• 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

人类疾病的动物模型。携带并表达活化细胞癌基因的转基因小鼠中自发肿瘤的病理学和分子生物学。

Animal models of human disease. Pathology and molecular biology of spontaneous neoplasms occurring in transgenic mice carrying and expressing activated cellular oncogenes.

作者信息

Pattengale P K, Stewart T A, Leder A, Sinn E, Muller W, Tepler I, Schmidt E, Leder P

机构信息

Department of Pathology, Childrens Hospital, Los Angeles, CA 90027.

出版信息

Am J Pathol. 1989 Jul;135(1):39-61.

PMID:2672826
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1880223/
Abstract

This present review focuses on spontaneous neoplasms occurring in transgenic mice carrying and expressing activated cellular oncogenes. The historical development of transgenic mice as in vivo disease models is briefly traced, followed by a brief description of the actual technology in such systems. Additional emphasis is placed on the concept of targeting activated cellular oncogenes to specific tissues in transgenic mice. Cumulative experience with activated (Vmyc, ras, and neu (erb-B2] oncogenes in transgenic mice is considered in detail, with particular attention paid to the observed pathology, as well as to the kinetics of disease occurrence. It is concluded that transgenic mice offer the interested investigator(s) an excellent prospective, in vivo model of oncogenesis.

摘要

本综述聚焦于携带并表达活化细胞癌基因的转基因小鼠中发生的自发性肿瘤。简要追溯了转基因小鼠作为体内疾病模型的历史发展,随后简要描述了此类系统中的实际技术。还特别强调了将活化细胞癌基因靶向转基因小鼠特定组织的概念。详细讨论了转基因小鼠中活化(Vmyc、ras和neu(erb-B2))癌基因的累积经验,尤其关注观察到的病理学以及疾病发生的动力学。得出的结论是,转基因小鼠为感兴趣的研究者提供了一个出色的肿瘤发生体内前瞻性模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/7e6711c20a75/amjpathol00115-0060-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/c0b4e5c9b400/amjpathol00115-0052-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/62816244027b/amjpathol00115-0059-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/0ebf693ff207/amjpathol00115-0055-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/3819ae67ed84/amjpathol00115-0054-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/9a815606b7bd/amjpathol00115-0046-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/d27f04e829d6/amjpathol00115-0048-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/cefe31be1ec1/amjpathol00115-0049-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/2c4a7f56b44a/amjpathol00115-0050-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/2dbd27204000/amjpathol00115-0058-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/7e6711c20a75/amjpathol00115-0060-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/c0b4e5c9b400/amjpathol00115-0052-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/62816244027b/amjpathol00115-0059-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/0ebf693ff207/amjpathol00115-0055-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/3819ae67ed84/amjpathol00115-0054-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/9a815606b7bd/amjpathol00115-0046-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/d27f04e829d6/amjpathol00115-0048-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/cefe31be1ec1/amjpathol00115-0049-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/2c4a7f56b44a/amjpathol00115-0050-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/2dbd27204000/amjpathol00115-0058-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/1880223/7e6711c20a75/amjpathol00115-0060-a.jpg

相似文献

1
Animal models of human disease. Pathology and molecular biology of spontaneous neoplasms occurring in transgenic mice carrying and expressing activated cellular oncogenes.人类疾病的动物模型。携带并表达活化细胞癌基因的转基因小鼠中自发肿瘤的病理学和分子生物学。
Am J Pathol. 1989 Jul;135(1):39-61.
2
Transgenic models of human cancer.人类癌症的转基因模型。
Princess Takamatsu Symp. 1991;22:259-74.
3
[Spatio-temporal control of oncogenesis].[肿瘤发生的时空控制]
Pathol Biol (Paris). 1998 Feb;46(2):120-1.
4
Oncogene-induced liver neoplasia in transgenic mice.
Oncogene. 1989 Jun;4(6):715-24.
5
[Oncogenesis in transgenic mice].[转基因小鼠中的肿瘤发生]
Tsitologiia. 1994;36(2):131-47.
6
Activation of protooncogenes in spontaneously occurring non-liver tumors from C57BL/6 x C3H F1 mice.C57BL/6×C3H F1小鼠自发产生的非肝脏肿瘤中原癌基因的激活。
Cancer Res. 1991 Feb 15;51(4):1148-53.
7
[The role of proto-oncogenes in fundamental manifestations of life].
Eksp Onkol. 1990;12(6):14-26.
8
Embryonal tumors from transgenic mouse zygotes carrying human activated c-Ha-ras genes.携带人类活化型c-Ha-ras基因的转基因小鼠受精卵来源的胚胎性肿瘤
Mol Biol Med. 1989 Dec;6(6):567-72.
9
Regulatory imbalances in cell proliferation and cell death during oncogenesis in transgenic mice.转基因小鼠肿瘤发生过程中细胞增殖与细胞死亡的调控失衡。
Semin Cancer Biol. 1994 Feb;5(1):13-20.
10
Targeting oncogenes.靶向癌基因。
J Clin Invest. 2004 Nov;114(10):1362. doi: 10.1172/JCI23689.

引用本文的文献

1
Breast cancer animal models and applications.乳腺癌动物模型及应用。
Zool Res. 2020 Sep 18;41(5):477-494. doi: 10.24272/j.issn.2095-8137.2020.095.
2
Genetically Engineered Mouse Models for Liver Cancer.用于肝癌研究的基因工程小鼠模型。
Cancers (Basel). 2019 Dec 19;12(1):14. doi: 10.3390/cancers12010014.
3
Acidic Chitinase-Chitin Complex Is Dissociated in a Competitive Manner by Acetic Acid: Purification of Natural Enzyme for Supplementation Purposes.酸性几丁质酶-几丁质复合物在醋酸的竞争作用下解离:天然酶的补充纯化。

本文引用的文献

1
Nuclear transplantation in Mus musculus: developmental potential of nuclei from preimplantation embryos.小家鼠的核移植:植入前胚胎细胞核的发育潜能
Cell. 1981 Jan;23(1):9-18. doi: 10.1016/0092-8674(81)90265-8.
2
Transforming genes of carcinomas and neuroblastomas introduced into mouse fibroblasts.将癌和神经母细胞瘤的转化基因导入小鼠成纤维细胞。
Nature. 1981 Mar 19;290(5803):261-4. doi: 10.1038/290261a0.
3
Dramatic growth of mice that develop from eggs microinjected with metallothionein-growth hormone fusion genes.由显微注射金属硫蛋白-生长激素融合基因的卵发育而成的小鼠显著生长。
Int J Mol Sci. 2018 Jan 25;19(2):362. doi: 10.3390/ijms19020362.
4
Protease resistance of porcine acidic mammalian chitinase under gastrointestinal conditions implies that chitin-containing organisms can be sustainable dietary resources.在胃肠道条件下,猪酸性哺乳动物几丁质酶的抗蛋白酶性意味着含有几丁质的生物可以成为可持续的膳食资源。
Sci Rep. 2017 Oct 11;7(1):12963. doi: 10.1038/s41598-017-13526-6.
5
The transgenic cloned pig population with integrated and controllable GH expression that has higher feed efficiency and meat production.具有整合且可控生长激素(GH)表达、饲料效率更高且产肉量更高的转基因克隆猪群体。
Sci Rep. 2015 May 11;5:10152. doi: 10.1038/srep10152.
6
Activation of Akt1 accelerates carcinogen-induced tumorigenesis in mammary gland of virgin and post-lactating transgenic mice.Akt1的激活加速了处女和哺乳期后转基因小鼠乳腺中致癌物诱导的肿瘤发生。
BMC Cancer. 2014 Apr 17;14:266. doi: 10.1186/1471-2407-14-266.
7
14-3-3ζ orchestrates mammary tumor onset and progression via miR-221-mediated cell proliferation.14-3-3ζ 通过 miR-221 介导的细胞增殖来调控乳腺肿瘤的发生和发展。
Cancer Res. 2014 Jan 1;74(1):363-373. doi: 10.1158/0008-5472.CAN-13-2016. Epub 2013 Nov 6.
8
Mouse mammary gland is refractory to the effects of ethanol after natural lactation.自然泌乳后的小鼠乳腺对乙醇的作用具有抗性。
Comp Med. 2013 Feb;63(1):38-47.
9
In vivo imaging of lymph node migration of MNP- and (111)In-labeled dendritic cells in a transgenic mouse model of breast cancer (MMTV-Ras).在乳腺癌(MMTV-Ras)转基因小鼠模型中,MNP 和 (111)In 标记的树突状细胞的淋巴结迁移的体内成像。
Mol Imaging Biol. 2012 Apr;14(2):183-96. doi: 10.1007/s11307-011-0496-0.
10
Experimental models of hepatocellular carcinoma: developments and evolution.肝细胞癌实验模型:进展与演变
J Cancer Res Clin Oncol. 2009 Aug;135(8):969-81. doi: 10.1007/s00432-009-0591-7. Epub 2009 Apr 28.
Nature. 1982 Dec 16;300(5893):611-5. doi: 10.1038/300611a0.
4
Nuclear transplantation in the mouse embryo by microsurgery and cell fusion.通过显微手术和细胞融合对小鼠胚胎进行核移植。
Science. 1983 Jun 17;220(4603):1300-2. doi: 10.1126/science.6857250.
5
Translocation of the c-myc gene into the immunoglobulin heavy chain locus in human Burkitt lymphoma and murine plasmacytoma cells.在人类伯基特淋巴瘤和鼠浆细胞瘤细胞中,c-myc基因易位至免疫球蛋白重链基因座。
Proc Natl Acad Sci U S A. 1982 Dec;79(24):7837-41. doi: 10.1073/pnas.79.24.7837.
6
Experimental models of lymphoproliferative disease. The mouse as a model for human non-Hodgkin's lymphomas and related leukemias.淋巴增生性疾病的实验模型。小鼠作为人类非霍奇金淋巴瘤及相关白血病的模型。
Am J Pathol. 1983 Nov;113(2):237-65.
7
Gene transfer into mouse embryos: production of transgenic mice by pronuclear injection.基因导入小鼠胚胎:通过原核注射产生转基因小鼠。
Methods Enzymol. 1983;101:411-33. doi: 10.1016/0076-6879(83)01031-9.
8
Tissue-specific expression of the rat pancreatic elastase I gene in transgenic mice.大鼠胰腺弹性蛋白酶I基因在转基因小鼠中的组织特异性表达。
Cell. 1984 Oct;38(3):639-46. doi: 10.1016/0092-8674(84)90258-7.
9
Spontaneous mammary adenocarcinomas in transgenic mice that carry and express MTV/myc fusion genes.携带并表达MTV/ myc融合基因的转基因小鼠中的自发性乳腺腺癌。
Cell. 1984 Oct;38(3):627-37. doi: 10.1016/0092-8674(84)90257-5.
10
Partial correction of murine hereditary growth disorder by germ-line incorporation of a new gene.通过种系整合新基因对小鼠遗传性生长障碍进行部分校正。
Nature. 1984;311(5981):65-7. doi: 10.1038/311065a0.