Folate receptor type β is a neutrophilic lineage marker and is differentially expressed in myeloid leukemia

BACKGROUND The membrane‐associated folate receptor (FR) type β is elevated in the spleen in patients with chronic myeloid leukemia (CML) and acute myeloid leukemia (AML). In this study, the authors investigated possible cell type and differentiation stage specificity of expression of FR‐β in normal...

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Veröffentlicht in:Cancer 1999-01, Vol.85 (2), p.348-357
Hauptverfasser: Ross, John F., Wang, Hui, Behm, Frederick G., Mathew, Prasad, Wu, Marietta, Booth, Robert, Ratnam, Manohar
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container_end_page 357
container_issue 2
container_start_page 348
container_title Cancer
container_volume 85
creator Ross, John F.
Wang, Hui
Behm, Frederick G.
Mathew, Prasad
Wu, Marietta
Booth, Robert
Ratnam, Manohar
description BACKGROUND The membrane‐associated folate receptor (FR) type β is elevated in the spleen in patients with chronic myeloid leukemia (CML) and acute myeloid leukemia (AML). In this study, the authors investigated possible cell type and differentiation stage specificity of expression of FR‐β in normal and leukemic hematopoietic cells. METHODS An affinity‐purified rabbit polyclonal antibody specific for FR‐β was employed for immunostaining representative bone marrow smears and peripheral blood smears from normal individuals and from a limited number of patients with various leukemias. Multiple samples of normal bone marrow and peripheral blood were analyzed for the expression of FR‐β and selected CD antigens by two‐ or three‐color flow cytometry. RESULTS Of the morphologically identifiable cells, only neutrophils were positive for FR‐β. The leukemic blasts in CML patients showed expression of FR‐β with no apparent relation to the occurrence of the Philadelphia chromosome. Among acute nonlymphocytic leukemias, FR‐β was expressed in promyelocytic leukemia, in the myeloblast populations of myelomonocytic and erythroleukemias, and variably in M1/M2 AML. Neither the blasts of acute lymphocytic leukemia nor the more mature cells of chronic lymphocytic and hairy cell leukemias expressed FR‐β. The less differentiated FR‐β positive AML samples also were positive for CD34 and HLA‐DR. Flow cytometric analysis of normal bone marrow and peripheral blood revealed low or insignificant coexpression of FR‐β with CD34, CD19, and CD3, whereas significant coexpression was observed with high levels of CD33, CD13, and CD11b; coexpression of FR‐β with CD14 was high in the immature bone marrow cells, comparable to that in myeloid cells, but relatively low in peripheral blood. CONCLUSIONS The results of this study suggest a narrow expression pattern of FR‐β marking the neutrophilic lineage and the possibility of defining a subtype or subtypes of myeloid leukemia based on FR‐β expression. The identification of FR‐β positive leukemias and the absence of the receptor in normal CD34 positive cells may enable selective receptor‐mediated targeting of leukemic cells. Cancer 1999;85:348–57. © 1999 American Cancer Society. In normal hematopoiesis, expression of folate receptor type β is highest in late stages of neutrophilic differentiation and insignificant in CD34+ cells. High expression of the protein is observed in certain myeloid leukemia cells, suggesting its potential usefulness as a pr
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In this study, the authors investigated possible cell type and differentiation stage specificity of expression of FR‐β in normal and leukemic hematopoietic cells. METHODS An affinity‐purified rabbit polyclonal antibody specific for FR‐β was employed for immunostaining representative bone marrow smears and peripheral blood smears from normal individuals and from a limited number of patients with various leukemias. Multiple samples of normal bone marrow and peripheral blood were analyzed for the expression of FR‐β and selected CD antigens by two‐ or three‐color flow cytometry. RESULTS Of the morphologically identifiable cells, only neutrophils were positive for FR‐β. The leukemic blasts in CML patients showed expression of FR‐β with no apparent relation to the occurrence of the Philadelphia chromosome. Among acute nonlymphocytic leukemias, FR‐β was expressed in promyelocytic leukemia, in the myeloblast populations of myelomonocytic and erythroleukemias, and variably in M1/M2 AML. Neither the blasts of acute lymphocytic leukemia nor the more mature cells of chronic lymphocytic and hairy cell leukemias expressed FR‐β. The less differentiated FR‐β positive AML samples also were positive for CD34 and HLA‐DR. Flow cytometric analysis of normal bone marrow and peripheral blood revealed low or insignificant coexpression of FR‐β with CD34, CD19, and CD3, whereas significant coexpression was observed with high levels of CD33, CD13, and CD11b; coexpression of FR‐β with CD14 was high in the immature bone marrow cells, comparable to that in myeloid cells, but relatively low in peripheral blood. CONCLUSIONS The results of this study suggest a narrow expression pattern of FR‐β marking the neutrophilic lineage and the possibility of defining a subtype or subtypes of myeloid leukemia based on FR‐β expression. The identification of FR‐β positive leukemias and the absence of the receptor in normal CD34 positive cells may enable selective receptor‐mediated targeting of leukemic cells. Cancer 1999;85:348–57. © 1999 American Cancer Society. In normal hematopoiesis, expression of folate receptor type β is highest in late stages of neutrophilic differentiation and insignificant in CD34+ cells. High expression of the protein is observed in certain myeloid leukemia cells, suggesting its potential usefulness as a prognostic marker or a therapeutic target.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/(SICI)1097-0142(19990115)85:2&lt;348::AID-CNCR12&gt;3.0.CO;2-4</identifier><identifier>PMID: 10023702</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>New York: John Wiley &amp; Sons, Inc</publisher><subject>Animals ; Antigens, CD - analysis ; Antigens, Differentiation - biosynthesis ; Biological and medical sciences ; Biomarkers ; Blood/Bone Marrow ; Carrier Proteins - biosynthesis ; Carrier Proteins - immunology ; CD antigens ; Cell Differentiation ; CHO Cells ; Cricetinae ; differentiation marker ; folate receptor ; Folate Receptors, GPI-Anchored ; Hematologic and hematopoietic diseases ; Humans ; Immunohistochemistry ; leukemia ; Leukemia, Myeloid - metabolism ; Leukemia, Myeloid - pathology ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Leukocytes, Mononuclear - metabolism ; Medical sciences ; Neutrophils - cytology ; Rabbits ; Receptors, Cell Surface</subject><ispartof>Cancer, 1999-01, Vol.85 (2), p.348-357</ispartof><rights>Copyright © 1999 American Cancer Society</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2F%28SICI%291097-0142%2819990115%2985%3A2%3C348%3A%3AAID-CNCR12%3E3.0.CO%3B2-4$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291097-0142%2819990115%2985%3A2%3C348%3A%3AAID-CNCR12%3E3.0.CO%3B2-4$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27903,27904,45553,45554,46388,46812</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1664083$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10023702$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ross, John F.</creatorcontrib><creatorcontrib>Wang, Hui</creatorcontrib><creatorcontrib>Behm, Frederick G.</creatorcontrib><creatorcontrib>Mathew, Prasad</creatorcontrib><creatorcontrib>Wu, Marietta</creatorcontrib><creatorcontrib>Booth, Robert</creatorcontrib><creatorcontrib>Ratnam, Manohar</creatorcontrib><title>Folate receptor type β is a neutrophilic lineage marker and is differentially expressed in myeloid leukemia</title><title>Cancer</title><addtitle>Cancer</addtitle><description>BACKGROUND The membrane‐associated folate receptor (FR) type β is elevated in the spleen in patients with chronic myeloid leukemia (CML) and acute myeloid leukemia (AML). In this study, the authors investigated possible cell type and differentiation stage specificity of expression of FR‐β in normal and leukemic hematopoietic cells. METHODS An affinity‐purified rabbit polyclonal antibody specific for FR‐β was employed for immunostaining representative bone marrow smears and peripheral blood smears from normal individuals and from a limited number of patients with various leukemias. Multiple samples of normal bone marrow and peripheral blood were analyzed for the expression of FR‐β and selected CD antigens by two‐ or three‐color flow cytometry. RESULTS Of the morphologically identifiable cells, only neutrophils were positive for FR‐β. The leukemic blasts in CML patients showed expression of FR‐β with no apparent relation to the occurrence of the Philadelphia chromosome. Among acute nonlymphocytic leukemias, FR‐β was expressed in promyelocytic leukemia, in the myeloblast populations of myelomonocytic and erythroleukemias, and variably in M1/M2 AML. Neither the blasts of acute lymphocytic leukemia nor the more mature cells of chronic lymphocytic and hairy cell leukemias expressed FR‐β. The less differentiated FR‐β positive AML samples also were positive for CD34 and HLA‐DR. Flow cytometric analysis of normal bone marrow and peripheral blood revealed low or insignificant coexpression of FR‐β with CD34, CD19, and CD3, whereas significant coexpression was observed with high levels of CD33, CD13, and CD11b; coexpression of FR‐β with CD14 was high in the immature bone marrow cells, comparable to that in myeloid cells, but relatively low in peripheral blood. CONCLUSIONS The results of this study suggest a narrow expression pattern of FR‐β marking the neutrophilic lineage and the possibility of defining a subtype or subtypes of myeloid leukemia based on FR‐β expression. The identification of FR‐β positive leukemias and the absence of the receptor in normal CD34 positive cells may enable selective receptor‐mediated targeting of leukemic cells. Cancer 1999;85:348–57. © 1999 American Cancer Society. In normal hematopoiesis, expression of folate receptor type β is highest in late stages of neutrophilic differentiation and insignificant in CD34+ cells. High expression of the protein is observed in certain myeloid leukemia cells, suggesting its potential usefulness as a prognostic marker or a therapeutic target.</description><subject>Animals</subject><subject>Antigens, CD - analysis</subject><subject>Antigens, Differentiation - biosynthesis</subject><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>Blood/Bone Marrow</subject><subject>Carrier Proteins - biosynthesis</subject><subject>Carrier Proteins - immunology</subject><subject>CD antigens</subject><subject>Cell Differentiation</subject><subject>CHO Cells</subject><subject>Cricetinae</subject><subject>differentiation marker</subject><subject>folate receptor</subject><subject>Folate Receptors, GPI-Anchored</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>leukemia</subject><subject>Leukemia, Myeloid - metabolism</subject><subject>Leukemia, Myeloid - pathology</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Leukocytes, Mononuclear - metabolism</subject><subject>Medical sciences</subject><subject>Neutrophils - cytology</subject><subject>Rabbits</subject><subject>Receptors, Cell Surface</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkdtu1DAQhi0EotvCKyBfINReZPEhjpMtQlSBlpUqVuIgIW4srzMGU-eAnajktfogfaYm7Ba4smb8-R95PoTeULKkhLCXx5_W5fqEkkImhKbsmBZFQSgVJ7lYsVc8zVers_XbpPxQfqTsNV-SZbk5ZUn6AC3-PnqIFoSQPBEp_3qADmP8OZWSCf4YHcxDuCRsgfx563UPOICBrm8D7scO8O0NdhFr3MDQh7b74bwz2LsG9HfAtQ5XELBuqhmqnLUQoOmd9n7E8LsLECNMdw2uR_Ctq7CH4Qpqp5-gR1b7CE_35xH6cv7uc_k-udxcrMuzy6TjtGAJBaCa0UrwbGu1tkxkmmbGZoVMt3ILmtlMSMkBjGTA0sJQSvOccW4ranLBj9CLXW4X2l8DxF7VLhrwXjfQDlFlhZAZ5zP4bA8O2xoq1QU3_W5U9_uZgOd7QEejvQ26MS7-47IsJTmfsG877Np5GP-L-ZOkZptqFqNmMerepsqFYmqyqSaZaidTcUVUuZn66b7D7wDVp5lB</recordid><startdate>19990115</startdate><enddate>19990115</enddate><creator>Ross, John F.</creator><creator>Wang, Hui</creator><creator>Behm, Frederick G.</creator><creator>Mathew, Prasad</creator><creator>Wu, Marietta</creator><creator>Booth, Robert</creator><creator>Ratnam, Manohar</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley-Liss</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19990115</creationdate><title>Folate receptor type β is a neutrophilic lineage marker and is differentially expressed in myeloid leukemia</title><author>Ross, John F. ; Wang, Hui ; Behm, Frederick G. ; Mathew, Prasad ; Wu, Marietta ; Booth, Robert ; Ratnam, Manohar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p3192-1ee1a21d536bfaaf256a16cf6974b7bea2f65773eec72e249c11188233fd1c853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Antigens, CD - analysis</topic><topic>Antigens, Differentiation - biosynthesis</topic><topic>Biological and medical sciences</topic><topic>Biomarkers</topic><topic>Blood/Bone Marrow</topic><topic>Carrier Proteins - biosynthesis</topic><topic>Carrier Proteins - immunology</topic><topic>CD antigens</topic><topic>Cell Differentiation</topic><topic>CHO Cells</topic><topic>Cricetinae</topic><topic>differentiation marker</topic><topic>folate receptor</topic><topic>Folate Receptors, GPI-Anchored</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>leukemia</topic><topic>Leukemia, Myeloid - metabolism</topic><topic>Leukemia, Myeloid - pathology</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Leukocytes, Mononuclear - metabolism</topic><topic>Medical sciences</topic><topic>Neutrophils - cytology</topic><topic>Rabbits</topic><topic>Receptors, Cell Surface</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ross, John F.</creatorcontrib><creatorcontrib>Wang, Hui</creatorcontrib><creatorcontrib>Behm, Frederick G.</creatorcontrib><creatorcontrib>Mathew, Prasad</creatorcontrib><creatorcontrib>Wu, Marietta</creatorcontrib><creatorcontrib>Booth, Robert</creatorcontrib><creatorcontrib>Ratnam, Manohar</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ross, John F.</au><au>Wang, Hui</au><au>Behm, Frederick G.</au><au>Mathew, Prasad</au><au>Wu, Marietta</au><au>Booth, Robert</au><au>Ratnam, Manohar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Folate receptor type β is a neutrophilic lineage marker and is differentially expressed in myeloid leukemia</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>1999-01-15</date><risdate>1999</risdate><volume>85</volume><issue>2</issue><spage>348</spage><epage>357</epage><pages>348-357</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>BACKGROUND The membrane‐associated folate receptor (FR) type β is elevated in the spleen in patients with chronic myeloid leukemia (CML) and acute myeloid leukemia (AML). In this study, the authors investigated possible cell type and differentiation stage specificity of expression of FR‐β in normal and leukemic hematopoietic cells. METHODS An affinity‐purified rabbit polyclonal antibody specific for FR‐β was employed for immunostaining representative bone marrow smears and peripheral blood smears from normal individuals and from a limited number of patients with various leukemias. Multiple samples of normal bone marrow and peripheral blood were analyzed for the expression of FR‐β and selected CD antigens by two‐ or three‐color flow cytometry. RESULTS Of the morphologically identifiable cells, only neutrophils were positive for FR‐β. The leukemic blasts in CML patients showed expression of FR‐β with no apparent relation to the occurrence of the Philadelphia chromosome. Among acute nonlymphocytic leukemias, FR‐β was expressed in promyelocytic leukemia, in the myeloblast populations of myelomonocytic and erythroleukemias, and variably in M1/M2 AML. Neither the blasts of acute lymphocytic leukemia nor the more mature cells of chronic lymphocytic and hairy cell leukemias expressed FR‐β. The less differentiated FR‐β positive AML samples also were positive for CD34 and HLA‐DR. Flow cytometric analysis of normal bone marrow and peripheral blood revealed low or insignificant coexpression of FR‐β with CD34, CD19, and CD3, whereas significant coexpression was observed with high levels of CD33, CD13, and CD11b; coexpression of FR‐β with CD14 was high in the immature bone marrow cells, comparable to that in myeloid cells, but relatively low in peripheral blood. CONCLUSIONS The results of this study suggest a narrow expression pattern of FR‐β marking the neutrophilic lineage and the possibility of defining a subtype or subtypes of myeloid leukemia based on FR‐β expression. The identification of FR‐β positive leukemias and the absence of the receptor in normal CD34 positive cells may enable selective receptor‐mediated targeting of leukemic cells. Cancer 1999;85:348–57. © 1999 American Cancer Society. In normal hematopoiesis, expression of folate receptor type β is highest in late stages of neutrophilic differentiation and insignificant in CD34+ cells. High expression of the protein is observed in certain myeloid leukemia cells, suggesting its potential usefulness as a prognostic marker or a therapeutic target.</abstract><cop>New York</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>10023702</pmid><doi>10.1002/(SICI)1097-0142(19990115)85:2&lt;348::AID-CNCR12&gt;3.0.CO;2-4</doi><tpages>10</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Wiley Free Content; Alma/SFX Local Collection
subjects Animals
Antigens, CD - analysis
Antigens, Differentiation - biosynthesis
Biological and medical sciences
Biomarkers
Blood/Bone Marrow
Carrier Proteins - biosynthesis
Carrier Proteins - immunology
CD antigens
Cell Differentiation
CHO Cells
Cricetinae
differentiation marker
folate receptor
Folate Receptors, GPI-Anchored
Hematologic and hematopoietic diseases
Humans
Immunohistochemistry
leukemia
Leukemia, Myeloid - metabolism
Leukemia, Myeloid - pathology
Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
Leukocytes, Mononuclear - metabolism
Medical sciences
Neutrophils - cytology
Rabbits
Receptors, Cell Surface
title Folate receptor type β is a neutrophilic lineage marker and is differentially expressed in myeloid leukemia
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