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伴有间变性大细胞淋巴瘤激酶融合基因的炎性肌纤维母细胞瘤中无人类疱疹病毒8型和EB病毒。

Absence of human herpesvirus-8 and Epstein-Barr virus in inflammatory myofibroblastic tumor with anaplastic large cell lymphoma kinase fusion gene.

作者信息

Yamamoto Hidetaka, Kohashi Kenichi, Oda Yoshinao, Tamiya Sadafumi, Takahashi Yukiko, Kinoshita Yoshiaki, Ishizawa Shin, Kubota Masayuki, Tsuneyoshi Masazumi

机构信息

Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

Pathol Int. 2006 Oct;56(10):584-90. doi: 10.1111/j.1440-1827.2006.02012.x.

Abstract

Inflammatory myofibroblastic tumor (IMT) is clinically and histologically characterized by inflammation. Some populations of IMT have anaplastic large cell lymphoma kinase (ALK) gene rearrangements. Infection with Epstein-Barr virus (EBV) and human herpesvirus-8 (HHV-8) in tumor cells of IMT has been reported; these reports, however, have been limited to ALK-negative IMT. The purpose of the present paper was to evaluate 21 cases of IMT for the presence of EBV and HHV-8. Immunohistochemically, 15 cases were ALK positive and six were negative. Of eight cases analyzed using reverse transcription-polymerase chain reaction, tropomyosin 3 (TPM3)-ALK, TPM4-ALK and clathrin heavy chain-ALK fusion genes were detected in one, two and two cases, respectively. All 21 IMT, irrespective of ALK expression, were negative for EBV by in situ hybridization for EBV-encoded RNA and immunohistochemical stain for latent membrane antigen-1. HHV-8 was also negative in all IMT by PCR for HHV-8 DNA sequence (KS330/233) and immunohistochemical stain for latent nuclear antigen. These results suggest that IMT may be a heterogeneous group in terms of pathogenesis, and EBV and HHV-8 do not play a major role in the pathogenesis of ALK-positive tumor.

摘要

炎性肌纤维母细胞瘤(IMT)在临床和组织学上以炎症为特征。部分IMT人群存在间变性大细胞淋巴瘤激酶(ALK)基因重排。已有报道称IMT肿瘤细胞中存在爱泼斯坦-巴尔病毒(EBV)和人类疱疹病毒8型(HHV-8)感染;然而,这些报道仅限于ALK阴性的IMT。本文旨在评估21例IMT中EBV和HHV-8的存在情况。免疫组化结果显示,15例为ALK阳性,6例为阴性。在使用逆转录-聚合酶链反应分析的8例病例中,分别在1例、2例和2例中检测到原肌球蛋白3(TPM3)-ALK、TPM4-ALK和网格蛋白重链-ALK融合基因。通过针对EBV编码RNA的原位杂交和针对潜伏膜抗原-1的免疫组化染色,所有21例IMT,无论ALK表达情况如何,EBV均为阴性。通过针对HHV-8 DNA序列(KS330/233)的PCR和针对潜伏核抗原的免疫组化染色,所有IMT中的HHV-8也均为阴性。这些结果表明,IMT在发病机制方面可能是一个异质性群体,并且EBV和HHV-8在ALK阳性肿瘤的发病机制中不发挥主要作用。

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