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抗Fas单抗和Bcl-2反义脱氧寡核苷酸诱导小儿急性淋巴细胞白血病细胞凋亡的研究 被引量:3

Apoptosis of leukemic cells induced by anti Fas monoclonal antibody and Bcl 2 antisense oligodeoxynucleotides in childhood acute lymphocytic leukemia
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摘要 目的探讨抗Fas单抗、Bcl2反义脱氧寡核苷酸在诱导小儿急性淋巴细胞白血病(简称急淋)细胞凋亡中的作用。方法小儿急淋白血病细胞分别与Bcl2反义脱氧寡核苷酸、抗Fas单抗培养,或与两者一起培养,再分别定量检测其凋亡细胞。结果Bcl2反义脱氧寡核苷酸或抗Fas单抗分别与17例及8例小儿急淋白血病细胞培养48小时后,能各自诱导(35.7±9.4)%及(39.4±8.2)%细胞凋亡。当它们共同作用于8例小儿急淋白血病细胞时可诱导(69.8±13.1)%白血病细胞凋亡。结论Bcl2反义脱氧寡核苷酸与抗Fas单抗均能诱导小儿急淋白血病细胞的凋亡,二者联合应用可显著加强其诱导凋亡的作用。 Objective To explore the function of anti Fas monoclonal antibody (MoAb) and Bcl 2 antisense oligodeoxynucleotides (ASON) in mediating apoptosis of childhood acute lymphocytic leukemia (ALL)cells.Methods The percentage of apoptotic cells was detected after childhood ALL cells were incubated with Bcl 2 ASON, anti Fas MoAb or with both of them, respectively.Results All cells were incubated with Bcl 2 ASON (17 samples) or anti Fas MoAb (8 samples) for 48 hours, and the percentage of apoptotic leukemic cells reached to (35.7±9.4)% and (39.4±8.2)% respectively. The ratio of apoptotic cells from the 8 ALL samples increased to (69.8±13.1)% when they were incubated with both Bcl 2 ASON and anti Fas MoAb.Conclusion The use of both Bcl 2 ASON and anti Fas MoAb may probably provide an effective method for clinical treatment of childhood acute lymphocytic leukemia.
出处 《中华儿科杂志》 CSCD 北大核心 1999年第1期21-23,共3页 Chinese Journal of Pediatrics
基金 国家自然科学基金
关键词 白血病 淋巴细胞性 急性 ASON 单克隆抗体 Apoptosis Antibodies monoclonal Leukemia lymphocytic acute
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  • 1Yang J,Science,1997年,275卷,1129页

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  • 1Okada K, Urano T, Baba H, et al. Independent and differencial expression of two isotypes of human nm23:analysis of the promoter regions of the nm23H1 and nm23H2 genes[J]. Oncogene, 1996,13(9): 1937.
  • 2Hsu JW, Hsu SL, Chu JJ, et al. Increased nm23:MTS1 ratio inverselg correlated with metastasis behaviour in human lung squamous cell carcinoma. Anticancer Res, 1997,17:407 - 411.
  • 3Liotta LA, Steeg PS, Willium G, et al. cancer metastastis and angiogenisis: an imbanance of positive and negative regulation [ J ]. Cell, 1991,64: 327.
  • 4Hochkenbery D, Nunez G, Milliman C, et al. bcl 2 is an inner mitochondrial membrane protein that blocks programmed cell death [ J ] Nature, 1990,348 (6299): 334 - 336.
  • 5Kaiser U, Schilli M, Haag U, et al. Expression of bcl 2 protein in small cell lung cancer[J]. Lung Cancer,1996,15( 1 ) :31 - 40.
  • 6Heming G V, Guinee D G, Chu W S, et al. bcl - 2 immunohistochemistry in a surgical series of non - small cell lung cancer patients [J ]. Am J Emergency Med, 1998, 29(1):60.
  • 7Steeg PS, Bevilacqua G, Kopper L, et al. Evidence for a novel gene associated with low tumor metastastic potential[J]. Natil Cancer Inst, 1998,80(3) :200-204.
  • 8Yang E,Korsmeyer S.Molecular thanatopsis:a discourse on the bcl-2 family and cell death[J].Blood,1996,88(2):388-401.
  • 9Vaux D,Cory S,Fulcu M,et al.Effects of bcl-2 gene in the tumour cell culture in vitro[J].Nature,1998,335(6):440.
  • 10Ziegler A,Luedke GH,Fabbro D,et al.Induction of apoptosis in small-cell lung cancer cell by an antisense oligodeoxynucleotide targeting the bcl-2 coding sequence[J].J Natil Cancer Institute,1997,89(14):1027-1036.

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