| Literature DB >> 16105758 |
Masashi Sawa1, Kazuhito Yamamoto, Toshiya Yokozawa, Hitoshi Kiyoi, Asahi Hishida, Tomohiro Kajiguchi, Masao Seto, Akio Kohno, Kunio Kitamura, Yoshie Itoh, Norio Asou, Nobuyuki Hamajima, Nobuhiko Emi, Tomoki Naoe.
Abstract
Recent studies have suggested that one of the polycomb group genes, BMI-1, has an important role in the maintenance of normal and leukemic stem cells by repressing the INK4a/ARF locus. Here, we quantitatively examined BMI-1 expression level in samples from patients with acute myeloid leukemia (AML) and other hematologic malignancies. Moderate to high BMI-1 expression was detected in AML patients, and the BMI-1 expression levels in AML samples were significantly higher than in normal bone marrow controls (P = .0011). Specimens of French-American-British classification subtype M0 showed higher relative expression of the BMI-1 transcript (median, 390.2 3 10(-3)) than the other subtypes (median, 139.0 3 10(-3)) (P < .0001). Leukemia other than AML showed low to moderate expression. INK4a-ARF transcript expression tended to be inverse proportion to that of BMI-1. In an M0 patient with a high BMI-1 transcript level, the INK4a-ARF transcript level fell promptly and maintained a low value after the patient achieved complete remission. These results indicated that a subgroup of M0 patients has a high expression level of polycomb group gene BMI-1, which may contribute to leukemogenesis.Entities:
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Year: 2005 PMID: 16105758 DOI: 10.1532/IJH97.05013
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490