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[默克尔细胞多瘤病毒与默克尔细胞癌]

[Merkel cell polyomavirus and Merkel cell carcinoma].

作者信息

Nakamura Tomoyuki, Katano Harutaka

机构信息

Department of Pathology, National Institute of Infectious Diseases.

出版信息

Uirusu. 2009 Jun;59(1):37-42. doi: 10.2222/jsv.59.37.

Abstract

A new polyomavirus, Merkel cell polyomavirus, was identified from Merkel cell carcinoma, a rare skin cancer. Origin of Merkel cell carcinoma is Merkel cell, a neuroendocrine cell in the skin. Merkel cell carcinoma occurs in the skin of head and face of white elders. Like other polyomaviruses, a 5.4 kbp-virus genome encodes VP1, VP2, VP3, small T antigen, and large T (LT) antigen. MCV has been frequently detected in Merkel cell carcinoma in the world by PCR. It was demonstrated that MCV genome integrated into the host genome of Merkel cell carcinoma. LT plays an important role in replication of a circular MCV. However, mutations with stop codons were identified in the LT genes derived from Merkel cell carcinoma cases. Such mutations cause a truncation of the LT gene, resulting in defect of LTs helicase activity and in induction of Rb binding function in the LT. MCV is a new member of human oncovirus belonging to the human polyomavirus.

摘要

一种新的多瘤病毒,默克尔细胞多瘤病毒,是从默克尔细胞癌(一种罕见的皮肤癌)中鉴定出来的。默克尔细胞癌起源于默克尔细胞,一种皮肤中的神经内分泌细胞。默克尔细胞癌发生在白人老年人的头面部皮肤。与其他多瘤病毒一样,一个5.4千碱基对的病毒基因组编码VP1、VP2、VP3、小T抗原和大T(LT)抗原。通过聚合酶链反应(PCR)在全球范围内的默克尔细胞癌中经常检测到默克尔细胞多瘤病毒(MCV)。已证明MCV基因组整合到默克尔细胞癌的宿主基因组中。LT在环状MCV的复制中起重要作用。然而,在来自默克尔细胞癌病例的LT基因中鉴定出了带有终止密码子的突变。这种突变导致LT基因截短,从而导致LT解旋酶活性缺陷以及LT中Rb结合功能的诱导缺陷。MCV是属于人类多瘤病毒的人类肿瘤病毒的新成员。

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