Application of bcl-xl inhibitor and oncolytic virus in the preparation of antitumor drugs
一种溶瘤病毒、抑制剂的技术,应用在生物医药领域,达到增加抗肿瘤效应、增强抑制作用、提高治疗有效性的效果
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Embodiment 1
[0049] Example 1 ABT-263 and M1 virus significantly increase the morphological lesions of human hepatocellular carcinoma lines
[0050] Material:
[0051] Human hepatocellular carcinoma Hep3B, M1 virus, high glucose DMEM medium, inverted phase contrast microscope.
[0052] method:
[0053] a) Cell culture: Human hepatocellular carcinoma Hep3B was grown in DMEM complete medium containing 10% FBS, 100 U / ml penicillin and 0.1 mg / ml streptomycin; all cell lines were placed in 5% CO 2 , cultured and subcultured in a closed incubator with a constant temperature of 37°C (95% relative humidity), and observed the growth with an inverted microscope. The cells were subcultured every 2-3 days, and the cells in the logarithmic growth phase were taken for formal experiments.
[0054] b) Cell treatment and morphological observation: cells in the logarithmic growth phase were selected, and DMEM complete culture medium (containing 10% fetal bovine serum, 1% double antibody) was used to make...
Embodiment 2
[0057] Example 2 Combined treatment of ABT-263 or ABT-737 with M1 virus significantly reduces the survival rate of human cancer cell lines
[0058] Material:
[0059] Human hepatocellular carcinoma Hep3B, human bladder carcinoma T24, human colorectal carcinoma LoVo, M1 virus, high glucose DMEM medium, automatic enzyme-linked detection microplate reader.
[0060] method:
[0061] a) Cell inoculation, administration treatment: select logarithmic growth phase cells, DMEM complete culture medium (containing 10% fetal bovine serum, 1% double antibody) make cell suspension, with 4 × 10 3 The density per well was seeded in a 96-well culture plate. After 12 hours, the cells were completely attached to the wall. The experiment was divided into control group, ABT-263 alone group, M1 infection group and ABT-263 / M1 combination group or ABT-737 / M1 combination group. The dose used is: M1 virus infects cells; different dose gradients are set for M1 virus.
[0062] b) Reaction of MTT with...
Embodiment 3
[0067] Example 3 Inhibition of Bcl-xL synergistic anti-tumor effect of M1 oncolytic virus
[0068] Material:
[0069] M1 virus, human liver cancer cell Hep3B, bladder cancer cell T24, Bcl-xL and Bcl-w RNA interference fragments, MTT (methyl azolium blue), phase contrast microscope.
[0070] Bcl-xL interference fragment (Si RNA):
[0071] Sense strand (SEQ ID NO.1)
[0072] 5'-GGAUACAGCUGGAGUCAGUdTdT-3'
[0073] Antisense strand (SEQ ID NO.2)
[0074] 5'-ACUGACUCCAGCUGUAUCCdTdT-3';
[0075] Bcl-w interference fragment (Si RNA):
[0076] Sense strand (SEQ ID NO.3)
[0077] 5'-CAGCUGUAUUCCAUUACAUdTdT-3'
[0078] Antisense strand (SEQ ID NO.4)
[0079] 5'-AUCUAAUGGAAUACAGCUGdTdT-3'
[0080] method:
[0081] Select the cells in the logarithmic growth phase, prepare the cell suspension with DMEM complete culture medium, and use 1×10 5 seeded in 6-well plates. After 24 hours, add liposome-encapsulated Si RNA target gene fragments and infect M1 virus 24 hours later. 48 ho...
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