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DNA ploidy patterns and cytokinetics of non-Hodgkin's lymphoma
Flow cytometry studies for cellular DNA analysis were performed in 115 cases of non-Hodgkin's lymphoma, 53 of which had not received any prior chemotherapy or radiotherapy. DNA content was measured in ethanol fixed cells stained with chromomycin A3. According to the criteria of the Internationa...
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Published in: | Journal of clinical pathology 1986-09, Vol.39 (9), p.987-992 |
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description | Flow cytometry studies for cellular DNA analysis were performed in 115 cases of non-Hodgkin's lymphoma, 53 of which had not received any prior chemotherapy or radiotherapy. DNA content was measured in ethanol fixed cells stained with chromomycin A3. According to the criteria of the International Working Formulation there were 43 low grade, 58 intermediate grade, and eight high grade lymphomas; six cases were in the miscellaneous group. Seventy seven (67%) had only diploid DNA content. Thirty eight (33%) showed DNA aneuploidy; 20 of these had been previously treated with chemotherapy or radiotherapy, or both. DNA aneuploidy was seen as hyperdiploidy in all cases except one, and it varied from slightly hyperdiploid to tetraploid. The incidence of aneuploidy increased significantly with increasing histological grade (p = 0.0002) and was not related to previous treatment. The low, intermediate, and high grade lymphomas had 14% (six of 43), 47% (27 of 58), and 62.5% (five of eight) cases, respectively, that showed DNA aneuploidy. The percentage of cells in S phase increased significantly with a higher histological grade (p less than 0.0001). The median S fraction in the low, intermediate, and high grade lymphomas was 1.0 (0.5 to 10)% 4 (0.4 to 35)%, and 27 (4.6-56)%, respectively. There is a significant correlation between histological grade and S fraction and the presence or absence of aneuploidy. There is heterogeneity, however, within both histological grade and a histological subtype. |
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DNA content was measured in ethanol fixed cells stained with chromomycin A3. According to the criteria of the International Working Formulation there were 43 low grade, 58 intermediate grade, and eight high grade lymphomas; six cases were in the miscellaneous group. Seventy seven (67%) had only diploid DNA content. Thirty eight (33%) showed DNA aneuploidy; 20 of these had been previously treated with chemotherapy or radiotherapy, or both. DNA aneuploidy was seen as hyperdiploidy in all cases except one, and it varied from slightly hyperdiploid to tetraploid. The incidence of aneuploidy increased significantly with increasing histological grade (p = 0.0002) and was not related to previous treatment. The low, intermediate, and high grade lymphomas had 14% (six of 43), 47% (27 of 58), and 62.5% (five of eight) cases, respectively, that showed DNA aneuploidy. The percentage of cells in S phase increased significantly with a higher histological grade (p less than 0.0001). The median S fraction in the low, intermediate, and high grade lymphomas was 1.0 (0.5 to 10)% 4 (0.4 to 35)%, and 27 (4.6-56)%, respectively. There is a significant correlation between histological grade and S fraction and the presence or absence of aneuploidy. There is heterogeneity, however, within both histological grade and a histological subtype.</description><identifier>ISSN: 0021-9746</identifier><identifier>EISSN: 1472-4146</identifier><identifier>DOI: 10.1136/jcp.39.9.987</identifier><identifier>PMID: 3760241</identifier><identifier>CODEN: JCPAAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher><subject>Aneuploidy ; Biological and medical sciences ; DNA, Neoplasm - genetics ; Flow Cytometry ; Hematologic and hematopoietic diseases ; Humans ; Interphase ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Lymphoma - ultrastructure ; Medical sciences</subject><ispartof>Journal of clinical pathology, 1986-09, Vol.39 (9), p.987-992</ispartof><rights>1987 INIST-CNRS</rights><rights>Copyright BMJ Publishing Group LTD Sep 1986</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b505t-fa81b7f1c25b9b3a995e5ed9d2ec01c925a7db00f391e21e5ca3fac0816aae063</citedby><cites>FETCH-LOGICAL-b505t-fa81b7f1c25b9b3a995e5ed9d2ec01c925a7db00f391e21e5ca3fac0816aae063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC500198/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC500198/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7906073$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3760241$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Juneja, S K</creatorcontrib><creatorcontrib>Cooper, I A</creatorcontrib><creatorcontrib>Hodgson, G S</creatorcontrib><creatorcontrib>Wolf, M M</creatorcontrib><creatorcontrib>Ding, J C</creatorcontrib><creatorcontrib>Ironside, P N</creatorcontrib><creatorcontrib>Thomas, R J</creatorcontrib><creatorcontrib>Parkin, J D</creatorcontrib><title>DNA ploidy patterns and cytokinetics of non-Hodgkin's lymphoma</title><title>Journal of clinical pathology</title><addtitle>J Clin Pathol</addtitle><description>Flow cytometry studies for cellular DNA analysis were performed in 115 cases of non-Hodgkin's lymphoma, 53 of which had not received any prior chemotherapy or radiotherapy. DNA content was measured in ethanol fixed cells stained with chromomycin A3. According to the criteria of the International Working Formulation there were 43 low grade, 58 intermediate grade, and eight high grade lymphomas; six cases were in the miscellaneous group. Seventy seven (67%) had only diploid DNA content. Thirty eight (33%) showed DNA aneuploidy; 20 of these had been previously treated with chemotherapy or radiotherapy, or both. DNA aneuploidy was seen as hyperdiploidy in all cases except one, and it varied from slightly hyperdiploid to tetraploid. The incidence of aneuploidy increased significantly with increasing histological grade (p = 0.0002) and was not related to previous treatment. The low, intermediate, and high grade lymphomas had 14% (six of 43), 47% (27 of 58), and 62.5% (five of eight) cases, respectively, that showed DNA aneuploidy. The percentage of cells in S phase increased significantly with a higher histological grade (p less than 0.0001). The median S fraction in the low, intermediate, and high grade lymphomas was 1.0 (0.5 to 10)% 4 (0.4 to 35)%, and 27 (4.6-56)%, respectively. There is a significant correlation between histological grade and S fraction and the presence or absence of aneuploidy. There is heterogeneity, however, within both histological grade and a histological subtype.</description><subject>Aneuploidy</subject><subject>Biological and medical sciences</subject><subject>DNA, Neoplasm - genetics</subject><subject>Flow Cytometry</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Interphase</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Lymphoma - ultrastructure</subject><subject>Medical sciences</subject><issn>0021-9746</issn><issn>1472-4146</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><recordid>eNp9kUFP3DAQha0KBFvg1mulSFTl0mztOLbjA5XotrBIiF5oD1ysieOAl8RO7WzV_ff1alerwgHNwdK8b8Zv9BB6R_CUEMo_L_QwpXKaqhJv0ISUoshLUvI9NMG4ILkUJT9Eb2NcYEyoIPQAHVDBcVGSCfry7fYiGzpvm1U2wDia4GIGrsn0avRP1pnR6pj5NnPe5XPfPKTeWcy6VT88-h6O0X4LXTQn2_cI_bz8fjeb5zc_rq5nFzd5zTAb8xYqUouW6ILVsqYgJTPMNLIpjMZEy4KBaGqMWyqJKYhhGmgLGleEAxjM6RE63-wdlnVvGm3cGKBTQ7A9hJXyYNVzxdlH9eD_KJZullWa_7idD_730sRR9TZq03XgjF9GJQRmJRfrj05fgAu_DC7dpkiCSloIvqY-bSgdfIzBtDsnBKt1KCqFoqhUqSqR8Pf_u9_B2xSS_mGrQ9TQtQGctnGHCYk5FjRh-QazcTR_dzKEJ8UFFUzd_pqpr_eX1XwuqbpP_NmGr_vF6wb_AQhAsQc</recordid><startdate>19860901</startdate><enddate>19860901</enddate><creator>Juneja, S K</creator><creator>Cooper, I A</creator><creator>Hodgson, G S</creator><creator>Wolf, M M</creator><creator>Ding, J C</creator><creator>Ironside, P N</creator><creator>Thomas, R J</creator><creator>Parkin, J D</creator><general>BMJ Publishing Group Ltd and Association of Clinical Pathologists</general><general>BMJ</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19860901</creationdate><title>DNA ploidy patterns and cytokinetics of non-Hodgkin's lymphoma</title><author>Juneja, S K ; Cooper, I A ; Hodgson, G S ; Wolf, M M ; Ding, J C ; Ironside, P N ; Thomas, R J ; Parkin, J D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b505t-fa81b7f1c25b9b3a995e5ed9d2ec01c925a7db00f391e21e5ca3fac0816aae063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Aneuploidy</topic><topic>Biological and medical sciences</topic><topic>DNA, Neoplasm - genetics</topic><topic>Flow Cytometry</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Interphase</topic><topic>Leukemias. 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Myelofibrosis</topic><topic>Lymphoma - ultrastructure</topic><topic>Medical sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Juneja, S K</creatorcontrib><creatorcontrib>Cooper, I A</creatorcontrib><creatorcontrib>Hodgson, G S</creatorcontrib><creatorcontrib>Wolf, M M</creatorcontrib><creatorcontrib>Ding, J C</creatorcontrib><creatorcontrib>Ironside, P N</creatorcontrib><creatorcontrib>Thomas, R J</creatorcontrib><creatorcontrib>Parkin, J D</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Juneja, S K</au><au>Cooper, I A</au><au>Hodgson, G S</au><au>Wolf, M M</au><au>Ding, J C</au><au>Ironside, P N</au><au>Thomas, R J</au><au>Parkin, J D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DNA ploidy patterns and cytokinetics of non-Hodgkin's lymphoma</atitle><jtitle>Journal of clinical pathology</jtitle><addtitle>J Clin Pathol</addtitle><date>1986-09-01</date><risdate>1986</risdate><volume>39</volume><issue>9</issue><spage>987</spage><epage>992</epage><pages>987-992</pages><issn>0021-9746</issn><eissn>1472-4146</eissn><coden>JCPAAK</coden><abstract>Flow cytometry studies for cellular DNA analysis were performed in 115 cases of non-Hodgkin's lymphoma, 53 of which had not received any prior chemotherapy or radiotherapy. DNA content was measured in ethanol fixed cells stained with chromomycin A3. According to the criteria of the International Working Formulation there were 43 low grade, 58 intermediate grade, and eight high grade lymphomas; six cases were in the miscellaneous group. Seventy seven (67%) had only diploid DNA content. Thirty eight (33%) showed DNA aneuploidy; 20 of these had been previously treated with chemotherapy or radiotherapy, or both. DNA aneuploidy was seen as hyperdiploidy in all cases except one, and it varied from slightly hyperdiploid to tetraploid. The incidence of aneuploidy increased significantly with increasing histological grade (p = 0.0002) and was not related to previous treatment. The low, intermediate, and high grade lymphomas had 14% (six of 43), 47% (27 of 58), and 62.5% (five of eight) cases, respectively, that showed DNA aneuploidy. The percentage of cells in S phase increased significantly with a higher histological grade (p less than 0.0001). The median S fraction in the low, intermediate, and high grade lymphomas was 1.0 (0.5 to 10)% 4 (0.4 to 35)%, and 27 (4.6-56)%, respectively. There is a significant correlation between histological grade and S fraction and the presence or absence of aneuploidy. There is heterogeneity, however, within both histological grade and a histological subtype.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and Association of Clinical Pathologists</pub><pmid>3760241</pmid><doi>10.1136/jcp.39.9.987</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aneuploidy Biological and medical sciences DNA, Neoplasm - genetics Flow Cytometry Hematologic and hematopoietic diseases Humans Interphase Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Lymphoma - ultrastructure Medical sciences |
title | DNA ploidy patterns and cytokinetics of non-Hodgkin's lymphoma |
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