New use of natural abscisic acid i preparing tumour cell
A technology of natural abscisic acid and differentiation inducer, applied in the field of natural substances, can solve the problems of limited development and application, toxic and side effects, and achieve the effects of inhibiting the growth of cancer cells and tumors, with less toxic and side effects, and simple operation.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0017] Example 1: Study on the differentiation induction of prostate cancer cells by natural abscisic acid:
[0018] The prostate cancer DU-145 cells in the logarithmic growth phase were divided into two groups, the experimental group and the control group, and the experimental group was added with 20ul2×10 -2 g / L ABA (dissolved in absolute ethanol), make the final concentration of ABA in the nutrient solution be 10 -2 g / L, the control group was added with 20ul of absolute ethanol, the concentration of calf serum in the culture solution was 130mI / L, and the cells were cultured by conventional methods. Routinely change culture medium after adding medicine 48h, maintain identical drug concentration (ABA concentration is 10 -2 g / L). During the culture process, the morphological changes of DU-145 cells were dynamically observed with an inverted optical microscope.
[0019] result:
[0020] Observation of cell morphology and ultrastructure: DU-145 cells cultured and treated wit...
Embodiment 2
[0023] Example 2: Study on the differentiation induction of promyelocytic leukemia HL-60 cells by natural abscisic acid:
[0024] The promyelocytic leukemia HL-60 cells in the logarithmic growth phase were divided into the experimental group and the control group, and the experimental group was added with 10ul 5×10 -1 g / L ABA (dissolved in absolute ethanol), so that the final concentration of ABA in the culture medium was 1×10 -1 g / L, the control group was added with 10ul of absolute ethanol, the concentration of calf serum in the culture solution was 130mI / L, and the cells were cultured by conventional methods. After adding the drug for 48 hours, the culture medium was routinely replaced to maintain the same drug concentration (the concentration of ABA was 1×10 -1 g / L). During the culture process, the morphological changes of HL-60 cells were dynamically observed by transmission electron microscope.
[0025] Observation of cell morphology and ultrastructure: HL-60 cells cu...
Embodiment 3
[0030]3. Effect of natural abscisic acid on the ability of xenograft tumor formation in nude mice
[0031] 1).Material
[0032] (1) 3-week-old Balb / c.nu nude mice, with an average body weight of about 20 g, are all male.
[0033] (2) Barrier system for SPF rearing of nude mice.
[0034] (3) Human oral cancer Tca8113 cell line 2.
[0035] 2) method
[0036] 2.1) Preparation of inoculated cells
[0037] Cultivate Tca8113 cells to the logarithmic growth phase according to the method of test 1, detach and disperse the adherent tumor cells with digestive solution, wash them twice with serum-free culture medium, count the viable cells, and adjust to 2 with PBS solution. ×10 7 / ml cell suspension. Use a syringe with a No. 6 needle to draw an appropriate amount of tumor cell suspension to inoculate nude mice. Each animal is inoculated to one site (inoculated in the armpit of nude mice), and each site is injected with 0.2ml of tumor cell suspension, containing 4 live cells. ×10 ...
PUM

Abstract
Description
Claims
Application Information

- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com