학술논문

NSD1- and NSD2-damaging mutations define a subset of laryngeal tumors with favorable prognosis.
Document Type
article
Source
Nature communications. 8(1)
Subject
Humans
Laryngeal Neoplasms
Histone-Lysine N-Methyltransferase
Intracellular Signaling Peptides and Proteins
Nuclear Proteins
Repressor Proteins
Prognosis
Cohort Studies
Gene Expression Regulation
Neoplastic
Mutation
Adult
Aged
Aged
80 and over
Middle Aged
Female
Male
Squamous Cell Carcinoma of Head and Neck
Histone Methyltransferases
and over
Gene Expression Regulation
Neoplastic
Language
Abstract
Squamous cell carcinomas of the head and neck (SCCHN) affect anatomical sites including the oral cavity, nasal cavity, pharynx, and larynx. Laryngeal cancers are characterized by high recurrence and poor overall survival, and currently lack robust molecular prognostic biomarkers for treatment stratification. Using an algorithm for integrative clustering that simultaneously assesses gene expression, somatic mutation, copy number variation, and methylation, we for the first time identify laryngeal cancer subtypes with distinct prognostic outcomes, and differing from the non-prognostic laryngeal subclasses reported by The Cancer Genome Atlas (TCGA). Although most common laryngeal gene mutations are found in both subclasses, better prognosis is strongly associated with damaging mutations of the methyltransferases NSD1 and NSD2, with findings confirmed in an independent validation cohort consisting of 63 laryngeal cancer patients. Intriguingly, NSD1/2 mutations are not prognostic for nonlaryngeal SCCHN. These results provide an immediately useful clinical metric for patient stratification and prognostication.