[Correlation between C-MYC protein expression and genetic abnormalities in diffuse large B-cell lymphoma]

Zhonghua Bing Li Xue Za Zhi. 2018 Mar 8;47(3):172-175. doi: 10.3760/cma.j.issn.0529-5807.2018.03.005.
[Article in Chinese]

Abstract

Objective: To study the correlation between expression of oncogene C-MYC protein and gene abnormality in diffuse large B-cell lymphoma (DLBCL). Methods: The expression of C-MYC protein and gene abnormality were detected by immunohistochemistry and fluorescence in situ hybridization (FISH), respectively, in 42 cases of paraffin-embedded DLBCL. All cases were collected at Department of Pathology, Weifang People's Hospital during January 2015 to October 2016. Results: The positive rate of C-MYC protein expression was 47.6% (20/42) and the rate of abnormal C-MYC gene by FISH was 26.2%(11/42), including translocation (23.8%, 10/42) and gene amplification (2.4%, 1/42). There was a close relationship between the protein expression and gene translocation (χ(2)=11.813; P=0.001) and gene translocation occurred primarily in GCB (χ(2)=4.029; P=0.045). Conclusion: The high expression (≥40%) of C-MYC protein is associated with its gene translocation, suggesting that C-MYC protein detection can be used as a surrogate marker for C-MYC gene translocation in DLBCL.

目的:探讨弥漫性大B细胞淋巴瘤(DLBCL)中癌基因C-MYC蛋白表达及与基因异常的相关性。 方法:回顾性收集山东省潍坊市人民医院病理科2015年1月至2016年10月首次诊断为DLBCL的石蜡包埋组织标本42例,采用免疫组织化学和荧光原位杂交(FISH)技术检测全部研究对象组织标本中C-MYC蛋白表达与基因异常的情况,观察两者之间的相关性。 结果: C-MYC蛋白表达阳性率为47.6%(20/42);C-MYC基因异常检出率为26.2%(11/42),其中基因易位检出率23.8%(10/42);基因扩增2.4%(1/42);C-MYC蛋白表达阳性与C-MYC基因易位有相关性(χ(2)=11.813;P=0.001);C-MYC基因易位主要见于生发中心B细胞型(χ(2)=4.029;P=0.045)。 结论: C-MYC蛋白表达阳性(≥40%)与C-MYC基因易位有相关性。在DLBCL中,C-MYC蛋白高表达提示可能存在C-MYC基因易位。.

Keywords: Gene amplification; Lymphoma, large B-cell, diffuse; Proto-oncogene proteins c-myc.

MeSH terms

  • Gene Amplification
  • Genes, myc*
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization, Fluorescence
  • Lymphoma, Large B-Cell, Diffuse / genetics*
  • Lymphoma, Large B-Cell, Diffuse / metabolism*
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins c-myc / metabolism*
  • Translocation, Genetic

Substances

  • MAS1 protein, human
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins c-myc