HIC1 hypermethylation is a late event in hematopoietic neoplasms

Jean Pierre J. Issa, Barbara A. Zehnbauer, Scott H. Kaufmann, Maggie A. Biel, Stephen B. Baylin

Research output: Contribution to journalArticlepeer-review

98 Scopus citations

Abstract

HIC1, a candidate tumor suppressor gene on 17p13.3, is hypermethylated and silenced in a large number of solid tumors. To determine its potential role in leukemias, we studied its methylation status in normal and neoplastic hematopoietic cells. We found HIC1 to be unmethylated in peripheral blood cells, bone marrow cells, and CD34+ cells. HIC1 was rarely methylated in newly diagnosed acute myelogenous leukemias (10%) but was relatively frequently methylated in newly diagnosed non-Hodgkin's lymphoma (25%), acute lymphocytic leukemia (ALL; 53%), and chronic-phase chronic myelogenous leukemia (50%). By contrast, HIC1 was hypermethylated in 100% of recurrent ALL and 100% of blast crisis chronic myelogenous leukemia. In two patients with ALL for whom paired diagnosis/relapse samples were available, HIC1 was unmethylated at diagnosis but was highly methylated at relapse after a chemotherapy-induced complete remission. HIC1 methylation, therefore, seems to be a progression event in hematopoietic neoplasms.

Original languageEnglish (US)
Pages (from-to)1678-1681
Number of pages4
JournalCancer research
Volume57
Issue number9
StatePublished - May 1 1997

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Fingerprint Dive into the research topics of 'HIC1 hypermethylation is a late event in hematopoietic neoplasms'. Together they form a unique fingerprint.

Cite this