MOLECULAR PROBES FOR BURKITT'S AND MANTLE CELL LYMPHOMA
MOLECULAR PROBES FOR BURKITT'S AND MANTLE CELL LYMPHOMA
批准号:
6294221
负责人:
Nallasivam Palanisamy
金额:
$15.84万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-01-24 至 2001-08-31
中文摘要
申请人?本研究的目的是开发两种
荧光原位杂交(FISH)检测
t(11;14)(q13;q32)和t(8;14)(q24;q32)染色体易位
在曼特尔和伯基特街相遇s B细胞淋巴瘤。这些肿瘤
传统上通过放射和化学疗法治疗;然而,
复发并变得难以治疗。诊断和治疗后
通过流式细胞术、核型分析、Southern印迹或
PCR,其中每一种都具有特异性和/或灵敏度的限制。
因此,另一种精确、可靠、简便的检测肿瘤细胞的方法
特别是在标本的后处理中是必不可少的。这种方法就是FISH。
不幸的是,没有临床测试的探针可用于检测
不是曼托就是伯基特s淋巴瘤。在第一阶段的申请中,我们建议
开发基于BAC的探针以检测诊断中的易位携带核
并追踪病人样本每个染色体的探针将被标记
用不同的颜色,并将明确识别两个正常和
每个细胞核中有两条重排的染色体,从而提供了高特异性
和敏感性。
拟定商业应用:
拟议的研究将提供FISH检测,以检测t(11;14)(q13;q32)和
t(8;14)(q24;q32)染色体易位在套细胞淋巴瘤和
伯基特淋巴瘤,分别用于癌症细胞遗传学参考实验室。
英文摘要
APPLICANT?S DESCRIPTION: The goal of this research is to develop two
fluorescence in situ hybridization (FISH) assays for the detection of the
t(11;14)(q13;q32) and the t(8;14)(q24;q32) chromosomal translocations
encountered in Mantle and Burkitt?s B-cell Lymphoma respectively. These tumors
are traditionally treated by radiation and chemotherapy; however many patients
relapse and become refractory to treatment. Diagnosis and post-treatment
follow-up are performed by flow cytometry, karyotype, Southern Blotting, or
PCR, each of which has limitations of specificity and/or sensitivity.
Therefore, another precise, reliable, and easy method to detect tumor cells
especially in the post-treatment specimens is essential. Such a method is FISH.
Unfortunately, no clinically tested probes are available for the detection of
either Mantle or Burkitt?s Lymphoma. In this Phase I application, we propose to
develop BAC-based probes to detect translocation carrying nuclei in diagnostic
and follow up patient samples. The probes for each chromosome will be labeled
with a different color and will unambiguously identify the two normal and the
two rearranged chromosomes in each nucleus, thereby providing high specificity
and sensitivity.
PROPOSED COMMERCIAL APPLICATION:
The proposed research will provide FISH assays to detect the t(11;14)(q13;q32) and
t(8;14)(q24;q32) chromosomal translocations encountered in Mantle Cell Lymphoma and
Burkitt's Lymphoma, respectively, for use in cancer cytogenetic reference laboratories.
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