期刊文献+

实时定量PCR检测Bcl-2/IgH融合基因在淋巴瘤中的应用

Application of Real-time Quantitative PCR Detecting Bcl-2/IgH Fusion Gene in Lymphoma
下载PDF
导出
摘要 Bcl-2/IgH融合基因是淋巴瘤的肿瘤特异性标志,见于85%~90%的滤泡性淋巴瘤及30%的弥漫性大B细胞淋巴瘤患者。大量研究表明,该融合基因与滤泡性淋巴瘤和弥漫性大B细胞淋巴瘤有很好的相关性,对Bcl-2/IgH的定量检测能反应淋巴瘤的临床进程。现就实时定量PCR技术对Bcl-2/IgH融合基因的检测在淋巴瘤的分期、疗效评价、预测复发和预后评估等方面的临床意义进行综述。 The Bcl-2/IgH fusion gene is the specific mark of malignant lymphoma.It was expressed in 85%~90% cases of follicular lymphoma(FL) and 30% diffuse large B-cell lymphoma(DLBCL).Studies showed that this fusion gene has good correlativity with follicular lymphoma and diffuse large B-cell lymphoma,and the quantitative detection of this fusion gene can reflect the clinical process of lymphoma.This article reviews clinical significance of Bcl-2/IgH fusion gene detection by RQ-PCR in the staging,evaluation of curative effect,prediction of recurrence,and prognostic evaluation.
作者 徐明 张学美
出处 《医学综述》 2008年第6期811-813,共3页 Medical Recapitulate
关键词 BCL-2/IGH 融合基因 淋巴瘤 实时定量聚合酶链反应 Bcl-2/IgH Fusion gene Lymphoma Real-Time Quantitative polymerase chain reaction
  • 相关文献

参考文献21

  • 1Gribben JG, Freedman AS, Woo SD, et al. All advanced stage NonHodgkin's lmphomas with a polymerase chain reaction amplifiable breakpoint of bcl-2 have residual ceils containing the bcl-2 rearrangment at evaluation and after treatment [ J ]. Blood, 1991,78 (12) :3275-3280.
  • 2Tsujimoto Y, Finger LR, Yunis J, et al. Cloning of the chromosome breakpoint of neoplastic B cell with the t( 14; 18) chromosome transloeation [ J ]. Science, 1984,226 ( 4678 ) : 1097 -1099.
  • 3朱宏丽,汪月增.t(14;18)易位的分子基础和致病机理[J].国外医学(输血及血液学分册),1996,19(2):72-74. 被引量:2
  • 4Akasaka T,Akasaka H,Yonetani N,et al. Refinement of the bcl-2/ immunoglobulin heavy chain fusion gene in t( 14 ; 18 ) ( q32 ; q21 ) by polymerase chain reaction amplification for long target [ J ]. Genes Chromosomes Cancer, 1998,21 ( 1 ) : 17-29.
  • 5Dolken G, Illerhaus G, Hirt C, et al. Bcl-2/JH rearrangements in circulating B ceils of healthy blood donors and patients with nonmalignant disease [ J ]. J Clin Oncol, 1996,14 (4) : 1333 -1334.
  • 6石岚,李惠民.实时定量PCR检测IgH重排在B淋巴细胞恶性肿瘤中的应用[J].白血病.淋巴瘤,2005,14(3):189-191. 被引量:2
  • 7Bothling SD, King TC, Wittwer CT, et al. Rapid simuhaneous amplification and detection of the MBR/JH chromosomal translocation by fluorescence melting curve analysis [ J ]. Am J Pathol, 1999,154 (2) :97-103.
  • 8Luthra R, McBride JA, CabaniBas F, et al. Novel 5' exonuclease- based real-time PCR assay for the detection of t( 14; 18) (q32; q21 ) in patients with follicular lymphoma[ J]. Am J Pathol,1998, 153(1) :63-68.
  • 9蒋一强,陈燕,李慧玉.非霍奇金淋巴瘤bcl-2/IgH基因重排及在微小残留病变检测中的应用[J].癌症,1999,18(4):400-403. 被引量:3
  • 10Yuan R, Dowling P, Zucca E, et al. Detection of bcl-2/JH rearrangement in follicular and diffuse lymphoma:concordant results of peripheral blood and bone marrow analysis at diagnosis [ J ]. Br J Cancer, 1993,67 (5) :922-925.

二级参考文献41

  • 1Shi S K,J Histochem Cytochem,1991年,39卷,741页
  • 2Shipp MA, Abeloff MD, Antman KH, et al. International consensus conference on high-dose therapy with hematopoietic stem cell transplantation in aggressive non-Hodgkin′s lymphomas: report of the jury. J Clin Oncol, 1999, 17:423-429.
  • 3Zwicky CS, Maddocks AB, Anderson N, et al. Eradication of polymerase chain reaction detectable immunoglobulin gene rearrangement in non-Hodgkin′s lymphoma is associated with decreased relapse after autologous bone marrow transplantation. Blood, 1996, 88:3314-3322.
  • 4Leonard B, Hetu F, Busque L, et al. Lymphoma cell burden in progenitor cell grafts measured by competitive polymerase chain reaction: less than one log difference between bone marrow and peripheral blood sources. Blood, 1998, 91:331-339.
  • 5Signoretto S, Murphy M, Cangi MG, et al. Detection of clonal T-cell receptor γ Gene rearramgements in paraffin-embeded tissue by polymerase chain reaction and nonradioactive single-strand conformational polymorphism analysis. Am J Pathol, 1999,154:62-76.
  • 6Baruchel A, Cayuela JM, MacIntyre E, et al. Assessment of clonal evolution at Ig/TCR loci in acute lymphoblastic leukaemia by single-strand conformation polymorphism studies and highly resolutive PCR derived methods:implication for a general strategy of minimal residual disease detection. Br J Haematol, 1995, 90:85-93.
  • 7Pappa VI, Wilkes S, Salam A, et al. Use of the polymerase chain reaction and direct sequencing analysis to detect cells with the t(14;18) in autologous bone marrow from patients with follicular lymphoma before and after in vitro treatment. Bone Marrow Transplant, 1998, 22:553-558.
  • 8Jacquy C, Lambert F, Soree A, et al. Peripheral blood stem cell contamination in mantle cell non-Hodgkin lymphoma: the case for purging? Bone Marrow Transplant, 1999, 23:681-686.
  • 9Kanteti R, Miller K, McCann JC, et al. Randomized trial of peripheral blood progenitor cell vs bone marrow as hematopoietic support for high-dose chemotherapy in patients with non-Hodgkin′s lymphoma and Hodgkin′s disease: a clinical and molecular analysis. Bone Marrow Transplant, 1999, 24:473-481.
  • 10Blystad AK, Kvalheim G, Torlakovic E, et al. High-dose therapy supported with immunomagnetic purged autologous bone marrow in high-grade B cell non-Hodgkin′s lymphoma. Bone Marrow Transplant, 1999, 24:865-872.

共引文献25

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部