Establishment of SCID mouse metastatic model of human malignant lymphoma and analysis of lectin binding properties on metastatic capacity

SCID小鼠人恶性淋巴瘤转移模型的建立及凝集素结合特性对转移能力的影响分析

基本信息

  • 批准号:
    07670209
  • 负责人:
  • 金额:
    $ 1.34万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 财政年份:
    1995
  • 资助国家:
    日本
  • 起止时间:
    1995 至 1996
  • 项目状态:
    已结题

项目摘要

1. Establishment of a metastatic SCID mouse model of human B-cell lymphoma lines :The human B-cell lymphoma lines (HBL-1, HBL-2, HBL-4, HBL-5, HBL-6, HBL-7, HBL-8, Daudi and Raji) were heterotransplanted subcutaneously into SCID mice. HBL-2, HBL-7 and HBL-8 cell lines showed a high spontaneous metastasis, whereas the other cell lines showed no or low-spontaneous metastasis. These high metastatic cell lines may be a useful tool to elucidate the metastatic mechanisms of human B-cell lymphoma.2. The relation between the binding sites for Glycine Max (SBA) lectin masked by sialylation and metastatic capacity in a SCID mouse model :A difference in cell surface carbohydrates between high-and no-or low-spontaneous metastatic human B-cell lymphoma lines were analyzed using lectin staining. The results showed that the masking of SBA lectin binding sites by sialic acid might be closely associated with metastatic capacity of human B-cell lymphoma lines in a SCID mouse model3. The relation between the lectin binding properties (VVA, ABA and PHA-L) and survival in 46 cases with human diffuse large B-cell lymphoma :The lectin binding properties on 46 cases with diffuse large B-cell lymphoma was analyzed in relation to survival. The lectin binding properties (VVA,ABA and PHA-L) were correlated with survival of patients with diffuse large B-cell lymphoma : The patients with lack or alterations of lectin binding sites of carbohydrates showed a worse prognosis in comparison to those without it.
1.人B细胞淋巴瘤细胞系SCID小鼠模型的建立:将人B细胞淋巴瘤细胞系HBL-1、HBL-2、HBL-4、HBL-5、HBL-6、HBL-7、HBL-8、Daudi和Raji移植到SCID小鼠皮下。HBL-2、HBL-7和HBL-8细胞系表现为高自发转移,而其他细胞系无自发转移或低自发转移。这些高转移细胞系可能是阐明人类B细胞淋巴瘤转移机制的有用工具。唾液酸化掩蔽的甘氨酸最大(SBA)凝集素结合位点与SCID小鼠模型转移能力的关系:用凝集素染色分析高转移性和无或低转移性B细胞淋巴瘤细胞表面碳水化合物的差异。结果表明,唾液酸对SBA凝集素结合部位的掩蔽可能与人B细胞淋巴瘤细胞系在SCID小鼠模型中的转移能力密切相关。46例弥漫性大B细胞淋巴瘤凝集素结合特性(VVA、ABA、PHA-L)与生存期的关系:分析46例弥漫性大B细胞淋巴瘤凝集素结合特性与生存期的关系。凝集素结合特性(VVA、ABA和PHA-L)与弥漫性大B细胞淋巴瘤患者的生存有关:糖类凝集素结合位点缺失或改变的患者预后较差。

项目成果

期刊论文数量(4)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Masafumi,Abe: "Analysis of lectin binding properties on human Burkitt's lymphoma cell lines that show high spontaneous metastasis to distant organs in SCID mice:The binding sites for soybean agglutinin lectin masked by sialylation are closely associated w
Masafumi, Abe:“对人伯基特淋巴瘤细胞系的凝集素结合特性进行分析,这些细胞系在 SCID 小鼠中表现出高自发性远处器官转移:被唾液酸化掩盖的大豆凝集素凝集素的结合位点与
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Masafumi, Abe: "Establishment and characterization of new human Burkitt's lymphoma cell lines (HBL-7 and HBL-8) that are highly metastatic in SCID mice : A metastatic SCID mouse model of human lymphoma lines" Pathology International. 46. 630-638 (1996)
Masafumi, Abe:“在 SCID 小鼠中高度转移的新型人类伯基特淋巴瘤细胞系(HBL-7 和 HBL-8)的建立和表征:人类淋巴瘤系的转移性 SCID 小鼠模型”病理学国际。
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Masafumi, Abe: "Analysis of lectin binding properties on human Burkitt's lymphoma cell lines that show high spontaneous metastasis to distant organs in SCID mice : The binding sites for soybean agglutinin lectin masked by sialylation are closely associate
Masafumi, Abe:“对 SCID 小鼠中表现出高自发性远处器官转移的人伯基特淋巴瘤细胞系的凝集素结合特性进行分析:被唾液酸化掩盖的大豆凝集素凝集素的结合位点密切相关
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ABE Masafumi其他文献

ABE Masafumi的其他文献

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{{ truncateString('ABE Masafumi', 18)}}的其他基金

Studvofbioloeical function of CD10/NEP24.11 protein on the B-cells
CD10/NEP24.11 蛋白对 B 细胞的生物学功能研究
  • 批准号:
    17590310
  • 财政年份:
    2005
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Molecular mechanism of the signaling pathway for execution of spontaneous apoptosis of human B-cell lymphoma
人B细胞淋巴瘤自发凋亡执行信号通路的分子机制
  • 批准号:
    12670168
  • 财政年份:
    2000
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Elucidation of apoptotic pathway of human B-cell lymphoma and its therapeutic application
人B细胞淋巴瘤凋亡途径的阐明及其治疗应用
  • 批准号:
    09670196
  • 财政年份:
    1997
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)

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使用人源化 SCID 小鼠分析泌尿系统癌症中的跨膜蛋白活性
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  • 批准号:
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Core B - SCID Mouse : Human Xenograft Core (Jordan Pober, MD/PhDP.I.)
核心 B - SCID 小鼠:人类异种移植核心(Jordan Pober,医学博士/博士)
  • 批准号:
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  • 财政年份:
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EXPERIMENTAL ANALYSIS OF VASCULER CHANGES IN CHRONIC ALLOGRAFT REJECTION USING HUMANIZED SCID MOUSE MODEL.
使用人源化 SCID 小鼠模型对慢性同种异体移植排斥中的血管变化进行实验分析。
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The heat shock protein(HSP) was investigated as the pathogenesis of focal infection with tonsil by the SCID mouse model
通过SCID小鼠模型研究热休克蛋白(HSP)作为扁桃体局灶性感染的发病机制
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Establishment of patient-like SCID mouse model by orthotopically implanting primary cultured cells from surgically-resected lung cancer tissues.
通过原位植入手术切除的肺癌组织的原代培养细胞建立类患者 SCID 小鼠模型。
  • 批准号:
    14571269
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