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Study on antisense oligoncleotides as inhibitor of human acute promyelocytic leukemia proliferation and protein expression / 中国新药与临床杂志
Chinese Journal of New Drugs and Clinical Remedies ; (12): 174-176, 2001.
Article in Chinese | WPRIM | ID: wpr-410978
ABSTRACT

AIM:

To study on antisense oligoncleotides as inhibitor of human acute promyelocytic leukemia (HL-60) proliferation and C-myc protein expression.  

METHODS:

Oligonucleotides with different lengths (18-21 mer) complementary to the definite regions of C-myc mRNA, modified groups (with S replaced O in internucleotide phosphate linkage) and unmodified ones (with natural internucleotide phosphate linkage) were designed and synthesized. These olignucleotides were tested for their activity on HL-60 cell and also for their toxicity on normal lymphatic cells of human.  

RESULTS:

It was found that two of the oligonucleotides complementary to 5′-44-61 and 5′-556-576 the regions of C-myc mRNA exhibited great inhibitory effects (59.5 % and 62.7 %) on growth of HL-60 cells for a definite time. And no toxicity of the two antisense oligonucleotides was found on normal lymphatic cells of human.  

CONCLUSION:

The sequence of antisense oligonucleotides complementary to 5′-44-61 of C-myc mRNA was designed newly by us may be turned into inhibitory medicine of HL-60 cells.
Full text: Available Index: WPRIM (Western Pacific) Language: Chinese Journal: Chinese Journal of New Drugs and Clinical Remedies Year: 2001 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Language: Chinese Journal: Chinese Journal of New Drugs and Clinical Remedies Year: 2001 Type: Article