies Cell Cycle Proteins - antagonists & inhibitors Cell Cycle Proteins - genetics Cell Cycle Proteins - metabolism Cell division Cell growth Cell Line, Tumor Chromosomes Clinical Trials as Topic Discussion Gene Expression Regulation, Neoplastic - drug effects Gene therapy Humans Kinases Kinesins - antagonists & inhibitors Kinesins - genetics Kinesins - metabolism Microtubules - drug effects Microtubules - metabolism Mitosis Mitosis - drug effects Neoplasms - drug therapy Neoplasms - genetics Neoplasms - metabolism Neoplasms - pathology Polo-like kinase Polo-Like Kinase 1 Protein Serine-Threonine Kinases - antagonists & inhibitors Protein Serine-Threonine Kinases - genetics Protein Serine-Threonine Kinases - metabolism Proto-Oncogene Proteins - antagonists & inhibitors Proto-Oncogene Proteins - genetics Proto-Oncogene Proteins - metabolism Signal Transduction Tubulin Modulators - therapeutic use |
Title | Anti-mitotic therapies in cancer |
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