Inhibition of Leukemia Cell Proliferation using c-myb Antisense Oligonucleotides

Ediz DEMİRPENÇE

Makale detayları

Inhibition of Leukemia Cell Proliferation using c-myb Antisense Oligonucleotides

Yazarlar:

Ediz DEMİRPENÇE

Yayıncı:

TUBITAK

Dergi:

Turkish Journal of Medical Sciences 2002 Vol.32 Issue 5, pp.369-372

Belge Tipi:

Makale

Yayın Tarihi:

4/2002

Belge Dili:

Türkçe

Document ID (Org No.):

2000756891

Sıklık:

İki Aylık

eISSN:

1303-6165

pISSN:

1300-0144

Anahtar kelimeler:

Özet:

 

Antisense oligodeoxynucleotides (AS-ODNs) are short DNA sequences synthesized complementary to the mRNA and they inhibit the expression of the target gene by forming a mRNA-DNA duplex. This strategy can be considered to be an alternative therapy for cancers characterized by amplified oncogene activity.  The purpose of this study was to evaluate the inhibitory effect of AS-ODNs on two human leukemia cell lines (HL-60 and K562). Cells were treated with c-myb AS-ODNs at two different concentrations and cell proliferation was monitored on the 5th and 7th days of culture. Sense and scrambled ODNs were used as the control.  In both cell lines, AS-ODNs inhibited cell proliferation up to 90%, with inhibition being more important at high ODN concentration. A slight inhibition was also observed with sense ODNs after 5 days of culture; but in contrast with the AS-ODNs, this inhibition was diminished in 7 days. Scrambled ODNs caused a higher inhibition than sense ODNs.  This study shows that AS-ODNs, targeted to an oncogene involved in cell proliferation, inhibit malignant cell proliferation. The inhibition observed with sense or scrambled ODNs is due to non-sequence-specific ODN binding. However, these non-specific effects decrease at longer incubation times whereas the antisense effect persists.

 

Antisense oligodeoxynucleotides (AS-ODNs) are short DNA sequences synthesized complementary to the mRNA and they inhibit the expression of the target gene by forming a mRNA-DNA duplex. This strategy can be considered to be an alternative therapy for cancers characterized by amplified oncogene activity.  The purpose of this study was to evaluate the inhibitory effect of AS-ODNs on two human leukemia cell lines (HL-60 and K562). Cells were treated with c-myb AS-ODNs at two different concentrations and cell proliferation was monitored on the 5th and 7th days of culture. Sense and scrambled ODNs were used as the control.  In both cell lines, AS-ODNs inhibited cell proliferation up to 90%, with inhibition being more important at high ODN concentration. A slight inhibition was also observed with sense ODNs after 5 days of culture; but in contrast with the AS-ODNs, this inhibition was diminished in 7 days. Scrambled ODNs caused a higher inhibition than sense ODNs.  This study shows that AS-ODNs, targeted to an oncogene involved in cell proliferation, inhibit malignant cell proliferation. The inhibition observed with sense or scrambled ODNs is due to non-sequence-specific ODN binding. However, these non-specific effects decrease at longer incubation times whereas the antisense effect persists.

Makale detayları

Inhibition of Leukemia Cell Proliferation using c-myb Antisense Oligonucleotides

Yazarlar:

Ediz DEMİRPENÇE

Yayıncı:

TUBITAK

Dergi:

Turkish Journal of Medical Sciences 2002 Vol.32 Issue 5, pp.369-372

Belge Tipi:

Makale

Yayın Tarihi:

4/2002

Belge Dili:

Türkçe

Document ID (Org No.):

2000756891

Sıklık:

İki Aylık

eISSN:

1303-6165

pISSN:

1300-0144

Gene therapy

antisense oligonucleotides

c-myb

leukemia

Sayı

Makale detayları

Inhibition of Leukemia Cell Proliferation using c-myb Antisense Oligonucleotides

Yazarlar: Ediz DEMİRPENÇE

Yayıncı: TUBITAK

Dergi: Turkish Journal of Medical Sciences 2002 Vol.32 Issue 5, pp.369-372

Belge Tipi: Makale

Yayın Tarihi: 4/2002

Belge Dili: Türkçe

Document ID (Org No.): 2000756891

Sıklık: İki Aylık

eISSN: 1303-6165

pISSN: 1300-0144

Gene therapy

antisense oligonucleotides

c-myb

leukemia

Sayı

Yazarlar:

Ediz DEMİRPENÇE

Yayıncı:

TUBITAK

Dergi:

Turkish Journal of Medical Sciences 2002 Vol.32 Issue 5, pp.369-372

Belge Tipi:

Makale

Yayın Tarihi:

4/2002

Belge Dili:

Türkçe

Document ID (Org No.):

2000756891

Sıklık:

İki Aylık

eISSN:

1303-6165

pISSN:

1300-0144