Zeta-associated protein 70 expression in chronic lymphocytic leukemia: Relevance in Indian context
Background: Chronic lymphocytic leukemia (CLL) is prognosticated using the Rai and the Binet's staging. In the past few years, new parameters have been considered for prognostication. One such marker that has been a subject of speculation and found useful by some western studies is zeta-associa...
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description | Background: Chronic lymphocytic leukemia (CLL) is prognosticated using the Rai and the Binet's staging. In the past few years, new parameters have been considered for prognostication. One such marker that has been a subject of speculation and found useful by some western studies is zeta-associated protein 70 (ZAP-70). Aim: To investigate the prevalence of ZAP-70 and find out its association with other prognostic markers like Rai and Binet's stage and CD38 in Indian CLL patients. Materials and Methods: Twenty-nine newly diagnosed cases of CLL were selected over 1 year. Immunophenotyping was done and expression of CD38 and ZAP-70 was evaluated on gated CLL cells. Statistical Analysis: Qualitative data were expressed as frequency and percentage. Differences between groups were evaluated using Student's t-test for quantitative data and Chi-square test/Fisher's exact t-test for qualitative variables. A P value less than 0.05 was considered significant. Results and Conclusion: We found a lower prevalence rate of ZAP-70 (2/29, 6.89%) with no association with any of the conventional poor prognostic factors. A large number of our CLL patients fall into the good prognostic group (22/29, ZAP 70−/CD38−) with a least number in the poor prognostic group (2/29, ZAP-70 + CD38+). Also, no association was found between ZAP-70 and CD38. The findings of the present study suggest that the majority of CLL patients in India have a good prognosis, may not require treatment, and have good overall survival. Geographical variations, genetic makeup, and natural history of the CLL could be the cause of such differences from western literature. |
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In the past few years, new parameters have been considered for prognostication. One such marker that has been a subject of speculation and found useful by some western studies is zeta-associated protein 70 (ZAP-70). Aim: To investigate the prevalence of ZAP-70 and find out its association with other prognostic markers like Rai and Binet's stage and CD38 in Indian CLL patients. Materials and Methods: Twenty-nine newly diagnosed cases of CLL were selected over 1 year. Immunophenotyping was done and expression of CD38 and ZAP-70 was evaluated on gated CLL cells. Statistical Analysis: Qualitative data were expressed as frequency and percentage. Differences between groups were evaluated using Student's t-test for quantitative data and Chi-square test/Fisher's exact t-test for qualitative variables. A P value less than 0.05 was considered significant. Results and Conclusion: We found a lower prevalence rate of ZAP-70 (2/29, 6.89%) with no association with any of the conventional poor prognostic factors. A large number of our CLL patients fall into the good prognostic group (22/29, ZAP 70−/CD38−) with a least number in the poor prognostic group (2/29, ZAP-70 + CD38+). Also, no association was found between ZAP-70 and CD38. The findings of the present study suggest that the majority of CLL patients in India have a good prognosis, may not require treatment, and have good overall survival. Geographical variations, genetic makeup, and natural history of the CLL could be the cause of such differences from western literature.</description><identifier>ISSN: 0377-4929</identifier><identifier>EISSN: 0974-5130</identifier><identifier>DOI: 10.4103/IJPM.IJPM_1200_20</identifier><identifier>PMID: 37077070</identifier><language>eng</language><publisher>India: Wolters Kluwer India Pvt. Ltd</publisher><subject>ADP-ribosyl Cyclase 1 - genetics ; ADP-ribosyl Cyclase 1 - metabolism ; CD38 antigen ; Chi-square test ; Chronic lymphocytic leukemia ; Development and progression ; Genetic diversity ; Geographical variations ; Humans ; India - epidemiology ; Leukemia ; Leukemia, Lymphocytic, Chronic, B-Cell - diagnosis ; Medical prognosis ; Prognosis ; Proteins ; Qualitative analysis ; Statistical analysis ; ZAP-70 protein ; ZAP-70 Protein-Tyrosine Kinase - genetics ; ZAP-70 Protein-Tyrosine Kinase - metabolism</subject><ispartof>Indian journal of pathology & microbiology, 2023-04, Vol.66 (2), p.291-294</ispartof><rights>COPYRIGHT 2023 Medknow Publications and Media Pvt. Ltd.</rights><rights>2023. This article is published under (http://creativecommons.org/licenses/by-nc-sa/3.0/) (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c413t-98256206c73409d418ef066521c5dbb519b35c75ba8f6bc26f11e2bd2a0a66d63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37077070$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gupta, Richa</creatorcontrib><creatorcontrib>Garg, Neha</creatorcontrib><creatorcontrib>Singh, Abha</creatorcontrib><creatorcontrib>Jain, Shyam</creatorcontrib><title>Zeta-associated protein 70 expression in chronic lymphocytic leukemia: Relevance in Indian context</title><title>Indian journal of pathology & microbiology</title><addtitle>Indian J Pathol Microbiol</addtitle><description>Background: Chronic lymphocytic leukemia (CLL) is prognosticated using the Rai and the Binet's staging. In the past few years, new parameters have been considered for prognostication. One such marker that has been a subject of speculation and found useful by some western studies is zeta-associated protein 70 (ZAP-70). Aim: To investigate the prevalence of ZAP-70 and find out its association with other prognostic markers like Rai and Binet's stage and CD38 in Indian CLL patients. Materials and Methods: Twenty-nine newly diagnosed cases of CLL were selected over 1 year. Immunophenotyping was done and expression of CD38 and ZAP-70 was evaluated on gated CLL cells. Statistical Analysis: Qualitative data were expressed as frequency and percentage. Differences between groups were evaluated using Student's t-test for quantitative data and Chi-square test/Fisher's exact t-test for qualitative variables. A P value less than 0.05 was considered significant. Results and Conclusion: We found a lower prevalence rate of ZAP-70 (2/29, 6.89%) with no association with any of the conventional poor prognostic factors. A large number of our CLL patients fall into the good prognostic group (22/29, ZAP 70−/CD38−) with a least number in the poor prognostic group (2/29, ZAP-70 + CD38+). Also, no association was found between ZAP-70 and CD38. The findings of the present study suggest that the majority of CLL patients in India have a good prognosis, may not require treatment, and have good overall survival. Geographical variations, genetic makeup, and natural history of the CLL could be the cause of such differences from western literature.</description><subject>ADP-ribosyl Cyclase 1 - genetics</subject><subject>ADP-ribosyl Cyclase 1 - metabolism</subject><subject>CD38 antigen</subject><subject>Chi-square test</subject><subject>Chronic lymphocytic leukemia</subject><subject>Development and progression</subject><subject>Genetic diversity</subject><subject>Geographical variations</subject><subject>Humans</subject><subject>India - epidemiology</subject><subject>Leukemia</subject><subject>Leukemia, Lymphocytic, Chronic, B-Cell - diagnosis</subject><subject>Medical prognosis</subject><subject>Prognosis</subject><subject>Proteins</subject><subject>Qualitative analysis</subject><subject>Statistical analysis</subject><subject>ZAP-70 protein</subject><subject>ZAP-70 Protein-Tyrosine Kinase - genetics</subject><subject>ZAP-70 Protein-Tyrosine Kinase - metabolism</subject><issn>0377-4929</issn><issn>0974-5130</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kk1v1DAQhi0EoqXwA7igSFy4ZPFHbMfcqgrooiIQggsXy3Em1N3EXmyH7f57HLZ8FIFs2aPR847G8xqhxwSvGoLZ8_Wb929Xy6EJxVhTfAcdYyWbmhOG75aYSVk3iqoj9CClK4xFQzm7j46YxLJsfIy6z5BNbVIK1pkMfbWNIYPzlcQVXG8jpOSCr0rCXsbgna3G_bS9DHaflxjmDUzOvKg-wAjfjLewoGvfO1MUwWe4zg_RvcGMCR7d3Cfo06uXH8_O64t3r9dnpxe1bQjLtWopFxQLK1mDVd-QFgYsBKfE8r7rOFEd41byzrSD6CwVAyFAu54abIToBTtBzw51yxO-zpCynlyyMI7GQ5iTpi1mSjDWqoI-_Qu9CnP0pbuFUoxyzpvf1BczgnZ-CDkauxTVp7JpGZMc00Kt_kGV1ZfJlBHA4Er-loAcBDaGlCIMehvdZOJeE6wXX_UPS__0tWie3DQ8dxP0vxQ_jSzA-QHYhTFDTJtx3kHUhd34sPt_ZU0V0bf-APsO5bK1Tw</recordid><startdate>20230401</startdate><enddate>20230401</enddate><creator>Gupta, Richa</creator><creator>Garg, Neha</creator><creator>Singh, Abha</creator><creator>Jain, Shyam</creator><general>Wolters Kluwer India Pvt. 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genetics</topic><topic>ADP-ribosyl Cyclase 1 - metabolism</topic><topic>CD38 antigen</topic><topic>Chi-square test</topic><topic>Chronic lymphocytic leukemia</topic><topic>Development and progression</topic><topic>Genetic diversity</topic><topic>Geographical variations</topic><topic>Humans</topic><topic>India - epidemiology</topic><topic>Leukemia</topic><topic>Leukemia, Lymphocytic, Chronic, B-Cell - diagnosis</topic><topic>Medical prognosis</topic><topic>Prognosis</topic><topic>Proteins</topic><topic>Qualitative analysis</topic><topic>Statistical analysis</topic><topic>ZAP-70 protein</topic><topic>ZAP-70 Protein-Tyrosine Kinase - genetics</topic><topic>ZAP-70 Protein-Tyrosine Kinase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gupta, Richa</creatorcontrib><creatorcontrib>Garg, Neha</creatorcontrib><creatorcontrib>Singh, Abha</creatorcontrib><creatorcontrib>Jain, Shyam</creatorcontrib><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>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Technology Research 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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</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>MEDLINE - Academic</collection><jtitle>Indian journal of pathology & microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gupta, Richa</au><au>Garg, Neha</au><au>Singh, Abha</au><au>Jain, Shyam</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Zeta-associated protein 70 expression in chronic lymphocytic leukemia: Relevance in Indian context</atitle><jtitle>Indian journal of pathology & microbiology</jtitle><addtitle>Indian J Pathol Microbiol</addtitle><date>2023-04-01</date><risdate>2023</risdate><volume>66</volume><issue>2</issue><spage>291</spage><epage>294</epage><pages>291-294</pages><issn>0377-4929</issn><eissn>0974-5130</eissn><abstract>Background: Chronic lymphocytic leukemia (CLL) is prognosticated using the Rai and the Binet's staging. In the past few years, new parameters have been considered for prognostication. One such marker that has been a subject of speculation and found useful by some western studies is zeta-associated protein 70 (ZAP-70). Aim: To investigate the prevalence of ZAP-70 and find out its association with other prognostic markers like Rai and Binet's stage and CD38 in Indian CLL patients. Materials and Methods: Twenty-nine newly diagnosed cases of CLL were selected over 1 year. Immunophenotyping was done and expression of CD38 and ZAP-70 was evaluated on gated CLL cells. Statistical Analysis: Qualitative data were expressed as frequency and percentage. Differences between groups were evaluated using Student's t-test for quantitative data and Chi-square test/Fisher's exact t-test for qualitative variables. A P value less than 0.05 was considered significant. Results and Conclusion: We found a lower prevalence rate of ZAP-70 (2/29, 6.89%) with no association with any of the conventional poor prognostic factors. A large number of our CLL patients fall into the good prognostic group (22/29, ZAP 70−/CD38−) with a least number in the poor prognostic group (2/29, ZAP-70 + CD38+). Also, no association was found between ZAP-70 and CD38. The findings of the present study suggest that the majority of CLL patients in India have a good prognosis, may not require treatment, and have good overall survival. Geographical variations, genetic makeup, and natural history of the CLL could be the cause of such differences from western literature.</abstract><cop>India</cop><pub>Wolters Kluwer India Pvt. Ltd</pub><pmid>37077070</pmid><doi>10.4103/IJPM.IJPM_1200_20</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | ADP-ribosyl Cyclase 1 - genetics ADP-ribosyl Cyclase 1 - metabolism CD38 antigen Chi-square test Chronic lymphocytic leukemia Development and progression Genetic diversity Geographical variations Humans India - epidemiology Leukemia Leukemia, Lymphocytic, Chronic, B-Cell - diagnosis Medical prognosis Prognosis Proteins Qualitative analysis Statistical analysis ZAP-70 protein ZAP-70 Protein-Tyrosine Kinase - genetics ZAP-70 Protein-Tyrosine Kinase - metabolism |
title | Zeta-associated protein 70 expression in chronic lymphocytic leukemia: Relevance in Indian context |
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