• 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

在裸鼠体内生长的人肿瘤细胞系的转移行为。

Metastatic behavior of human tumor cell lines grown in the nude mouse.

作者信息

Kozlowski J M, Fidler I J, Campbell D, Xu Z L, Kaighn M E, Hart I R

出版信息

Cancer Res. 1984 Aug;44(8):3522-9.

PMID:6744277
Abstract

The metastatic behavior of seven human tumor cell lines grown in young (3- to 4-week-old) nude mice was studied. Two cell lines were derived from malignant melanomas, one from a colon carcinoma, two from prostate adenocarcinomas, and two from renal adenocarcinomas. Many of the cell lines produced metastases after i.v. injection (experimental metastasis) and after s.c. transplantation (spontaneous metastasis) into young nude mice. The incidence of metastasis seemed dependent primarily on the biological characteristics of the individual tumor cell line. However, the incidence of metastasis of some tumor cell lines could be increased by isolation and establishment of variant sublines from secondary tumor deposits, by prolonged systemic administration of 17 beta-estradiol to suppress natural killer cell activity, and/or by use of an advantageous site of tumor implantation. Intrasplenic injection of tumor cells allowed the most dramatic overall expression of metastatic capacity in these cell lines, resulting in frequent and large metastases to liver, lungs, and the mesenteric, omental, and mediastinal lymph nodes.

摘要

对在年轻(3至4周龄)裸鼠体内生长的七种人类肿瘤细胞系的转移行为进行了研究。其中两种细胞系源自恶性黑色素瘤,一种源自结肠癌,两种源自前列腺腺癌,还有两种源自肾腺癌。许多细胞系在静脉注射(实验性转移)以及皮下移植(自发性转移)到年轻裸鼠体内后都会产生转移。转移发生率似乎主要取决于各个肿瘤细胞系的生物学特性。然而,某些肿瘤细胞系的转移发生率可通过从继发性肿瘤沉积物中分离并建立变异亚系、长期全身性给予17β-雌二醇以抑制自然杀伤细胞活性和/或通过使用有利的肿瘤植入部位来提高。脾内注射肿瘤细胞能使这些细胞系的转移能力得到最显著的整体表现,导致频繁且大量地转移至肝脏、肺以及肠系膜、网膜和纵隔淋巴结。

相似文献

1
Metastatic behavior of human tumor cell lines grown in the nude mouse.在裸鼠体内生长的人肿瘤细胞系的转移行为。
Cancer Res. 1984 Aug;44(8):3522-9.
2
Metastatic behavior of tumor cells isolated from primary and metastatic human colorectal carcinomas implanted into different sites in nude mice.从原发性和转移性人类结直肠癌中分离出的肿瘤细胞植入裸鼠不同部位后的转移行为。
Cancer Res. 1986 Apr;46(4 Pt 2):1928-33.
3
Growth and metastasis of tumor cells isolated from a human renal cell carcinoma implanted into different organs of nude mice.从植入裸鼠不同器官的人肾细胞癌中分离出的肿瘤细胞的生长和转移。
Cancer Res. 1986 Aug;46(8):4109-15.
4
Expression of metastatic potential of allogenic and xenogeneic neoplasms in young nude mice.年轻裸鼠同种异体和异种肿瘤转移潜能的表达
Cancer Res. 1981 Feb;41(2):438-44.
5
Influence of organ environment on the growth, selection, and metastasis of human colon carcinoma cells in nude mice.器官环境对人结肠癌细胞在裸鼠体内生长、筛选及转移的影响。
Cancer Res. 1988 Dec 1;48(23):6863-71.
6
Malignant potential of cells isolated from lymph node or brain metastases of melanoma patients and implications for prognosis.从黑色素瘤患者的淋巴结或脑转移灶中分离出的细胞的恶性潜能及其对预后的影响。
Cancer Res. 1991 Apr 15;51(8):2029-35.
7
Enhanced experimental metastatic capacity of a human tumor line following treatment with 5-azacytidine.5-氮杂胞苷处理后人肿瘤细胞系实验性转移能力增强。
Cancer Res. 1986 Feb;46(2):884-90.
8
Establishment of a hepatocellular carcinoma cell line with unique metastatic characteristics through in vivo selection and screening for metastasis-related genes through cDNA microarray.通过体内筛选建立具有独特转移特性的肝癌细胞系,并通过cDNA微阵列筛选转移相关基因。
J Cancer Res Clin Oncol. 2003 Jan;129(1):43-51. doi: 10.1007/s00432-002-0396-4. Epub 2002 Dec 4.
9
A human melanoma line heterogeneous with respect to metastatic capacity in athymic nude mice.一种在无胸腺裸鼠中转移能力存在异质性的人黑色素瘤细胞系。
J Natl Cancer Inst. 1984 Apr;72(4):913-7.
10
Methods of immunosuppression for study of growth and lung colony formation by human tumor cells in mice.用于研究人肿瘤细胞在小鼠体内生长和肺集落形成的免疫抑制方法。
Cancer Res. 1986 Apr;46(4 Pt 1):1617-22.

引用本文的文献

1
Targeting TRPV6/CXCR4 complexes prevents castration-resistant prostate cancer metastasis to the bone.靶向TRPV6/CXCR4复合物可预防去势抵抗性前列腺癌向骨转移。
Signal Transduct Target Ther. 2025 Sep 5;10(1):287. doi: 10.1038/s41392-025-02376-8.
2
Cancer metastasis to the bone: Mechanisms and animal models (Review).癌症骨转移:机制与动物模型(综述)
Oncol Lett. 2025 Mar 6;29(5):221. doi: 10.3892/ol.2025.14967. eCollection 2025 May.
3
EphA2 regulates vascular permeability and prostate cancer metastasis via modulation of cell junction protein phosphorylation.
EphA2通过调节细胞连接蛋白磷酸化来调控血管通透性和前列腺癌转移。
Oncogene. 2025 Feb;44(4):208-227. doi: 10.1038/s41388-024-03206-x. Epub 2024 Nov 7.
4
Therapeutic Effects of Essential Oils and Their Bioactive Compounds on Prostate Cancer Treatment.精油及其生物活性化合物对前列腺癌治疗的疗效
Pharmaceutics. 2024 Apr 24;16(5):583. doi: 10.3390/pharmaceutics16050583.
5
FABP5 can substitute for androgen receptor in malignant progression of prostate cancer cells.FABP5 可在前列腺癌细胞的恶性进展中替代雄激素受体。
Int J Oncol. 2024 Feb;64(2). doi: 10.3892/ijo.2023.5606. Epub 2023 Dec 22.
6
Animal models of bone metastatic prostate cancer.骨转移前列腺癌动物模型。
Investig Clin Urol. 2023 May;64(3):219-228. doi: 10.4111/icu.20230026.
7
NALCN-mediated sodium influx confers metastatic prostate cancer cell invasiveness.NALCN 介导的钠离子内流赋予转移性前列腺癌细胞侵袭性。
EMBO J. 2023 Jul 3;42(13):e112198. doi: 10.15252/embj.2022112198. Epub 2023 Jun 6.
8
Regulating lactate-related immunometabolism and EMT reversal for colorectal cancer liver metastases using shikonin targeted delivery.利用紫草素靶向递送来调节乳酸相关的免疫代谢和 EMT 逆转治疗结直肠癌肝转移。
J Exp Clin Cancer Res. 2023 May 10;42(1):117. doi: 10.1186/s13046-023-02688-z.
9
Traject3d allows label-free identification of distinct co-occurring phenotypes within 3D culture by live imaging.Traject3d 通过实时成像实现了 3D 培养物中无标记的独特共现表型的鉴定。
Nat Commun. 2022 Sep 9;13(1):5317. doi: 10.1038/s41467-022-32958-x.
10
Compromised activity of natural killer cells in diffuse large b-cell lymphoma is related to lymphoma-induced modification of their surface receptor expression.弥漫性大 B 细胞淋巴瘤中自然杀伤细胞活性受损与淋巴瘤诱导的表面受体表达改变有关。
Cancer Immunol Immunother. 2023 Mar;72(3):707-718. doi: 10.1007/s00262-022-03284-4. Epub 2022 Sep 1.