KAT6B Is a Tumor Suppressor Histone H3 Lysine 23 Acetyltransferase Undergoing Genomic Loss in Small Cell Lung Cancer

Cancer Res. 2015 Sep 15;75(18):3936-45. doi: 10.1158/0008-5472.CAN-14-3702. Epub 2015 Jul 24.

Abstract

Recent efforts to sequence human cancer genomes have highlighted that point mutations in genes involved in the epigenetic setting occur in tumor cells. Small cell lung cancer (SCLC) is an aggressive tumor with poor prognosis, where little is known about the genetic events related to its development. Herein, we have identified the presence of homozygous deletions of the candidate histone acetyltransferase KAT6B, and the loss of the corresponding transcript, in SCLC cell lines and primary tumors. Furthermore, we show, in vitro and in vivo, that the depletion of KAT6B expression enhances cancer growth, while its restoration induces tumor suppressor-like features. Most importantly, we demonstrate that KAT6B exerts its tumor-inhibitory role through a newly defined type of histone H3 Lys23 acetyltransferase activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Animals
  • Antineoplastic Agents, Alkylating / pharmacology
  • Antineoplastic Agents, Alkylating / therapeutic use
  • Camptothecin / analogs & derivatives
  • Camptothecin / pharmacology
  • Camptothecin / therapeutic use
  • Carcinoma, Small Cell / drug therapy
  • Carcinoma, Small Cell / enzymology*
  • Carcinoma, Small Cell / genetics
  • Carcinoma, Small Cell / pathology
  • Cell Line, Tumor
  • Chromatin Immunoprecipitation
  • Drug Resistance, Neoplasm
  • Gene Deletion
  • Gene Expression Profiling
  • Genes, Tumor Suppressor
  • Heterografts
  • Histone Acetyltransferases / deficiency
  • Histone Acetyltransferases / genetics
  • Histone Acetyltransferases / physiology*
  • Histones / metabolism
  • Humans
  • Irinotecan
  • Lung Neoplasms / drug therapy
  • Lung Neoplasms / enzymology*
  • Lung Neoplasms / genetics
  • Lung Neoplasms / pathology
  • Mice
  • Mice, Nude
  • Neoplasm Metastasis
  • Neoplasm Proteins / deficiency
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / physiology*
  • Protein Processing, Post-Translational
  • RNA Interference
  • RNA, Messenger / genetics
  • RNA, Neoplasm / genetics
  • RNA, Small Interfering / pharmacology

Substances

  • Antineoplastic Agents, Alkylating
  • Histones
  • Neoplasm Proteins
  • RNA, Messenger
  • RNA, Neoplasm
  • RNA, Small Interfering
  • Irinotecan
  • Histone Acetyltransferases
  • KAT6B protein, human
  • Camptothecin