CAT rs1001179 Single Nucleotide Polymorphism Identifies an Aggressive Clinical Behavior in Chronic Lymphocytic Leukemia

IF 3.3 4区 医学 Q2 HEMATOLOGY
Marilisa Galasso, Vittoria Salaorni, Riccardo Moia, Valentina Mozzo, Ester Lovato, Chiara Cosentino, Omar Perbellini, Simona Gambino, Ornella Lovato, Maria Elena Carazzolo, Isacco Ferrarini, Francesca M. Quaglia, Massimo Donadelli, Maria G. Romanelli, Carlo Visco, Mauro Krampera, Gianluca Gaidano, Maria T. Scupoli
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Abstract

Chronic lymphocytic leukemia (CLL) is characterized by an extremely variable clinical course. Although several parameters have been shown to be associated with clinical outcomes in patients with CLL, there remains substantial intragroup clinical heterogeneity in otherwise molecularly and staging homogeneous CLL subgroups. We have recently shown that high catalase (CAT) expression identifies patients with an aggressive clinical course and that higher CAT expression is associated with the presence of the rs1001179 single nucleotide polymorphism (SNP) T allele in the CAT promoter. Herein, we genotyped CLL patients for CAT rs1001179 SNP in an exploratory study (n = 235) and in a sequential independent validation study (n = 531). Time-to-event modeling analyses for time-to-first-treatment (TTFT) from the two patients' cohorts showed that TT genotype was associated with a shorter TTFT, independently of other currently used prognostic parameters in CLL. Moreover, the TT genotype identifies CLL patients with a faster clinical progression even within subgroups of patients with low-risk biological and clinical hallmarks. In conclusion, our data show that the TT genotype identifies CLL patients with a shorter TTFT, pointing to this SNP as a possible prognostic factor, which can improve patients' risk stratification leading to better patient management and personalized therapeutic choices.

CAT rs1001179 单核苷酸多态性可识别慢性淋巴细胞白血病的侵袭性临床表现
慢性淋巴细胞白血病(CLL)的临床病程变化极大。虽然有几项参数已被证明与 CLL 患者的临床预后有关,但在分子和分期均一的 CLL 亚组中,组内临床异质性仍然很大。我们最近发现,过氧化氢酶(CAT)的高表达可识别临床病程具有侵袭性的患者,而CAT的高表达与CAT启动子中存在rs1001179单核苷酸多态性(SNP)T等位基因有关。在此,我们在一项探索性研究(n = 235)和一项连续的独立验证研究(n = 531)中对CLL患者进行了CAT rs1001179 SNP基因分型。对这两个患者队列的首次治疗时间(TTFT)进行的时间到事件模型分析表明,TT 基因型与较短的 TTFT 相关,与 CLL 目前使用的其他预后参数无关。此外,即使在具有低风险生物和临床特征的患者亚群中,TT 基因型也能识别临床进展较快的 CLL 患者。总之,我们的数据显示,TT 基因型能识别出 TTFT 较短的 CLL 患者,这表明该 SNP 可能是一个预后因素,它能改善患者的风险分层,从而改善患者管理和个性化治疗选择。
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来源期刊
Hematological Oncology
Hematological Oncology 医学-血液学
CiteScore
4.20
自引率
6.10%
发文量
147
审稿时长
>12 weeks
期刊介绍: Hematological Oncology considers for publication articles dealing with experimental and clinical aspects of neoplastic diseases of the hemopoietic and lymphoid systems and relevant related matters. Translational studies applying basic science to clinical issues are particularly welcomed. Manuscripts dealing with the following areas are encouraged: -Clinical practice and management of hematological neoplasia, including: acute and chronic leukemias, malignant lymphomas, myeloproliferative disorders -Diagnostic investigations, including imaging and laboratory assays -Epidemiology, pathology and pathobiology of hematological neoplasia of hematological diseases -Therapeutic issues including Phase 1, 2 or 3 trials as well as allogeneic and autologous stem cell transplantation studies -Aspects of the cell biology, molecular biology, molecular genetics and cytogenetics of normal or diseased hematopoeisis and lymphopoiesis, including stem cells and cytokines and other regulatory systems. Concise, topical review material is welcomed, especially if it makes new concepts and ideas accessible to a wider community. Proposals for review material may be discussed with the Editor-in-Chief. Collections of case material and case reports will be considered only if they have broader scientific or clinical relevance.
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