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1
Altered expression of epidermal growth factor receptor gene in a classical multidrug-resistant variant of a human cancer cell line, KB.人癌细胞系KB的经典多药耐药变体中表皮生长因子受体基因的表达改变。
Jpn J Cancer Res. 1989 Apr;80(4):373-9. doi: 10.1111/j.1349-7006.1989.tb02322.x.
2
Isolation of human KB cell lines resistant to epidermal growth factor-Pseudomonas exotoxin conjugates.对表皮生长因子-铜绿假单胞菌外毒素偶联物具有抗性的人KB细胞系的分离
Cancer Res. 1987 Jun 1;47(11):2961-6.
3
Genetic characterization of human KB cell lines resistant to epidermal growth factor: Pseudomonas exotoxin conjugates.
J Cell Physiol. 1988 Jun;135(3):527-32. doi: 10.1002/jcp.1041350323.
4
Mutant KB cells with decreased EGF receptor expression: biochemical characterization.表皮生长因子受体表达降低的突变型KB细胞:生化特性
J Cell Physiol. 1987 Oct;133(1):127-34. doi: 10.1002/jcp.1041330116.
5
Epidermal growth factor receptor is increased in multidrug-resistant Chinese hamster and mouse tumor cells.表皮生长因子受体在多药耐药的中国仓鼠和小鼠肿瘤细胞中增加。
Proc Natl Acad Sci U S A. 1986 Aug;83(15):5521-5. doi: 10.1073/pnas.83.15.5521.
6
Epidermal growth factor receptor-dependent cytotoxicity for human squamous carcinoma cell lines of a conjugate composed of human EGF and RNase 1.人表皮生长因子(EGF)与核糖核酸酶1(RNase 1)缀合物对人鳞状癌细胞系的表皮生长因子受体依赖性细胞毒性
Life Sci. 1996;58(21):1901-8. doi: 10.1016/0024-3205(96)00174-9.
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Altered epidermal growth factor (EGF)-stimulated protein kinase activity in variant A431 cells with altered growth responses to EGF.在对表皮生长因子(EGF)生长反应改变的A431变异细胞中,EGF刺激的蛋白激酶活性发生改变。
Proc Natl Acad Sci U S A. 1982 Apr;79(8):2574-8. doi: 10.1073/pnas.79.8.2574.
8
Two independent mechanisms for escaping epidermal growth factor-mediated growth inhibition in epidermal growth factor receptor-hyperproducing human tumor cells.在表皮生长因子受体高表达的人类肿瘤细胞中,存在两种独立的机制来逃避表皮生长因子介导的生长抑制。
J Cell Biol. 1988 Aug;107(2):791-9. doi: 10.1083/jcb.107.2.791.
9
Altered degradation of epidermal growth factor in a diphtheria toxin-resistant clone of KB cells.KB细胞的白喉毒素抗性克隆中表皮生长因子降解的改变。
J Cell Physiol. 1985 Aug;124(2):322-30. doi: 10.1002/jcp.1041240223.
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Reduced endocytosis and altered lysosome function in cisplatin-resistant cell lines.顺铂耐药细胞系中内吞作用减弱及溶酶体功能改变。
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本文引用的文献

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Genetics of cell surface receptors for bioactive polypeptides: binding of epidermal growth factor is associated with the presence of human chromosome 7 in human-mouse cell hybrids.生物活性多肽细胞表面受体的遗传学:表皮生长因子的结合与人鼠细胞杂种中人7号染色体的存在相关。
Proc Natl Acad Sci U S A. 1980 Jun;77(6):3600-4. doi: 10.1073/pnas.77.6.3600.
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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.一种将DNA限制性内切酶片段放射性标记至高比活度的技术。
Anal Biochem. 1983 Jul 1;132(1):6-13. doi: 10.1016/0003-2697(83)90418-9.
3
Cell surface P-glycoprotein associated with multidrug resistance in mammalian cell lines.与哺乳动物细胞系中的多药耐药性相关的细胞表面P-糖蛋白。
Science. 1983 Sep 23;221(4617):1285-8. doi: 10.1126/science.6137059.
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DNA-mediated transfer of multiple drug resistance and plasma membrane glycoprotein expression.DNA介导的多重耐药性转移与质膜糖蛋白表达
Mol Cell Biol. 1982 Aug;2(8):881-9. doi: 10.1128/mcb.2.8.881-889.1982.
5
Monoclonal antibodies to glycoproteins of Vinca alkaloid-resistant human leukemic cells.针对长春花生物碱抗性人白血病细胞糖蛋白的单克隆抗体。
Cancer Res. 1985 Jul;45(7):3220-4.
6
Multiply drug-resistant human KB carcinoma cells have decreased amounts of a 75-kDa and a 72-kDa glycoprotein.多重耐药的人KB癌细胞中的一种75千道尔顿和一种72千道尔顿糖蛋白的含量减少。
Proc Natl Acad Sci U S A. 1985 Apr;82(8):2330-3. doi: 10.1073/pnas.82.8.2330.
7
Isolation and genetic characterization of human KB cell lines resistant to multiple drugs.对多种药物耐药的人KB细胞系的分离与遗传特征分析
Somat Cell Mol Genet. 1985 Mar;11(2):117-26. doi: 10.1007/BF01534700.
8
Mammalian multidrug resistance gene: complete cDNA sequence indicates strong homology to bacterial transport proteins.哺乳动物多药耐药基因:完整的cDNA序列表明其与细菌转运蛋白具有高度同源性。
Cell. 1986 Nov 7;47(3):371-80. doi: 10.1016/0092-8674(86)90594-5.
9
Multiple drug-resistant human KB carcinoma cells independently selected for high-level resistance to colchicine, adriamycin, or vinblastine show changes in expression of specific proteins.对秋水仙碱、阿霉素或长春花碱具有高水平抗性的多重耐药性人KB癌细胞系,经独立筛选后,其特定蛋白质的表达会发生变化。
J Biol Chem. 1986 Jun 15;261(17):7762-70.
10
Cytogenetic alterations associated with the acquisition of doxorubicin resistance: possible significance of chromosome 7 alterations.与阿霉素耐药性获得相关的细胞遗传学改变:7号染色体改变的可能意义。
Cancer Res. 1987 Dec 15;47(24 Pt 1):6646-52.

人癌细胞系KB的经典多药耐药变体中表皮生长因子受体基因的表达改变。

Altered expression of epidermal growth factor receptor gene in a classical multidrug-resistant variant of a human cancer cell line, KB.

作者信息

Takano H, Kohno K, Shiraishi N, Sato S, Asoh K, Yakushiniji M, Ono M, Kuwano M

机构信息

Department of Biochemistry, Oita Medical School.

出版信息

Jpn J Cancer Res. 1989 Apr;80(4):373-9. doi: 10.1111/j.1349-7006.1989.tb02322.x.

DOI:10.1111/j.1349-7006.1989.tb02322.x
PMID:2501254
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5917741/
Abstract

A variant clone resistant to high doses of colchicine (KB-C1) derived from human cancer KB cell line is resistant to various anticancer agents. The KB-C1 cells were much more resistant to epidermal growth factor and a chimeric toxin, EGF-Pseudomonas exotoxin (PE), than the parental KB cells. KB-C1 cells have decreased numbers of EGF-receptors, though the affinity of the receptors is similar to that in the parental KB cells. A drug-sensitive revertant (C1-R2) partially recovered its EGF-receptor activity. Northern blot analysis showed a decreased level of EGF-receptor mRNA in KB-C1 cells, while the multidrug-resistance gene, mdr-1, was expressed at very high levels in KB-C1 cells, but not in KB or C1-R2 cells. The drug-resistant cells were less tumorigenic than the parental cells when injected into nude mice. A decreased expression of EGF-receptor in these cells may be one of the pleiotropic properties of multidrug-resistant cells and may perhaps represent the basis for their reduced tumorigenicity.

摘要

从人癌KB细胞系衍生而来的对高剂量秋水仙碱具有抗性的变异克隆(KB - C1)对多种抗癌药物具有抗性。与亲本KB细胞相比,KB - C1细胞对表皮生长因子和一种嵌合毒素——表皮生长因子-绿脓杆菌外毒素(PE)具有更强的抗性。KB - C1细胞的表皮生长因子受体数量减少,尽管受体的亲和力与亲本KB细胞中的相似。一种药物敏感回复株(C1 - R2)部分恢复了其表皮生长因子受体活性。Northern印迹分析显示KB - C1细胞中表皮生长因子受体mRNA水平降低,而多药耐药基因mdr - 1在KB - C1细胞中高水平表达,但在KB或C1 - R2细胞中不表达。当将耐药细胞注射到裸鼠体内时,其致瘤性低于亲本细胞。这些细胞中表皮生长因子受体表达的降低可能是多药耐药细胞的多效性特性之一,也许代表了其致瘤性降低的基础。