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IKZF1 alterations and expression of CRLF2 predict prognosis in adult Chinese patients with B-cell precursor acute lymphoblastic leukemia
Acute Lymphoblastic Leukemia (ALL) is a common hematological malignancy in children, with a prognosis much worse in adults. The molecular characterization of ALL and its correlated prognostic significance are largely unknown. In this study, we analyzed the frequency of IKZF1 deletions, IK6 isoform,...
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Published in: | Leukemia & lymphoma 2017-01, Vol.58 (1), p.127-137 |
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container_title | Leukemia & lymphoma |
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creator | Fang, Qiuyun Zhao, Xingli Li, Qinghua Li, Yan Liu, Kaiqi Tang, Kejing Wang, Ying Liu, Bingcheng Wang, Min Xing, Haiyan Rao, Qing Tian, Zheng Wang, Jianxiang Mi, Yingchang |
description | Acute Lymphoblastic Leukemia (ALL) is a common hematological malignancy in children, with a prognosis much worse in adults. The molecular characterization of ALL and its correlated prognostic significance are largely unknown. In this study, we analyzed the frequency of IKZF1 deletions, IK6 isoform, and CRLF2 overexpression in 118 Chinese adult B-cell precursor ALL (B-ALL) patients to explore their associations with clinical prognosis. Our data showed that IKZF1 deletions and IK6 isoform were highly detected in adult patients, and both of them were related with worse prognosis in Ph
−
B-ALL, HR group of Ph
−
B-ALL, and/or B-ALL patients. Though the frequency of CRLF2 overexpression was similar to children, it had an independent prognostic significance for standard-risk and Ph
−
adult patients. Our study provided insights into the prognostic significance of certain genetic features in B-ALL patients. Further therapeutic strategies targeting these abnormalities potentially improving the prognosis of B-ALL are warranted. |
doi_str_mv | 10.1080/10428194.2016.1180682 |
format | article |
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−
B-ALL, HR group of Ph
−
B-ALL, and/or B-ALL patients. Though the frequency of CRLF2 overexpression was similar to children, it had an independent prognostic significance for standard-risk and Ph
−
adult patients. Our study provided insights into the prognostic significance of certain genetic features in B-ALL patients. Further therapeutic strategies targeting these abnormalities potentially improving the prognosis of B-ALL are warranted.</description><identifier>ISSN: 1042-8194</identifier><identifier>EISSN: 1029-2403</identifier><identifier>DOI: 10.1080/10428194.2016.1180682</identifier><identifier>PMID: 27157479</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>Acute Lymphoblastic Leukemia ; Adolescent ; Adult ; Alternative Splicing ; Biomarkers, Tumor ; CRLF2 ; Female ; Gene Deletion ; Gene Expression ; Gene Frequency ; Genetic Variation ; Humans ; IK6 ; Ikaros Transcription Factor - genetics ; IKZF1 ; Male ; Middle Aged ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality ; Prognosis ; Receptors, Cytokine - genetics ; Survival Analysis ; Young Adult</subject><ispartof>Leukemia & lymphoma, 2017-01, Vol.58 (1), p.127-137</ispartof><rights>2016 Informa UK Limited, trading as Taylor & Francis Group 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c366t-7cab77ddd8054d7ee9c830a70e5f8705ea49788e9f2a8fcc0273df9b541b98a83</citedby><cites>FETCH-LOGICAL-c366t-7cab77ddd8054d7ee9c830a70e5f8705ea49788e9f2a8fcc0273df9b541b98a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27157479$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fang, Qiuyun</creatorcontrib><creatorcontrib>Zhao, Xingli</creatorcontrib><creatorcontrib>Li, Qinghua</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><creatorcontrib>Liu, Kaiqi</creatorcontrib><creatorcontrib>Tang, Kejing</creatorcontrib><creatorcontrib>Wang, Ying</creatorcontrib><creatorcontrib>Liu, Bingcheng</creatorcontrib><creatorcontrib>Wang, Min</creatorcontrib><creatorcontrib>Xing, Haiyan</creatorcontrib><creatorcontrib>Rao, Qing</creatorcontrib><creatorcontrib>Tian, Zheng</creatorcontrib><creatorcontrib>Wang, Jianxiang</creatorcontrib><creatorcontrib>Mi, Yingchang</creatorcontrib><title>IKZF1 alterations and expression of CRLF2 predict prognosis in adult Chinese patients with B-cell precursor acute lymphoblastic leukemia</title><title>Leukemia & lymphoma</title><addtitle>Leuk Lymphoma</addtitle><description>Acute Lymphoblastic Leukemia (ALL) is a common hematological malignancy in children, with a prognosis much worse in adults. The molecular characterization of ALL and its correlated prognostic significance are largely unknown. In this study, we analyzed the frequency of IKZF1 deletions, IK6 isoform, and CRLF2 overexpression in 118 Chinese adult B-cell precursor ALL (B-ALL) patients to explore their associations with clinical prognosis. Our data showed that IKZF1 deletions and IK6 isoform were highly detected in adult patients, and both of them were related with worse prognosis in Ph
−
B-ALL, HR group of Ph
−
B-ALL, and/or B-ALL patients. Though the frequency of CRLF2 overexpression was similar to children, it had an independent prognostic significance for standard-risk and Ph
−
adult patients. Our study provided insights into the prognostic significance of certain genetic features in B-ALL patients. Further therapeutic strategies targeting these abnormalities potentially improving the prognosis of B-ALL are warranted.</description><subject>Acute Lymphoblastic Leukemia</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Alternative Splicing</subject><subject>Biomarkers, Tumor</subject><subject>CRLF2</subject><subject>Female</subject><subject>Gene Deletion</subject><subject>Gene Expression</subject><subject>Gene Frequency</subject><subject>Genetic Variation</subject><subject>Humans</subject><subject>IK6</subject><subject>Ikaros Transcription Factor - genetics</subject><subject>IKZF1</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality</subject><subject>Prognosis</subject><subject>Receptors, Cytokine - genetics</subject><subject>Survival Analysis</subject><subject>Young Adult</subject><issn>1042-8194</issn><issn>1029-2403</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kcGOFCEQhjtG466rj6Dh6KVHoOkGburE0Y2TmBi9eCE0FA5Kwwh01nkDH9vuzKxHTwWV76-_4G-a5wRvCBb4FcGMCiLZhmIybAgReBD0QXNNMJUtZbh7uJ4ZbVfoqnlSyg-McS8H-ri5opz0nHF53fy5_fhtR5AOFbKuPsWCdLQIfh8zlLLcUXJo-3m_o2jpWG_qUtP3mIovyEek7Rwq2h58hALouIyAWAu68_WA3rYGQlh1Zs4lZaTNXAGF03Q8pDHoUr1BAeafMHn9tHnkdCjw7FJvmq-7d1-2H9r9p_e32zf71nTDUFtu9Mi5tVbgnlkOII3osOYYeic47kEzyYUA6agWzhhMeWedHHtGRim06G6al-e5yzN-zVCqmnxZ99QR0lwUEXQYuGS0X9D-jJqcSsng1DH7SeeTIlitIaj7ENQagrqEsOheXCzmcQL7T3X_6wvw-gz46FKe9F3KwaqqTyFll3U0vqju_x5_AUcHmGg</recordid><startdate>20170102</startdate><enddate>20170102</enddate><creator>Fang, Qiuyun</creator><creator>Zhao, Xingli</creator><creator>Li, Qinghua</creator><creator>Li, Yan</creator><creator>Liu, Kaiqi</creator><creator>Tang, Kejing</creator><creator>Wang, Ying</creator><creator>Liu, Bingcheng</creator><creator>Wang, Min</creator><creator>Xing, Haiyan</creator><creator>Rao, Qing</creator><creator>Tian, Zheng</creator><creator>Wang, Jianxiang</creator><creator>Mi, Yingchang</creator><general>Taylor & Francis</general><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>7X8</scope></search><sort><creationdate>20170102</creationdate><title>IKZF1 alterations and expression of CRLF2 predict prognosis in adult Chinese patients with B-cell precursor acute lymphoblastic leukemia</title><author>Fang, Qiuyun ; Zhao, Xingli ; Li, Qinghua ; Li, Yan ; Liu, Kaiqi ; Tang, Kejing ; Wang, Ying ; Liu, Bingcheng ; Wang, Min ; Xing, Haiyan ; Rao, Qing ; Tian, Zheng ; Wang, Jianxiang ; Mi, Yingchang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c366t-7cab77ddd8054d7ee9c830a70e5f8705ea49788e9f2a8fcc0273df9b541b98a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acute Lymphoblastic Leukemia</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Alternative Splicing</topic><topic>Biomarkers, Tumor</topic><topic>CRLF2</topic><topic>Female</topic><topic>Gene Deletion</topic><topic>Gene Expression</topic><topic>Gene Frequency</topic><topic>Genetic Variation</topic><topic>Humans</topic><topic>IK6</topic><topic>Ikaros Transcription Factor - genetics</topic><topic>IKZF1</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality</topic><topic>Prognosis</topic><topic>Receptors, Cytokine - genetics</topic><topic>Survival Analysis</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fang, Qiuyun</creatorcontrib><creatorcontrib>Zhao, Xingli</creatorcontrib><creatorcontrib>Li, Qinghua</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><creatorcontrib>Liu, Kaiqi</creatorcontrib><creatorcontrib>Tang, Kejing</creatorcontrib><creatorcontrib>Wang, Ying</creatorcontrib><creatorcontrib>Liu, Bingcheng</creatorcontrib><creatorcontrib>Wang, Min</creatorcontrib><creatorcontrib>Xing, Haiyan</creatorcontrib><creatorcontrib>Rao, Qing</creatorcontrib><creatorcontrib>Tian, Zheng</creatorcontrib><creatorcontrib>Wang, Jianxiang</creatorcontrib><creatorcontrib>Mi, Yingchang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Leukemia & lymphoma</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fang, Qiuyun</au><au>Zhao, Xingli</au><au>Li, Qinghua</au><au>Li, Yan</au><au>Liu, Kaiqi</au><au>Tang, Kejing</au><au>Wang, Ying</au><au>Liu, Bingcheng</au><au>Wang, Min</au><au>Xing, Haiyan</au><au>Rao, Qing</au><au>Tian, Zheng</au><au>Wang, Jianxiang</au><au>Mi, Yingchang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>IKZF1 alterations and expression of CRLF2 predict prognosis in adult Chinese patients with B-cell precursor acute lymphoblastic leukemia</atitle><jtitle>Leukemia & lymphoma</jtitle><addtitle>Leuk Lymphoma</addtitle><date>2017-01-02</date><risdate>2017</risdate><volume>58</volume><issue>1</issue><spage>127</spage><epage>137</epage><pages>127-137</pages><issn>1042-8194</issn><eissn>1029-2403</eissn><abstract>Acute Lymphoblastic Leukemia (ALL) is a common hematological malignancy in children, with a prognosis much worse in adults. The molecular characterization of ALL and its correlated prognostic significance are largely unknown. In this study, we analyzed the frequency of IKZF1 deletions, IK6 isoform, and CRLF2 overexpression in 118 Chinese adult B-cell precursor ALL (B-ALL) patients to explore their associations with clinical prognosis. Our data showed that IKZF1 deletions and IK6 isoform were highly detected in adult patients, and both of them were related with worse prognosis in Ph
−
B-ALL, HR group of Ph
−
B-ALL, and/or B-ALL patients. Though the frequency of CRLF2 overexpression was similar to children, it had an independent prognostic significance for standard-risk and Ph
−
adult patients. Our study provided insights into the prognostic significance of certain genetic features in B-ALL patients. Further therapeutic strategies targeting these abnormalities potentially improving the prognosis of B-ALL are warranted.</abstract><cop>United States</cop><pub>Taylor & Francis</pub><pmid>27157479</pmid><doi>10.1080/10428194.2016.1180682</doi><tpages>11</tpages></addata></record> |
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subjects | Acute Lymphoblastic Leukemia Adolescent Adult Alternative Splicing Biomarkers, Tumor CRLF2 Female Gene Deletion Gene Expression Gene Frequency Genetic Variation Humans IK6 Ikaros Transcription Factor - genetics IKZF1 Male Middle Aged Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality Prognosis Receptors, Cytokine - genetics Survival Analysis Young Adult |
title | IKZF1 alterations and expression of CRLF2 predict prognosis in adult Chinese patients with B-cell precursor acute lymphoblastic leukemia |
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