Clinicopathologic and survival correlates of embryonal rhabdomyosarcoma driven by RAS / RAF mutations-Reference-Cited by-同舟云学术

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Clinicopathologic and survival correlates of embryonal rhabdomyosarcoma driven by RAS / RAF mutations

Published:2021-11-16 Issue:3 Volume:61 Page:131-137
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosomes & Cancer

Author:

Agaram Narasimhan P.¹^ORCID,Huang Shih‐Chiang²,Tap William D.³,Wexler Leonard H.⁴,Antonescu Cristina R.¹^ORCID

Affiliation:

1. Department of Pathology Memorial Sloan Kettering Cancer Center New York New York USA

2. Department of Anatomic Pathology, Linkou Chang Gung Memorial Hospital Chang Gung University College of Medicine Taoyuan Taiwan

3. Department of Medicine Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College New York New York USA

4. Department of Pediatrics Memorial Sloan Kettering Cancer Center New York New York USA

Publisher

Wiley

Subject

Cancer Research,Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/gcc.23010

Reference26 articles.

1. Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma

2. Comprehensive Genomic Analysis of Rhabdomyosarcoma Reveals a Landscape of Alterations Affecting a Common Genetic Axis in Fusion-Positive and Fusion-Negative Tumors

3. Genomic Classification and Clinical Outcome in Rhabdomyosarcoma: A Report From an International Consortium

4. Rhabdomyosarcoma: Review of the Children's Oncology Group (COG) soft-tissue Sarcoma committee experience and rationale for current COG studies

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1. Preclinical evidence for employing MEK inhibition in NRAS mutated pediatric gastroenteropancreatic neuroendocrine-like tumors;Translational Oncology;2024-09

2. Botryoid-type Embryonal Rhabdomyosarcoma;American Journal of Surgical Pathology;2024-08-30

3. NF1-Driven Rhabdomyosarcoma Phenotypes: A Comparative Clinical and Molecular Study of NF1-Mutant Rhabdomyosarcoma and NF1-Associated Malignant Triton Tumor;JCO Precision Oncology;2024-04

4. The RRAS2 pathogenic variant (c.67G>T; p. Gly23Cys) produces Noonan syndrome with embryonal rhabdomyosarcoma;Molecular Genetics & Genomic Medicine;2023-11-09

5. Case Report: Sequential postzygotic HRAS mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving HRAS in oncogenic transformation;Frontiers in Genetics;2023-08-10

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