Establishment of a novel human acute myeloblastic leukemia cell line (ynh-1) with t(16;21), t(1;16) and 12q13 translocations

Establishment of a novel human acute myeloblastic leukemia cell line (ynh-1) with t(16;21), t(1;16) and 12q13 translocations


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ABSTRACT The t(16;21)(p11;q22) translocation is a non-random chromosomal aberration observed in several types of human acute myeloblastic leukemia (AML), whereas the der(16)t(1;16) and


chromosome rearrangements at 12q13 are frequently found in solid tumors. A novel cell line YNH-1 was established from peripheral blood cells of a 46-year-old male with AML (M1) carrying


t(16;21) and t(1;16) translocations. YNH-1 has been maintained with a doubling time of 82 h for more than 20 months as a granulocyte colony-stimulating factor (G-CSF), granulocyte–macrophage


colony-stimulating factor (GM-CSF) and interleukin-3 (IL-3) dependent line. Morphologically YNH-1 cells were free-floating immature myeloblasts with lobulated nuclei and vacuoles in the


cytoplasm. They were positive for myeloperoxidase but negative for α-naphthyl butylate esterase and chloroacetate esterase stainings. In surface marker analysis YNH-1 cells were positive for


CD13, CD33 and CD34. Chromosomal analysis showed 46, XY, der(16)t(16;21)(p11;q22)t(1;16) (q12;q13), der(21)t(16;21)(p11;q22), der(6)t(6;12)(q13;q13), der(12)t(6;12)(q21;q13). These


translocations were confirmed by fluorescence _in situ_ hybridization (FISH) studies with the _ERG_-YAC clone and chromosome-specific DNA libraries. Both the _FUS/ERG_ and _ERG/FUS_ chimeric


transcripts were identified by reverse transcriptase-polymerase chain reaction (RT-PCR) analysis. Thus, YNH-1 could be a useful tool for elucidating the pathophysiology and molecular


mechanism in AML with t(16;21),t(1;16) and 12q13 translocations. Access through your institution Buy or subscribe This is a preview of subscription content, access via your institution


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2023 AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Department of Hematology, Musashino Red Cross Hospital, Tokyo, Japan K Yamamoto, H Hamaguchi & K Nagata * SRL, Inc, Tokyo, Japan M


Kobayashi & F Tanimoto * Third Department of Internal Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan M Taniwaki Authors * K Yamamoto View author publications You can


also search for this author inPubMed Google Scholar * H Hamaguchi View author publications You can also search for this author inPubMed Google Scholar * K Nagata View author publications You


can also search for this author inPubMed Google Scholar * M Kobayashi View author publications You can also search for this author inPubMed Google Scholar * F Tanimoto View author


publications You can also search for this author inPubMed Google Scholar * M Taniwaki View author publications You can also search for this author inPubMed Google Scholar RIGHTS AND


PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Yamamoto, K., Hamaguchi, H., Nagata, K. _et al._ Establishment of a novel human acute myeloblastic leukemia cell


line (YNH-1) with t(16;21), t(1;16) and 12q13 translocations. _Leukemia_ 11, 599–608 (1997). https://doi.org/10.1038/sj.leu.2400594 Download citation * Received: 25 September 1996 *


Accepted: 09 December 1996 * Issue Date: 01 April 1997 * DOI: https://doi.org/10.1038/sj.leu.2400594 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this


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KEYWORDS * acute myeloblastic leukemia * chromosome translocation * t(16;21) * _FUS/ERG_ transcripts * t(1;16) * 12q13