Atypical Teratoid/Rhabdoid Tumors of the Central Nervous System

No abstract is available for this paper.

• Publication year

  2005

• Venue

  Journal of Neuro-Oncology

• Publication date

  2005-12-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/s11060-005-6762-8PMID 16195799
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• No evidence for epidermal growth factor receptor amplification and overexpression in atypical teratoid/rhabdoid tumors

  2006cited by this paper
• Non‐linkage of familial rhabdoid tumors to SMARCB1 implies a second locus for the rhabdoid tumor predisposition syndrome

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• Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: case study.

  2006cited by this paper
• Immunohistochemical Analysis of INI1 Protein in Malignant Pediatric CNS Tumors: Lack of INI1 in Atypical Teratoid/Rhabdoid Tumors and in a Fraction of Primitive Neuroectodermal Tumors without Rhabdoid Phenotype

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• Methylation of RASSF1A and TRAIL pathway-related genes is frequent in childhood intracranial ependymomas and benign choroid plexus papilloma.

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• Absence of expression of SMARCB1/INI1 in malignant rhabdoid tumors of the central nervous system, kidneys and soft tissue: an immunohistochemical study with implications for diagnosis

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• Targeting cyclin D1, a downstream effector of INI1/hSNF5, in rhabdoid tumors

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• Molecular genetics of atypical teratoid/rhabdoid tumors

  2006cited by this paper
• Predisposition to atypical teratoid/rhabdoid tumor due to an inherited INI1 mutation

  2006cited by this paper
• Primary malignant rhabdoid tumours of the central nervous system: An immunohistochemical and ultrastructural study

  2005cited by this paper
• SMARCB1/INI1 tumor suppressor gene is frequently inactivated in epithelioid sarcomas.

  2005cited by this paper
• Malignant Rhabdoid Tumor in a Pregnant Adult Female: Literature Review of Central Nervous System Rhabdoid Tumors

  2005cited by this paper
• Elevation of plasma and cerebrospinal fluid osteopontin levels in patients with atypical teratoid/rhabdoid tumor.

  2005cited by this paper
• Atypical teratoid rhabdoid tumors of childhood: diagnosis, treatment and challenges

  2005cited by this paper
• Chromosome 22q Deletions in Atypical Teratoid/Rhabdoid Tumors in Adults

  2005cited by this paper
• Cyclin D1 is overexpressed in atypical teratoid/rhabdoid tumor with hSNF5/INI1 gene inactivation

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• Rhabdoid tumours of the central nervous system

  2005cited by this paper
• Short communication Mutational analysis of hSNF5/INI1 and TP53 genes in choroid plexus carcinomas

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• INI1 expression is retained in composite rhabdoid tumors, including rhabdoid meningiomas

  2005cited by this paper
• Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood

  2005cited by this paper
• Loss of the hSNF5 gene concomitantly inactivates p21CIP/WAF1 and p16INK4a activity associated with replicative senescence in A204 rhabdoid tumor cells.

  2005cited by this paper
• Cancer-associated mutations in chromatin remodeler hSNF5 promote chromosomal instability by compromising the mitotic checkpoint.

  2005cited by this paper
• Clinicopathologic and cytogenetic analysis of malignant rhabdoid tumor of the central nervous system

  2005cited by this paper
• Pediatric embryonal tumor of the cerebellum with rhabdoid cells and novel intracytoplasmic inclusions: distinction from atypical teratoid/rhabdoid tumor

  2005cited by this paper
• Atypical teratoid/rhabdoid tumors (ATRT): improved survival in children 3 years of age and older with radiation therapy and high-dose alkylator-based chemotherapy.

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• Continuous remission of newly diagnosed and relapsed central nervous system atypical teratoid/rhabdoid tumor

  2005cited by this paper
• Primary malignant rhabdoid tumor of the central nervous system – a comprehensive review

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• Atypical teratoid/rhabdoid tumor case report: treatment with surgical excision, radiation therapy, and alternative medicines

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• Genetic ablation of Cyclin D1 abrogates genesis of rhabdoid tumors resulting from Ini1 loss.

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• INI1 Protein Expression Distinguishes Atypical Teratoid/Rhabdoid Tumor from Choroid Plexus Carcinoma

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• Increased expression of osteopontin gene in atypical teratoid/rhabdoid tumor of the central nervous system

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• Chromosome mechanisms and INI1 inactivation in human and mouse rhabdoid tumors.

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• Novel germ‐line deletion of SNF5/INI1/SMARCB1 gene in neonate presenting with congenital malignant rhabdoid tumor of kidney and brain primitive neuroectodermal tumor

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• Antitumor Activity of Gefitinib in Malignant Rhabdoid Tumor Cells In vitro and In vivo

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• Malignant rhabdoid tumor: primary intracranial manifestation in an adult

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• The Tumor Suppressor hSNF5/INI1 Modulates Cell Growth and Actin Cytoskeleton Organization

  2004cited by this paper
• Minireview: Cyclin D1: normal and abnormal functions.

  2004cited by this paper
• Central nervous system atypical teratoid/rhabdoid tumor: results of therapy in children enrolled in a registry.

  2004cited by this paper
• Primary Malignant Rhabdoid Tumors of the Central Nervous System: Considerations about Two Cases of Adulthood Presentation

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• Immunohistochemical Analysis of hSNF5/INI1 in Pediatric CNS Neoplasms

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• Double immunolabeling of central nervous system atypical teratoid/rhabdoid tumors

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• Loss of BRG1/BRM in human lung cancer cell lines and primary lung cancers: correlation with poor prognosis.

  2003cited by this paper
• INI1 expression induces cell cycle arrest and markers of senescence in malignant rhabdoid tumor cells

  2003cited by this paper
• A Unique Occurrence of a Cerebral Atypical Teratoid/Rhabdoid Tumor in an Infant and a Spinal Canal Primitive Neuroectodermal Tumor in her Father

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• TRAIL/Apo2L Ligands Induce Apoptosis in Malignant Rhabdoid Tumor Cell Lines

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• Atypical teratoid/rhabdoid tumors

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• Atypical teratoid/rhabdoid tumor of the central nervous system in children: an atypical series and review

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• Atypical Teratoid/Rhabdoid Tumors and Choroid Plexus Tumors: When Genetics “Surprise” Pathology

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• Alpha-internexin expression in medulloblastomas and atypical teratoid-rhabdoid tumors.

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• Cerebral Atypical Teratoid/Rhabdoid Tumor of Infancy: Long-Term Survival after Multimodal Treatment, also Including Triple Intrathecal Chemotherapy and Gamma Knife Radiosurgery--Case Report

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• Molecular analysis of the rhabdoid predisposition syndrome in a child: a novel germline hSNF5/INI1 mutation and absence of c-myc amplification

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• Comparative genomic hybridization and pathological findings in atypical teratoid/rhabdoid tumour of the central nervous system

  2003cited by this paper
• A key role of the hSNF5/INI1 tumour suppressor in the control of the G1-S transition of the cell cycle

  2002cited by this paper
• Aberrations of the hSNF5/INI1 gene are restricted to malignant rhabdoid tumors or atypical teratoid/rhabdoid tumors in pediatric solid tumors

  2002cited by this paper
• Alterations of the hSNF5/INI1 gene in central nervous system atypical teratoid/rhabdoid tumors and renal and extrarenal rhabdoid tumors.

  2002cited by this paper
• No evidence for hypermethylation of the hSNF5/INI1 promoter in pediatric rhabdoid tumors

  2002cited by this paper
• Re-expression of hSNF5/INI1/BAF47 in pediatric tumor cells leads to G1arrest associated with induction of p16ink4a and activation of RB

  2002cited by this paper
• The role of INI1 and the SWI/SNF complex in the development of rhabdoid tumors: meeting summary from the workshop on childhood atypical teratoid/rhabdoid tumors.

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• The WHO Classification of Tumors of the Nervous System

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• Choroid plexus tumours

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• Atypical Teratoid/Rhabdoid Tumors of the Central Nervous System: Clinical, Radiographic and Pathologic Features

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• Association between DNA content and tumor suppressor gene expression and aggressiveness of atypical teratoid/rhabdoid tumors

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• Atypical Teratoid/Rhabdoid Tumor of the Central Nervous System: Report on Workshop

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• Chromosomal imbalances in choroid plexus tumors.

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• Cell Cycle Arrest and Repression of Cyclin D1 Transcription by INI1/hSNF5

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• Mutation Analysis of Human Cytokeratin 8 Gene in Malignant Rhabdoid Tumor: A Possible Association with Intracytoplasmic Inclusion Body Formation

  2002cited by this paper
• SWI/SNF chromatin remodeling and cancer.

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• Malignant rhabdoid meningioma arising in the setting of preexisting ganglioglioma: a diagnosis supported by fluorescence in situ hybridization. Case report.

  2002cited by this paper
• Atypical teratoid/rhabdoid tumor of the central nervous system: Clinico‐pathological study

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• Chromatin remodeling factor encoded by ini1 induces G1 arrest and apoptosis in ini1-deficient cells

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• Congenital Disseminated Malignant Rhabdoid Tumor and Cerebellar Tumor Mimicking Medulloblastoma in Monozygotic Twins: Pathologic and Molecular Diagnosis

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• Highly penetrant, rapid tumorigenesis through conditional inversion of the tumor suppressor gene Snf5.

  2002cited by this paper
• Cytokeratin Subunits of Inclusion Bodies in Rhabdoid Cells: Immunohistochemical and Clinicopathological Study of Malignant Rhabdoid Tumor and Epithelioid Sarcoma

  2001cited by this paper
• Atypical Teratoid/rhabdoid Tumors in Adult Patients: Case Report and Review of the Literature

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• Comparative Immunohistochemical Study of Insulin-like Growth Factor II and Insulin-like Growth Factor ReceptorType 1 in Pediatric Brain Tumors

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• Rhabdoid Papillary Meningioma

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• Choroid Plexus Carcinomas and Rhabdoid Tumors: Phenotypic and Genotypic Overlap

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• Disruption of Ini1 Leads to Peri-Implantation Lethality and Tumorigenesis in Mice

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• Chromosome 22q dosage in composite extrarenal rhabdoid tumors: clonal evolution or a phenotypic mimic?

  2001cited by this paper
• Evidence of recurrent atypical meningioma with rhabdoid transformation and expression of pyrogenic cytokines in a child presenting with a marked acute-phase response: case report and review of the literature.

  2001cited by this paper
• Indications for a tumor suppressor gene at 22q11 involved in the pathogenesis of ependymal tumors and distinct from hSNF5/INI1

  2001cited by this paper
• Extraneural metastasis in a child with atypical teratoid rhabdoid tumor of the central nervous system

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• When the SWI/SNF complex remodels … the cell cycle

  2001cited by this paper
• Subcellular Distribution of Cytokeratin and Vimentin in Malignant Rhabdoid Tumor: Three-Dimensional Imaging with Confocal Laser Scanning Microscopy and Double Immunofluorescence

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• Mutational analysis of INI1 in sporadic human brain tumors

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• Atypical teratoid/rhabdoid tumor or medulloblastoma?

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• A role for fluorescence in situ hybridization detection of chromosome 22q dosage in distinguishing atypical teratoid/rhabdoid tumors from medulloblastoma/central primitive neuroectodermal tumors.

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• Tumors of the choroid plexus

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• Germline INI1 mutation in a patient with a central nervous system atypical teratoid tumor and renal rhabdoid tumor

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• The murine SNF5/INI1 chromatin remodeling factor is essential for embryonic development and tumor suppression

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• Exit from G1 and S phase of the cell cycle is regulated by repressor complexes containing HDAC-Rb-hSWI/SNF and Rb-hSWI/SNF.

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• A Brg1 null mutation in the mouse reveals functional differences among mammalian SWI/SNF complexes.

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• Haploinsufficiency of Snf5 (integrase interactor 1) predisposes to malignant rhabdoid tumors in mice.

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• Malignant Rhabdoid Tumor: A Phenotype? An Entity?—A Controversy Revisited

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• BRG1, a component of the SWI-SNF complex, is mutated in multiple human tumor cell lines.

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• Atypical teratoid/rhabdoid tumor of the central nervous system: a comparative study with primitive neuroectodermal tumor/medulloblastoma

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• Familial posterior fossa brain tumors of infancy secondary to germline mutation of the hSNF5 gene.

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• Mutations of the hSNF5/INI1 gene in renal rhabdoid tumors with second primary brain tumors.

  2000cited by this paper
• BRG-1 is required for RB-mediated cell cycle arrest.

  2000cited by this paper
• Primary malignant rhabdoid tumour of the brain in an adult

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• Atypical Teratoid Rhabdoid Tumor With TTF-1 Expression: A Case Report and Possible Insight Into Its Embryologic Origin.

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  2020cites this paper
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  2019cites this paper
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  2018cites this paper
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  2018cites this paper
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