Literature DB >> 19495563

Anaplastic oligoastrocytoma in Turcot syndrome.

Joachim Baehring1,2, Pei Hui3, Joseph Piepmeier4, Serguei I Bannykh5.   

Abstract

Turcot syndrome (TS), a rare variant of hereditary non-polyposis colorectal cancer (HNPCC), is characterized by familial clustering of cancer of the large bowel, extracolonic body sites and brain. It is caused by germline mutations in genes encoding for components of the DNA mismatch repair system. We report a 72 year old woman with anaplastic oligoastrocytoma in the setting of TS. Careful analysis of tumor DNA is required to exclude the chance occurrence of a brain tumor in HNPCC kindreds and increase our understanding of the pathogenesis of the disease. Our case adds to the handful of cases published with detailed molecular data previously.

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Year:  2009        PMID: 19495563     DOI: 10.1007/s11060-009-9928-y

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  25 in total

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Journal:  Genes Chromosomes Cancer       Date:  1999-06       Impact factor: 5.006

2.  Detection of microsatellite instability by fluorescence multiplex polymerase chain reaction.

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Journal:  J Mol Diagn       Date:  2000-02       Impact factor: 5.568

3.  Frameshift mutator mutations.

Authors:  S Malkhosyan; N Rampino; H Yamamoto; M Perucho
Journal:  Nature       Date:  1996-08-08       Impact factor: 49.962

4.  Microsatellite instability in the insulin-like growth factor II receptor gene in gastrointestinal tumours.

Authors:  R F Souza; R Appel; J Yin; S Wang; K N Smolinski; J M Abraham; T T Zou; Y Q Shi; J Lei; J Cottrell; K Cymes; K Biden; L Simms; B Leggett; P M Lynch; M Frazier; S M Powell; N Harpaz; H Sugimura; J Young; S J Meltzer
Journal:  Nat Genet       Date:  1996-11       Impact factor: 38.330

5.  Somatic frameshift mutations in the BAX gene in colon cancers of the microsatellite mutator phenotype.

Authors:  N Rampino; H Yamamoto; Y Ionov; Y Li; H Sawai; J C Reed; M Perucho
Journal:  Science       Date:  1997-02-14       Impact factor: 47.728

Review 6.  Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review.

Authors:  H T Lynch; T C Smyrk; P Watson; S J Lanspa; J F Lynch; P M Lynch; R J Cavalieri; C R Boland
Journal:  Gastroenterology       Date:  1993-05       Impact factor: 22.682

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Authors:  Asad Umar; C Richard Boland; Jonathan P Terdiman; Sapna Syngal; Albert de la Chapelle; Josef Rüschoff; Richard Fishel; Noralane M Lindor; Lawrence J Burgart; Richard Hamelin; Stanley R Hamilton; Robert A Hiatt; Jeremy Jass; Annika Lindblom; Henry T Lynch; Païvi Peltomaki; Scott D Ramsey; Miguel A Rodriguez-Bigas; Hans F A Vasen; Ernest T Hawk; J Carl Barrett; Andrew N Freedman; Sudhir Srivastava
Journal:  J Natl Cancer Inst       Date:  2004-02-18       Impact factor: 13.506

8.  Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations.

Authors:  R D Kolodner; N R Hall; J Lipford; M F Kane; M R Rao; P Morrison; L Wirth; P J Finan; J Burn; P Chapman
Journal:  Genomics       Date:  1994-12       Impact factor: 5.736

9.  The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer.

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Journal:  Cell       Date:  1993-12-03       Impact factor: 41.582

10.  Mutations of two PMS homologues in hereditary nonpolyposis colon cancer.

Authors:  N C Nicolaides; N Papadopoulos; B Liu; Y F Wei; K C Carter; S M Ruben; C A Rosen; W A Haseltine; R D Fleischmann; C M Fraser
Journal:  Nature       Date:  1994-09-01       Impact factor: 49.962

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  1 in total

Review 1.  Constitutional mismatch repair-deficiency: current problems and emerging therapeutic strategies.

Authors:  Malak Abedalthagafi
Journal:  Oncotarget       Date:  2018-10-23
  1 in total

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