Method for overcoming reverse tolerance of tumors
An anti-tumor drug and tumor technology, applied in the field of biomedicine, can solve the problems of difficult to achieve effective reversal concentration, low drug utilization rate, poor targeting, etc., and achieve the effects of simple and easy acquisition, simple nutritional requirements, and easy control.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2020-02-07
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Abstract
Description
technical field
[0001] The invention belongs to the field of biomedicine, and in particular relates to a method for overcoming tumor drug resistance. Background technique
[0002] Chemotherapy is one of the main methods for treating malignant tumors. The biggest advantage of chemotherapy compared with surgery and radiotherapy is that chemotherapy is a systemic treatment. Chemotherapy drugs can reach the whole body through the human circulatory system through oral administration, injection, etc., so they have a killing effect on primary cancer lesions, metastatic lesions, and even free circulating tumor cells. Through natural extraction, artificial synthesis and a large number of screening, many drugs have been approved by the US Food and Drug Administration for clinical application. At present, common chemotherapy drugs include adriamycin, 5-fluorouracil, camptothecin, paclitaxel, and etoposide. , Cismolybdenum, etc. However, while chemotherapy drugs kill tumor cells, they...
Examples
Embodiment
[0029] Prepare for the experiment: Prepare a 500ml Erlenmeyer flask, pour cyanobacteria and sterilized BG11 medium into the aseptic operating table, seal the bottle mouth with a breathable parafilm, and place it in the sun for cultivation and amplification.
[0030] Experiment 1: Increased oxygenation in vitro to increase the entry of doxorubicin into cells
[0031]Spread hypoxic breast cancer cells (MCF-7) and normal state breast cancer cells (MCF-7) into the confocal dish and put them into the incubator (the hypoxic cells are placed in the hypoxic incubator, the normal state The cells were cultured in a normal incubator) for 24 hours, and the cells in the hypoxic state were added with 2×10 7 cfu / mL cyanobacteria or no cyanobacteria, 660nm laser irradiation or no laser irradiation and culture for 24 hours, add DOX for co-incubation for 1 hour, stain the nucleus, and shoot confocal.
[0032] Confocal results such as figure 1 As shown, the cyanobacteria and laser irradiation ...