Literature DB >> 29972784

Integrative Bayesian Analysis Identifies Rhabdomyosarcoma Disease Genes.

Lin Xu1, Yanbin Zheng2, Jing Liu3, Dinesh Rakheja4, Sydney Singleterry3, Theodore W Laetsch5, Jack F Shern6, Javed Khan7, Timothy J Triche8, Douglas S Hawkins9, James F Amatruda10, Stephen X Skapek11.   

Abstract

Identifying oncogenic drivers and tumor suppressors remains a challenge in many forms of cancer, including rhabdomyosarcoma. Anticipating gene expression alterations resulting from DNA copy-number variants to be particularly important, we developed a computational and experimental strategy incorporating a Bayesian algorithm and CRISPR/Cas9 "mini-pool" screen that enables both genome-scale assessment of disease genes and functional validation. The algorithm, called iExCN, identified 29 rhabdomyosarcoma drivers and suppressors enriched for cell-cycle and nucleic-acid-binding activities. Functional studies showed that many iExCN genes represent rhabdomyosarcoma line-specific or shared vulnerabilities. Complementary experiments addressed modes of action and demonstrated coordinated repression of multiple iExCN genes during skeletal muscle differentiation. Analysis of two separate cohorts revealed that the number of iExCN genes harboring copy-number alterations correlates with survival. Our findings highlight rhabdomyosarcoma as a cancer in which multiple drivers influence disease biology and demonstrate a generalizable capacity for iExCN to unmask disease genes in cancer.
Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Bayesian algorithm; CRISPR/Cas9; childhood cancer; integrative genomic analysis; oncogene; rhabdomyosarcoma; tumor suppressor gene

Mesh:

Substances:

Year:  2018        PMID: 29972784      PMCID: PMC7293769          DOI: 10.1016/j.celrep.2018.06.006

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  50 in total

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

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8.  Targeting wild-type and mutationally activated FGFR4 in rhabdomyosarcoma with the inhibitor ponatinib (AP24534).

Authors:  Samuel Q Li; Adam T Cheuk; Jack F Shern; Young K Song; Laura Hurd; Hongling Liao; Jun S Wei; Javed Khan
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Authors: 
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Journal:  Pediatr Blood Cancer       Date:  2019-06-21       Impact factor: 3.167

2.  Bayesian Modeling Identifies PLAG1 as a Key Regulator of Proliferation and Survival in Rhabdomyosarcoma Cells.

Authors:  Yanbin Zheng; Lin Xu; Mohammed Hassan; Xiaoyun Zhou; Qinbo Zhou; Dinesh Rakheja; Stephen X Skapek
Journal:  Mol Cancer Res       Date:  2019-11-22       Impact factor: 5.852

3.  A Step Forward in Realizing the Promise of Genomic Medicine for Childhood Rhabdomyosarcoma.

Authors:  Leo Mascarenhas
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Journal:  Genes Dev       Date:  2019-04-11       Impact factor: 11.361

Review 5.  Applications of CRISPR/Cas9 in the research of malignant musculoskeletal tumors.

Authors:  Wei Liu; Shubin Wang; Binhui Lin; Wei Zhang; Guangrong Ji
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Review 6.  Non-coding RNA in rhabdomyosarcoma progression and metastasis.

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7.  DCX and CRABP2 are candidate genes for differential diagnosis between pre-chemotherapy embryonic and alveolar rhabdomyosarcoma in pediatric patients.

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Journal:  Pediatr Investig       Date:  2021-06-18

8.  Epigenetic regulator BMI1 promotes alveolar rhabdomyosarcoma proliferation and constitutes a novel therapeutic target.

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  8 in total

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