Dominant Gene Expression Profiles Define Adenoid Cystic Carcinoma (ACC) from Different Tissues: Validation of a Gene Signature Classifier for Poor Survival in Salivary Gland ACC

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  • Kathryn J. Brayer
  • Huining Kang
  • Adel K. El-Naggar
  • Simon Andreasen
  • Homøe, Preben
  • Katalin Kiss
  • Lauge Mikkelsen
  • Heegaard, Steffen
  • Daniel Pelaez
  • Acadia Moeyersoms
  • David T. Tse
  • Yan Guo
  • David Y. Lee
  • Scott A. Ness

Adenoid cystic carcinoma (ACC) is an aggressive malignancy that most often arises in salivary or lacrimal glands but can also occur in other tissues. We used optimized RNA-sequencing to analyze the transcriptomes of 113 ACC tumor samples from salivary gland, lacrimal gland, breast or skin. ACC tumors from different organs displayed remarkedly similar transcription profiles, and most harbored translocations in the MYB or MYBL1 genes, which encode oncogenic transcription factors that may induce dramatic genetic and epigenetic changes leading to a dominant ‘ACC phenotype’. Further analysis of the 56 salivary gland ACC tumors led to the identification of three distinct groups of patients, based on gene expression profiles, including one group with worse survival. We tested whether this new cohort could be used to validate a biomarker developed previously with a different set of 68 ACC tumor samples. Indeed, a 49-gene classifier developed with the earlier cohort correctly identified 98% of the poor survival patients from the new set, and a 14-gene classifier was almost as accurate. These validated biomarkers form a platform to identify and stratify high-risk ACC patients into clinical trials of targeted therapies for sustained clinical response.

OriginalsprogEngelsk
Artikelnummer1390
TidsskriftCancers
Vol/bind15
Udgave nummer5
Antal sider21
ISSN2072-6694
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
The RNA-seq analysis was partially supported by UNM Comprehensive Cancer Center Support Grant from NIH NCI P30CA118100. K.J.B. and S.A.N. were partially supported by grants from the Adenoid Cystic Carcinoma Research Foundation and from NIH NIDCR R01DE023222 (to S.A.N.). The DK studies were substantially supported by Region Zealand’s Research Fund.

Publisher Copyright:
© 2023 by the authors.

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