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K562/ADM耐药细胞株的建立及其生物学特性的初步观察 被引量:18

ESTABLISHMENT QF K562 CELL LINE RESISTANT TO ADM AND A PRELIMINARY OBSERVATION ON ITS CHARACTERISTIC BLOLOGY
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摘要 我们建立的K562/ADM耐药细胞株,在ADM浓度为2.4μg/m1(4.46μM)中已稳定培养3.5个月,传了30—35代,K562/ADM亦具有多药耐受件(Multidrug Resistance,MDR)的特点,对ADM、VCR、AT—1258和DDP的耐受性分别为K562的114.7、94.0、13.3和7.4倍,但对5—FU不产生交叉耐药。K562和K562/ADM的倍增时间分别为19.2h和52.8h,集落生成率分别为37.5%和11.1%,K562染色体数为34—68,中位数为56;K562/MDM染色体数为32—90,中位数为50,K562/ADM可做为耐药机理和克服耐药措施研究的极好模型。 A K 562 cell line resistant to ADM was established by cultivation in increasing concentration of ADM. It has been growing for 30-35 generation in 3.5 months in a medium containing 2.4μg/ml (4.46μM). It was characterized with multidrug resistance(MDR), and its resistance to ADM, VCR, AT-1258 and DDP, were 114.7, 94.0, 13.3, and 7.4 time as compared with normal K562 cell line, but with no cross-resistance to 5-Fu. The doubling times of K562 and K562/ADM were 19.2 hr. and 52.8 hr., and rates of colony formation of them, 37.5% and 11.1% respectively Numbers of chromosome and median of K562 were 34-68 and 56 respectively, and K562/ADM, 32-90 and 50. K562 cell line resistant to ADM may be used as a model for the study of mechanism and reverse method of anticancer-drug resistance.
出处 《癌症》 SCIE CAS CSCD 北大核心 1992年第3期222-224,共3页 Chinese Journal of Cancer
关键词 K562 K562/ADM 耐药细胞株 生物学 K562 K562/ADM IC50 doubling times
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  • 1李昆霖,吴国明,戢福云,徐智,黄桂君.人小细胞肺癌多药耐药细胞差异表达基因的克隆研究[J].第三军医大学学报,2006,28(24):2403-2405. 被引量:5
  • 2Tanaka M, Inase N, Miyake S, et al. Neuron specific enolase prorooter for suicide gene therapy in small cell lung carcinom[ J]. Anticancer Res ,2001,21 (1A) : 291 -294.
  • 3Scheffer GL, Scheper R.I. Drug resistance molecules: lessons from oncology[J]. Novartis Found Symp, 2002, 243 : 19 -31.
  • 4Damian D, Michelutti A. P - glycoprotein, lung resistance - related protein and multidrug resistance -associated protein in de novo adult acute lymphoblastic leukaemia [ J ]. Br J Haematol, 2002, 116(3) :519 -527.
  • 5Ryu JS, Hong YC, Han HS, et al. Association between polymorphisms of ERCC1 and XPD and survival in non - small - cell lung cancer patients treated with cisplatin combination chemotherapy [J]. Lung Cancer, 2004 ,44-(3) :311 -316.
  • 6Okouoyo S, Herzer K, Ucur E, et al. Rescue of death receptor and mitochondrial apoptosis signaling in resistant human NSCLC in vivo [ J ]. Int J Cancer, 2004,108 (4) :580 - 587.
  • 7Castro A, Jerez MJ, Gil C, et al. Cyclic nucleotide phosphodiesterases and their role in immunomodulatory responses: advances in the development of specific phosphodiesterase inhibitors [ J ]. Med Res Rev, 2005, 25 ( 2 ) : 229 - 244.
  • 8Ahlstrom M, Pekkinen M, Huttunen M, et al. Dexamethasone down - regulates cAMP - phosphodiesterase in human osteosarcoma cells[J]. Biochem Pharmacol, 2005, 69(2) : 267 -275.
  • 9Ding YH, Ellenberger T. Structural determinants for inhibitor specificity and selectivity in PDE2A using the wheat germ in vitro translation system [ J ]. Biochemistry, 2005, 44 ( 23 ) : 8312 - 8325.
  • 10Rosman GJ, Martins TJ, Sonnenburg WK, et al. Isolation and characterization of human cDNAs encoding a cGMP - stimulated 3',5'- cyclic nucleotide phosphodiesterase[ J]. Gene, 1997, 191 ( 1 ) :89 -95.

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