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Chromosomal instability in adult-type diffuse gliomas.
Richardson, Timothy E; Walker, Jamie M; Abdullah, Kalil G; McBrayer, Samuel K; Viapiano, Mariano S; Mussa, Zarmeen M; Tsankova, Nadejda M; Snuderl, Matija; Hatanpaa, Kimmo J.
Affiliation
  • Richardson TE; Department of Pathology, Molecular, and Cell-Based Medicine, Icahn School of Medicine at Mount Sinai, Annenberg Building, 15th Floor, 1468 Madison Avenue, New York, NY, 10029, USA. timothy.richardson@mountsinai.org.
  • Walker JM; Department of Pathology, Molecular, and Cell-Based Medicine, Icahn School of Medicine at Mount Sinai, Annenberg Building, 15th Floor, 1468 Madison Avenue, New York, NY, 10029, USA.
  • Abdullah KG; Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • McBrayer SK; Department of Neurosurgery, University of Pittsburgh School of Medicine, 200 Lothrop St, Pittsburgh, PA, 15213, USA.
  • Viapiano MS; Hillman Comprehensive Cancer Center, University of Pittsburgh Medical Center, 5115 Centre Ave, Pittsburgh, PA, 15232, USA.
  • Mussa ZM; Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
  • Tsankova NM; Children's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
  • Snuderl M; Department of Neuroscience and Physiology, State University of New York, Upstate Medical University, Syracuse, NY, 13210, USA.
  • Hatanpaa KJ; Department of Neurosurgery, State University of New York, Upstate Medical University, Syracuse, NY, 13210, USA.
Acta Neuropathol Commun ; 10(1): 115, 2022 08 17.
Article in En | MEDLINE | ID: mdl-35978439
Chromosomal instability (CIN) is a fundamental property of cancer and a key underlying mechanism of tumorigenesis and malignant progression, and has been documented in a wide variety of cancers, including colorectal carcinoma with mutations in genes such as APC. Recent reports have demonstrated that CIN, driven in part by mutations in genes maintaining overall genomic stability, is found in subsets of adult-type diffusely infiltrating gliomas of all histologic and molecular grades, with resulting elevated overall copy number burden, chromothripsis, and poor clinical outcome. Still, relatively few studies have examined the effect of this process, due in part to the difficulty of routinely measuring CIN clinically. Herein, we review the underlying mechanisms of CIN, the relationship between chromosomal instability and malignancy, the prognostic significance and treatment potential in various cancers, systemic disease, and more specifically, in diffusely infiltrating glioma subtypes. While still in the early stages of discovery compared to other solid tumor types in which CIN is a known driver of malignancy, the presence of CIN as an early factor in gliomas may in part explain the ability of these tumors to develop resistance to standard therapy, while also providing a potential molecular target for future therapies.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromothripsis / Glioma Type of study: Prognostic_studies Limits: Adult / Humans Language: En Journal: Acta Neuropathol Commun Year: 2022 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromothripsis / Glioma Type of study: Prognostic_studies Limits: Adult / Humans Language: En Journal: Acta Neuropathol Commun Year: 2022 Document type: Article Affiliation country: United States Country of publication: United kingdom