Nyla A. Heerema , John C. Byrd , Paola S. Dal Cin , Marie L. Dell’ Aquila , Prasad R.K. Koduru , Ayala Aviram , Stephanie A. Smoley , Laura Z. Rassenti , Andrew W. Greaves , Jennifer R. Brown , Kanti R. Rai , Thomas J. Kipps , Neil E. Kay , Daniel L. Van Dyke , Chronic Lymphocytic Leukemia Research Consortium
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More clonal abnormalities were observed after culture of CLL cells with CpG-ODN than with the traditional pokeweed mitogen plus 12-<em>O</em>-tetradecanoylphorbol-13-acetate (PWM+TPA). All clonal abnormalities in PWM+TPA cultures were observed in CpG-ODN cultures, whereas CpG-ODN identified some clones not found by PWM+TPA. CpG-ODN stimulation of one normal control sample and 12 CLL samples showed that, excepting clones of del(13q) in low frequencies and one translocation, results in all five laboratories were consistent, and all abnormalities were concordant with FISH. Abnormal clones in CLL were more readily detected with CpG-ODN stimulation than with traditional B-cell mitogens. With CpG-ODN stimulation, abnormalities were reproducible among cytogenetic laboratories. CpG-ODN did not appear to induce aberrations in cell culture, but did enhance detection of abnormalities and complexity in CLL. Because karyotypic complexity is prognostic and is not detectable by standard FISH analyses, stimulation with CpG-ODN is useful for identifying this additional prognostic factor in CLL.</p></div>","PeriodicalId":55596,"journal":{"name":"Cancer Genetics and Cytogenetics","volume":"203 2","pages":"Pages 134-140"},"PeriodicalIF":0.0000,"publicationDate":"2010-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.cancergencyto.2010.07.128","citationCount":"50","resultStr":"{\"title\":\"Stimulation of chronic lymphocytic leukemia cells with CpG oligodeoxynucleotide gives consistent karyotypic results among laboratories: a CLL Research Consortium (CRC) Study\",\"authors\":\"Nyla A. Heerema , John C. Byrd , Paola S. Dal Cin , Marie L. Dell’ Aquila , Prasad R.K. Koduru , Ayala Aviram , Stephanie A. Smoley , Laura Z. Rassenti , Andrew W. Greaves , Jennifer R. Brown , Kanti R. Rai , Thomas J. Kipps , Neil E. 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引用次数: 50
摘要
细胞遗传学异常是慢性淋巴细胞白血病的重要预后指标。历史上,只有间期细胞遗传学在CLL临床有用,因为传统的有丝分裂原不是有效的有丝分裂刺激剂。最近,CpG-oligodeoxynucleotide (ODN)刺激在CLL细胞中显示出有效性。CLL研究联盟通过五个实验室测试了CpG-ODN刺激检测染色体异常克隆的有效性和可重复性。用CpG-ODN培养CLL细胞后,观察到的克隆异常比用传统的美洲商田有丝分裂原加12- o - tetradecanoylphorol -13-acetate (PWM+TPA)培养CLL细胞多。在PWM+TPA培养中,所有克隆异常都在CpG-ODN培养中观察到,而CpG-ODN培养中发现了一些PWM+TPA未发现的克隆。1个正常对照样本和12个CLL样本的CpG-ODN刺激结果显示,除del(13q)克隆频率较低和1个易位外,5个实验室的结果一致,所有异常均与FISH一致。与传统的b细胞有丝分裂原相比,CpG-ODN刺激更容易检测到CLL中的异常克隆。在CpG-ODN刺激下,异常在细胞遗传学实验室中是可重复的。CpG-ODN在细胞培养中没有出现畸变,但确实增强了对CLL异常和复杂性的检测。由于核型复杂性是一种预后因素,不能通过标准的FISH分析检测到,因此CpG-ODN刺激有助于识别CLL中这一额外的预后因素。
Stimulation of chronic lymphocytic leukemia cells with CpG oligodeoxynucleotide gives consistent karyotypic results among laboratories: a CLL Research Consortium (CRC) Study
Cytogenetic abnormalities are important prognostic indicators in CLL. Historically, only interphase cytogenetics was clinically useful in CLL, because traditional mitogens are not effective mitotic stimulants. Recently, CpG-oligodeoxynucleotide (ODN) stimulation has shown effectiveness in CLL cells. The CLL Research Consortium tested the effectiveness and reproducibility of CpG-ODN stimulation for detecting chromosomally abnormal clones by five laboratories. More clonal abnormalities were observed after culture of CLL cells with CpG-ODN than with the traditional pokeweed mitogen plus 12-O-tetradecanoylphorbol-13-acetate (PWM+TPA). All clonal abnormalities in PWM+TPA cultures were observed in CpG-ODN cultures, whereas CpG-ODN identified some clones not found by PWM+TPA. CpG-ODN stimulation of one normal control sample and 12 CLL samples showed that, excepting clones of del(13q) in low frequencies and one translocation, results in all five laboratories were consistent, and all abnormalities were concordant with FISH. Abnormal clones in CLL were more readily detected with CpG-ODN stimulation than with traditional B-cell mitogens. With CpG-ODN stimulation, abnormalities were reproducible among cytogenetic laboratories. CpG-ODN did not appear to induce aberrations in cell culture, but did enhance detection of abnormalities and complexity in CLL. Because karyotypic complexity is prognostic and is not detectable by standard FISH analyses, stimulation with CpG-ODN is useful for identifying this additional prognostic factor in CLL.