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Loss of heterozygosity on chromosome 22 in sporadic schwannoma and its relation to the proliferation of tumor cells

BIAN Liu-guan SUN Qing-fang Tirakotai Wuttipong ZHAO Wei-guo SHEN Jian-kang LUO Qi-zhong Bertalanffy Helmut

中华医学杂志(英文版)2005,Vol.118Issue(18):1517-1524,8.
中华医学杂志(英文版)2005,Vol.118Issue(18):1517-1524,8.

Loss of heterozygosity on chromosome 22 in sporadic schwannoma and its relation to the proliferation of tumor cells

Loss of heterozygosity on chromosome 22 in sporadic schwannoma and its relation to the proliferation of tumor cells

BIAN Liu-guan 1SUN Qing-fang 2Tirakotai Wuttipong 1ZHAO Wei-guo 2SHEN Jian-kang 1LUO Qi-zhong 1Bertalanffy Helmut3

作者信息

  • 1. Department of Neurosurgery, Ruijin Hospital, Shanghai Second Medical University, Shanghai 200025, China
  • 2. Department of Neurosurgery, Philipps University, Marburg 35033, Germany
  • 3. Department of Neurosurgery, Renji Hospital, Shanghai Second Medical University, Shanghai 200025, China
  • 折叠

摘要

Abstract

Background Schwannoma is the tumor arising mainly from the cranial and spinal nerves. Bilateral vestibular schwannoma is the hallmark of neurofibromatosis type 2 (NF2). The NF2 gene has been cloned with comprehensive analysis of its mutations in schwannoma. However, most studies focused on vestibular schwannoma. There are differences in proliferation of tumor cell and ultrastructure between vestibular and spinal schwannomas. It is unknown whether genetic alterations in vestibular schwannoma are different from those in non-vestibular schwannoma. We analyzed the loss of heterozygosity (LOH) on chromosome 22 in patients with sporadic schwannoma including vestibular and spinal schwannomas and correlated this genetic alteration with tumor proliferation. Methods In 54 unrelated patients without clinical NF1 or NF2, 36 patients had sporadic vestibular schwannoma, and 18 dorsal spinal root schwannoma. Four highly polymorphic linkage to NF2 gene microsatellite DNA markers (D22S264, D22S268, D22S280, CRYB2) were used to analyze LOH. The proliferative index was evaluated by Ki-67 and proliferative cell nuclear antigen (PCNA) immunostaining. Student's t test was used to analyze the difference of the proliferative index between schwannoma with LOH and that without LOH. The difference of the frequency of LOH in vestibular and spinal schwannomas was investigated by the chi-square test. Results Twenty-three schwannomas (42.6%, 23/54) showed allele loss. The frequency of LOH in vestibular schwannoma was significantly higher than that in spinal schwannoma (χ2=5.14, P<0.05). The proliferative index of schwannoma with LOH was significantly higher than that without LOH (tki-67=2.97, P=0.0045; tPCNA=2.93, P=0.0051). Conclusions LOH on chromosome 22 is a frequent event in the tumorigenesis of sporadic schwannoma. And, there is a correlation between LOH on chromosome 22 and proliferative activity in schwannoma. The frequency of LOH in vestibular schwannoma is significantly different from that in spinal schwannoma.

关键词

schwannomas/loss of heterozygosity/chromosome 22

Key words

schwannomas/loss of heterozygosity/chromosome 22

分类

医药卫生

引用本文复制引用

BIAN Liu-guan,SUN Qing-fang,Tirakotai Wuttipong,ZHAO Wei-guo,SHEN Jian-kang,LUO Qi-zhong,Bertalanffy Helmut..Loss of heterozygosity on chromosome 22 in sporadic schwannoma and its relation to the proliferation of tumor cells[J].中华医学杂志(英文版),2005,118(18):1517-1524,8.

基金项目

This study was supported by a grant from the Natural Science Foundation of Shanghai (No. 03ER140009) and a grant from the Phosphorus Plan of Shanghai Municipal Commission of Science and Technology (04qmh144). (No. 03ER140009)

中华医学杂志(英文版)

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