• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Possible retroviral etiology of human breast cancer.

作者信息

Labat M L

出版信息

Biomed Pharmacother. 1998;52(1):6-12. doi: 10.1016/s0753-3322(97)86236-1.

DOI:10.1016/s0753-3322(97)86236-1
PMID:9755790
Abstract

Since the discovery in the early 1980s that retroviruses are pathogenic to man, the mouse mammary tumor viruses (MMTVs) received great attention. Studies of MMTVs allowed considerable insights into the mechanisms at work in breast tumorigenesis. MMTVs are essentially insertional mutagenes. Numerous oncogenes have been found altered by MMTVs, either specific for MMTVs or not. However, despite considerable attempts, the involvement of MMTVs in human breast cancer remains questionable. Yet a retroviral etiology of human breast cancer cannot be discarded since retroviruses are good candidates to play a role in diseases which, like human breast cancer, appear either as sporadic or inherited. Due to their replication cycle, retroviruses can be propagated not only as infectious agents able to freely infect host cells, but also as cellular genes which can be passed on to progeny. It is suggested here to search for a new human retrovirus in sporadic breast cancer, using the techniques which led to the isolation of human T-cell leukemia virus-1 (HTLV-1). Indeed, finding an infectious retrovirus in sporadic cases could lead, via the c-DNA probes derived from it, to testing the hypothesis that the inherited form of human breast cancer may result from the action of retroviral genes integrated in the germ line.

摘要

相似文献

1
Possible retroviral etiology of human breast cancer.
Biomed Pharmacother. 1998;52(1):6-12. doi: 10.1016/s0753-3322(97)86236-1.
2
A human murine mammary tumour virus-like agent is an unconvincing aetiological agent for human breast cancer.一种人类鼠类乳腺肿瘤病毒样因子作为人类乳腺癌的病因学因子并不令人信服。
Rev Med Virol. 2004 May-Jun;14(3):169-77. doi: 10.1002/rmv.427.
3
[The possibility of the retroviruses participation in human breast neoplasm induction].[逆转录病毒参与人类乳腺肿瘤诱发的可能性]
Vopr Virusol. 2002 Jul-Aug;47(4):4-9.
4
Revisiting a role for a mammary tumor retrovirus in human breast cancer.重新审视乳腺肿瘤逆转录病毒在人类乳腺癌中的作用。
Int J Cancer. 2013 Oct 1;133(7):1530-5. doi: 10.1002/ijc.28210. Epub 2013 May 15.
5
Human murine mammary tumour virus-like agents are genetically distinct from endogenous retroviruses and are not detectable in breast cancer cell lines or biopsies.人类鼠类乳腺肿瘤病毒样因子在基因上与内源性逆转录病毒不同,在乳腺癌细胞系或活检样本中无法检测到。
Virology. 2004 Jan 5;318(1):393-404. doi: 10.1016/j.virol.2003.09.027.
6
Mouse mammary tumor viruses expressed by RIII/Sa mice with a high incidence of mammary tumors interact with the V beta-2- and V beta-8-specific T cells during viral infection.具有高乳腺肿瘤发病率的RIII/Sa小鼠所表达的小鼠乳腺肿瘤病毒在病毒感染期间与Vβ-2和Vβ-8特异性T细胞相互作用。
Virology. 2003 Sep 15;314(1):294-304. doi: 10.1016/s0042-6822(03)00429-x.
7
Retroviruses and bone diseases.逆转录病毒与骨疾病
Clin Orthop Relat Res. 1996 May(326):287-309. doi: 10.1097/00003086-199605000-00036.
8
[The human mammary tumor virus (HMTV) in 2014].[2014年的人类乳腺肿瘤病毒(HMTV)]
Medicina (B Aires). 2014;74(5):415-7.
9
MMTV-induced mutations in mouse mammary tumors: their potential relevance to human breast cancer.MMTV诱导的小鼠乳腺肿瘤中的突变:它们与人类乳腺癌的潜在相关性。
Breast Cancer Res Treat. 1996;39(1):33-44. doi: 10.1007/BF01806076.
10
[Searching for retroviral sequences related to human breast cancer].[寻找与人类乳腺癌相关的逆转录病毒序列]
Medicina (B Aires). 1997;57 Suppl 2:75-80.

引用本文的文献

1
Two hypotheses of dense breasts and viral infection for explaining incidence of breast cancer by age group in Korean women.两种假说解释韩国女性乳腺癌发病率随年龄组变化的原因:致密乳房和病毒感染。
Epidemiol Health. 2014 Sep 26;36:e2014020. doi: 10.4178/epih/e2014020. eCollection 2014.