EKLF (KLF1): A Potential Tumor Suppressor?
EKLF (KLF1):潜在的肿瘤抑制剂?
基本信息
- 批准号:8102179
- 负责人:
- 金额:$ 17.88万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2010
- 资助国家:美国
- 起止时间:2010-07-01 至 2013-06-30
- 项目状态:已结题
- 来源:
- 关键词:Acute Myelocytic LeukemiaAddressAntibodiesAttenuatedBiological MarkersBone MarrowBone Marrow CellsCell CycleCell LineCell ProliferationCellsCharacteristicsErythroidEvaluationFamily memberFutureGeneticGenetic TranscriptionGrantHematopoiesisHematopoieticHematopoietic NeoplasmsHigh Pressure Liquid ChromatographyHumanLeadLeukemic CellMalignant - descriptorMalignant NeoplasmsMegakaryocytopoiesesModificationMolecularMutateNaturePatientsPlayPropertyProteinsReagentRepressionRoleSamplingSeriesTestingTimeTimeLineTissuesTumor Suppressor ProteinsVariantZinc Fingersbasecancer cellclinically relevantdesignerythroid Kruppel-like factorinhibitor/antagonistleukemialeukemogenesismutantnovelpreventpublic health relevanceresearch studytranscription factor
项目摘要
DESCRIPTION (provided by applicant): Functional inactivation of tumor suppressors plays an important role in malignancy. Many tumor suppressors normally interface with the cell cycle machinery and form part of its exquisite control mechanism. Loss of these controls can lead to unrestricted proliferation and impaired differentiation, both of which are characteristic of acute myeloid leukemia. EKLF (Erythroid Kr¿ppel Like Factor; KLF1) is a zinc finger hematopoietic transcription factor that is absolutely critical for the erythroid lineage. Our recent studies have also revealed an unexpected role of EKLF as an inhibitor of megakaryopoiesis, suggesting a novel function of this transcription factor in lineage commitment during hematopoiesis. EKLF inhibits cellular proliferation and induces endogenous expression of the cell cycle inhibitor p21. As a result, we hypothesize that human EKLF may play a role in hematopoietic malignancy consistent with that of a tumor suppressor, and this exploratory proposal will evaluate this idea by two aims. In the first, we will use an antibody that recognizes human EKLF protein to analyze human normal and leukemic tissue and cell samples for the presence/absence of EKLF protein, and determine whether its expression correlates with a specific malignant subtype. In the second, the sequence of the complete human EKLF transcription unit will be compared between normal bone marrow and a number of human leukemic cell lines and malignant primary cells to see if EKLF is mutated in any of these lines. Functional tests of any variant EKLF proteins that are discovered will follow both of these aims and will also provide a basis for future experiments that extend beyond the timeline of this exploratory grant. Successful attainment of the aims in this proposal will determine whether mutated EKLF/KLF1 plays a role in leukemia, thus providing a novel biomarker, and will direct future applicability towards the most clinically relevant samples.
PUBLIC HEALTH RELEVANCE: Tumor suppressors play an important role in preventing malignancy. EKLF, a critical zinc finger hematopoietic transcription factor, has antiproliferative properties consistent with that of a tumor suppressor. As a result, our test hypothesis is that EKLF is playing an unappreciated role as a tumor suppressor, and that its dysregulation can contribute or lead to human leukemia.
描述(适用提供):肿瘤补充剂的功能失活在恶性肿瘤中起着重要作用。许多肿瘤补充剂通常与细胞周期机制接口,并构成其独家控制机制的一部分。这些对照的丧失会导致不受限制的增殖和分化受损,这两者都是急性髓样白血病的特征。 EKLF(红细胞类似于因子; KLF1)是锌指造血转录因子,对红细胞谱系绝对至关重要。我们最近的研究还揭示了EKLF作为巨核抑制剂的意外作用,这表明该转录因子在造血期间的谱系承诺中具有新的功能。 EKLF抑制细胞增殖并诱导细胞周期抑制剂p21的内源性表达。结果,我们假设人类EKLF可能在与肿瘤抑制剂一致的造血恶性肿瘤中发挥作用,并且该探险家将通过两个目标评估这一想法。首先,我们将使用一种识别人EKLF蛋白的抗体来分析人类正常和白血病组织以及细胞样品的存在/不存在EKLF蛋白,并确定其表达是否与特定的恶性亚型相关。在第二个中,将在正常骨髓和许多人类白血病细胞系和恶性原代细胞之间比较完整的人类EKLF转录单元的序列,以查看是否在任何这些线中都突变了EKLF。发现的任何变体EKLF蛋白的功能测试都将遵循这两个目标,还将为将来的实验提供基础,这些实验超出了探索性授予的时间表。在该提案中成功实现目标将确定突变的EKLF/KLF1是否在白血病中起作用,从而提供了一种新颖的生物标志物,并将将未来的适用性指向最临床相关的样本。
公共卫生相关性:肿瘤补充剂在预防恶性肿瘤中起着重要作用。 EKLF是一种临界锌指造血转录因子,具有与肿瘤抑制剂相一致的抗增殖特性。结果,我们的测试假设是EKLF作为肿瘤抑制剂的作用不欣赏,其功能障碍会导致或导致人类白血病。
项目成果
期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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JAMES J BIEKER其他文献
JAMES J BIEKER的其他文献
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{{ truncateString('JAMES J BIEKER', 18)}}的其他基金
Coordinate regulation of erythroid and macrophage lineages in development by EKLF/KLF1
EKLF/KLF1 对发育中红细胞和巨噬细胞谱系的协调调节
- 批准号:
10553699 - 财政年份:2020
- 资助金额:
$ 17.88万 - 项目类别:
Coordinate regulation of erythroid and macrophage lineages in development by EKLF/KLF1
EKLF/KLF1 对发育中红细胞和巨噬细胞谱系的协调调节
- 批准号:
10348762 - 财政年份:2020
- 资助金额:
$ 17.88万 - 项目类别:
Generation of cultured RBCs with rare phenotypes for transfusion from sources usually discarded during regular blood donations
产生具有罕见表型的培养红细胞,用于从定期献血期间通常丢弃的来源进行输血
- 批准号:
10188596 - 财政年份:2018
- 资助金额:
$ 17.88万 - 项目类别:
Generation of cultured RBCs with rare phenotypes for transfusion from sources usually discarded during regular blood donations
产生具有罕见表型的培养红细胞,用于从定期献血期间通常丢弃的来源进行输血
- 批准号:
9789365 - 财政年份:2018
- 资助金额:
$ 17.88万 - 项目类别:
Intrinsic and extrinsic control of erythropoietic maturation
红细胞生成成熟的内在和外在控制
- 批准号:
9042359 - 财政年份:2014
- 资助金额:
$ 17.88万 - 项目类别:
Intrinsic and extrinsic control of erythropoietic maturation
红细胞生成成熟的内在和外在控制
- 批准号:
9258426 - 财政年份:2014
- 资助金额:
$ 17.88万 - 项目类别:
Intrinsic and extrinsic control of erythropoietic maturation
红细胞生成成熟的内在和外在控制
- 批准号:
8714505 - 财政年份:2014
- 资助金额:
$ 17.88万 - 项目类别:
EKLF (KLF1): A Potential Tumor Suppressor?
EKLF (KLF1):潜在的肿瘤抑制剂?
- 批准号:
7901246 - 财政年份:2010
- 资助金额:
$ 17.88万 - 项目类别:
Redirecting hemoglobin expression during Human ES Cell differentiation
人胚胎干细胞分化过程中血红蛋白表达的重定向
- 批准号:
7814682 - 财政年份:2010
- 资助金额:
$ 17.88万 - 项目类别:
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