Application of cucurbitacin B and analogs thereof in preparation of drugs for treating endometrial cancer
A kind of endometrial cancer, analog technology, applied in the field of medicine
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Embodiment 1
[0019] Inhibitory effect of cucurbitacin B on the autoactivity (phosphorylation) of epithelial growth factor receptor in cultured endometrial carcinoma.
[0020] 1. Human endometrial carcinoma expresses epithelial growth factor receptor.
[0021] experimental method:
[0022] Cell culture:
[0023] Fluorescence real-time quantitative PCR (Real-time PCR)
[0024] Cells were homogenized, RNA was extracted with Trizol, and then reverse-transcribed into cDNA using a kit (TaKaRa Biotechnology, Dalian, China), and amplified using a SYBR Green fluorescent quantitative PCR kit (Agilent Technologies, NC, USA). EGFR and housekeeping gene-actin primers were
[0025] F: 5’-TGATTGGGGATCTTGGAGTTTT-3
[0026] R: 5'-CTTGTGGCTTGTGCTCCTTG-3';
[0027] F: 5’-TGGCACCCAGCACAATGAA-3’
[0028] R: 5'-CTAAGTCATAGTCCGCCTAGAAGCA-3'.
[0029] Prepare 20 μl standard PCR reaction system: 10 μl 2x SYBR green PCR mixture; 0.3 μl 500x ROX dye; 2 μl PCR front-strand primer (10 μM); 2 μl PCR front-stra...
Embodiment 2
[0040] Cucurbitacin B inhibits the activation (phosphorylation) of epithelial growth factor receptors induced by epithelial growth factor in cultured endometrial carcinomas HEC-1-A and HEC-1-B in vitro.
[0041] experimental method:
[0042] Cell culture: Same as above.
[0043] There is no serum in the incubation solution, add 50, 100 and 200 nM cucurbitacin B for 15 minutes, then add epidermal growth factor 10 ng / ml, and detect the activity of epidermal growth factor receptor by immunogel electrophoresis and co-immunoprecipitation after 10 minutes (phosphorylation at Y1173).
[0044] Immunogel electrophoresis and co-immunoprecipitation: same as above.
[0045] see results Figure 4 .
[0046] Experiments have confirmed that cucurbitacin B inhibits the activation of epithelial growth factor receptors caused by epithelial growth factor in human endometrial cancer HEC-1-A and HEC-1-B at concentrations above 50 nM.
Embodiment 4
[0048] Cucurbitacin B inhibited the proliferation of endometrial cancer HEC-1-B cultured in vitro.
[0049] experimental method:
[0050] Cell culture: Same as above.
[0051] MTT method to detect tumor cell growth inhibition rate:
[0052] Tumor cells were seeded in 96-well culture plates, 1 x 10 5 cells / well and incubated overnight to allow them to adhere to the wall.
[0053] Add 200 μl cucurbitacin B incubation solution (0, 50, 100, 200, 400, 800 nM respectively) and continue to incubate for 48 hours, then add 201 MTT (5 mg / mL) and incubate for 4 hours, discard the culture solution, dissolve with 100 lDMSO, Read the absorbance (OD) value A of each well at a wavelength of 570 nm. The culture medium was used instead of drugs as the control group. Calculate the cell inhibition rate according to the A value, and the calculation formula is inhibition rate=[(average A value of the control group-average A value of the blank control group)-(mean A value of the experimental g...
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