NELFE-Dependent MYC Signature Identifies a Unique Cancer Subtype in Hepatocellular Carcinoma.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
04 03 2019
Historique:
received: 19 10 2018
accepted: 29 01 2019
entrez: 6 3 2019
pubmed: 6 3 2019
medline: 23 9 2020
Statut: epublish

Résumé

The MYC oncogene is dysregulated in approximately 30% of liver cancer. In an effort to exploit MYC as a therapeutic target, including in hepatocellular carcinoma (HCC), strategies have been developed on the basis of MYC amplification or gene translocation. Due to the failure of these strategies to provide accurate diagnostics and prognostic value, we have developed a Negative Elongation Factor E (NELFE)-Dependent MYC Target (NDMT) gene signature. This signature, which consists of genes regulated by MYC and NELFE, an RNA binding protein that enhances MYC-induced hepatocarcinogenesis, is predictive of NELFE/MYC-driven tumors that would otherwise not be identified by gene amplification or translocation alone. We demonstrate the utility of the NDMT gene signature to predict a unique subtype of HCC, which is associated with a poor prognosis in three independent cohorts encompassing diverse etiologies, demographics, and viral status. The application of gene signatures, such as the NDMT signature, offers patients access to personalized risk assessments, which may be utilized to direct future care.

Identifiants

pubmed: 30833661
doi: 10.1038/s41598-019-39727-9
pii: 10.1038/s41598-019-39727-9
pmc: PMC6399236
doi:

Substances chimiques

Transcription Factors 0
negative elongation factor 0

Types de publication

Journal Article Research Support, N.I.H., Intramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

3369

Subventions

Organisme : Intramural NIH HHS
ID : Z01 BC010876
Pays : United States
Organisme : Intramural NIH HHS
ID : Z01 BC010877
Pays : United States

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Auteurs

Hien Dang (H)

Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, United States. hien.dang@jefferson.edu.
Department of Surgery, Division of Surgical Research, Thomas Jefferson University, Philadelphia, PA, United States. hien.dang@jefferson.edu.

Yotsawat Pomyen (Y)

Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, United States.
Translational Research Unit, Chulabhorn Research Institute, Bangkok, 10210, Thailand.

Sean P Martin (SP)

Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, United States.

Dana A Dominguez (DA)

Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, United States.

Sun Young Yim (SY)

Department of Systems Biology, Division of Cancer Medicine, UT MDACC, Houston, TX, United States.

Ju-Seog Lee (JS)

Department of Systems Biology, Division of Cancer Medicine, UT MDACC, Houston, TX, United States.

Anuradha Budhu (A)

Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, United States.

Ashesh P Shah (AP)

Department of Surgery, Division of Transplantation, Thomas Jefferson University, Philadelphia, PA, United States.

Adam S Bodzin (AS)

Department of Surgery, Division of Transplantation, Thomas Jefferson University, Philadelphia, PA, United States.

Xin Wei Wang (XW)

Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, United States. xw3u@nih.gov.

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