Cell Cycle Controlling Genes in Adult Acute Lymphoma

成人急性淋巴瘤的细胞周期控制基因

• 批准号: 6933884
• 负责人: GUILLERMO GARCIA-MANERO
• 金额: $ 13.59万
• 依托单位: UNIVERSITY OF TX MD ANDERSON CAN CTR
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-08-06 至 2007-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6933884
• 关键词: CpG islands; DNA methylation; acute lymphocytic leukemia; adult human (21+); bone marrow transplantation; cancer registry /resource; cancer risk; cell growth regulation; clinical research; data collection methodology /evaluation; gene expression; gene targeting; genetic markers; human subject; long term survivor; molecular pathology; neoplasm /cancer chemotherapy; neoplasm /cancer genetics; neoplasm /cancer relapse /recurrence; neoplastic process; nucleic acid sequence; polymerase chain reaction; prognosis; regulatory gene; statistics /biometry; therapy design /development

DESCRIPTION (provided by applicant): Adult acute lymphocytic leukemia (ALL) consists of a heterogeneous group of lymphoid malignancies. Treatment is stratified based on the presence of the Philadelphia chromosome (Ph), t(9;22) that occurs in 15% to 25% of patients. The rest of patients (Ph negative ALL) are routinely treated with intensive chemotherapy programs that do not discriminate against specific molecular characteristics. Although initial complete remission rates are in excess of 70%, long-term survival may vary from less than 5% for Ph positive to 35% for Ph negative patients. It is therefore of great importance to develop molecular tools to identify patients at high risk for relapse that may benefit from specific therapeutic interventions. Aberrant DNA methylation of promoter associated CpG islands is frequently observed in ALL. Genes involved directly or indirectly in cell cycle control appear to be particularly targeted in this disease, with methylation of p73, p15 or p57KIP2 occurring in 11% to 34% of patients. Preliminary data suggests that methylation of these genes identifies an ALL group at high risk for relapse that cannot otherwise be identified. Here, we propose the hypothesis that methylation of 2 or 3 genes of a pathway including p73, p15 and p57KIP2 identifies a subgroup of patients with ALL with poor prognosis. To test this hypothesis, we propose the following specific aim: to evaluate the methylation status of p73, p15 and p57KIP2 in a cohort of 300 patients with ALL homogeneously treated at our institution, and correlate this with survival. The sample size will provide enough power to allow for multivariate analysis. Analysis of DNA methylation will be performed using bisulfite PCR methods, and will be confirmed using bisulfite sequencing in selected cases. The implications of this project include the identification of a subgroup of patients with poor prognosis that may benefit from targeted therapies using hypomethylating agents and/or early allogeneic bone marrow transplantation in first complete remission.

描述（由申请方提供）：成人急性淋巴细胞白血病（ALL）由一组异质性淋巴恶性肿瘤组成。根据费城染色体（Ph）t（9;22）的存在对治疗进行分层，费城染色体在15%至25%的患者中发生。其余患者（Ph阴性ALL）常规接受强化化疗方案治疗，不区分特定分子特征。虽然初始完全缓解率超过70%，但长期生存率可能从Ph阳性患者的不到5%到Ph阴性患者的35%不等。因此，开发分子工具来识别可能受益于特定治疗干预的复发高风险患者非常重要。启动子相关CpG岛的异常DNA甲基化在ALL中常见。直接或间接参与细胞周期控制的基因似乎在这种疾病中特别有针对性，11%至34%的患者发生p73，p15或p57 KIP 2的甲基化。初步数据表明，这些基因的甲基化识别出了一个ALL组，该ALL组具有复发的高风险，而这是无法通过其他方式识别的。在这里，我们提出了一个假说，即甲基化的2或3个基因的通路，包括p73，p15和p57 KIP 2确定一个亚组的ALL患者预后不良。为了验证这一假设，我们提出了以下具体目标：评估在我们机构接受均匀治疗的300例ALL患者队列中p73、p15和p57 KIP 2的甲基化状态，并将其与生存率相关联。样本量将提供足够的把握度以进行多变量分析。将使用亚硫酸氢盐PCR方法进行DNA甲基化分析，并在选定病例中使用亚硫酸氢盐测序进行确认。该项目的意义包括确定一个亚组的预后不良的患者，可能受益于靶向治疗使用低甲基化剂和/或早期异基因骨髓移植在第一次完全缓解。

项目成果

Modifying the epigenome as a therapeutic strategy in myelodysplasia.

修改表观基因组作为骨髓增生异常的治疗策略。

• DOI: 10.1182/asheducation-2007.1.405
• 发表时间: 2007
• 期刊: Hematology. American Society of Hematology. Education Program
• 作者: Garcia-Manero,Guillermo

Residual DNA methylation at remission is prognostic in adult Philadelphia chromosome-negative acute lymphocytic leukemia.

• DOI: 10.1182/blood-2008-02-141002
• 发表时间: 2009-02
• 期刊: Blood
• 影响因子: 20.3
• 作者: Hui Yang;T. Kadia;Lianchun Xiao;C. Bueso-Ramos;K. Hoshino;D. Thomas;S. O'brien;E. Jabbour;S. Pierce;G. Rosner;H. Kantarjian;G. Garcia-Manero