Multi-medicine medicine-resistant RNA interference medicine for resisting tumor
A technology of RNA interference and multi-drug resistance, applied in the direction of anti-tumor drugs, DNA/RNA fragments, drug combinations, etc., can solve problems such as adverse reactions, high toxicity, and limited clinical application
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Embodiment 1
[0047] After K562 / A02 cells were treated with siRNA for 24 hours, the expression of mRNA in the si-mdr1 group was down-regulated by (17.23±2.47)% (p>0.05) compared with the negative control group, and mdr- 1 mRNA expression was significantly reduced, respectively (38±1.23)% and (58±1.54)% (pfigure 1 .
Embodiment 2
[0048] Example 2. P-gp expression detection
[0049] After 48 hours of siRNA action, flow cytometry showed that the three groups inhibited the expression of p170 to varying degrees, and the positive rate of p170 expression in the si-mdr1 action group decreased from (76.0±1.03)% before treatment to (56.72±1.03)% after treatment. 1.41)%, the si-mdr2 effect group decreased to (42.70±1.17)% (p0.05), see figure 2 .
[0050] Changes in drug sensitivity of K562 / A02 cells after RNAi treatment: IC 50 Refers to the concentration of chemotherapeutic drugs when the cell inhibition rate is 50%. It can be seen from Table 1 that after the action of si-mdr2 and si-mdr3, the sensitivity of K562 / A02 to the chemotherapeutic drug ADM increases, suggesting that RNAi can restore the sensitivity of K562 / A02 to chemotherapeutic drugs. sensitivity. Example 3. Reversal effect of siRNA on drug resistance of K562 / A02 cells
Embodiment 3
[0050] Changes in drug sensitivity of K562 / A02 cells after RNAi treatment: IC 50 Refers to the concentration of chemotherapeutic drugs when the cell inhibition rate is 50%. It can be seen from Table 1 that after the action of si-mdr2 and si-mdr3, the sensitivity of K562 / A02 to the chemotherapeutic drug ADM increases, suggesting that RNAi can restore the sensitivity of K562 / A02 to chemotherapeutic drugs. sensitivity. Example 3. Reversal effect of siRNA on drug resistance of K562 / A02 cells
[0051] Table 1 compares the results of siRNA reversal of drug resistance in K562 / A02 cells. Each experiment was repeated 3 times, with 3 parallel wells each time, and the average value was taken. si-mdr1, si-mdr2 and si-mdr3 all have multidrug resistance reversing effects, and si-mdr3 has the most significant effect.
[0052] Table 1
[0053] IC 50 (μg / ml) relative reversal efficiency
[0054] (%)
[0055] K562 0.05 /
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