CN109172571B - Application of alkaloid in reversing drug resistance of cisplatin in lung cancer - Google Patents
Application of alkaloid in reversing drug resistance of cisplatin in lung cancer Download PDFInfo
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- CN109172571B CN109172571B CN201811069714.2A CN201811069714A CN109172571B CN 109172571 B CN109172571 B CN 109172571B CN 201811069714 A CN201811069714 A CN 201811069714A CN 109172571 B CN109172571 B CN 109172571B
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/439—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom the ring forming part of a bridged ring system, e.g. quinuclidine
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Abstract
The invention discloses an application of alkaloid in reversing drug resistance of lung cancer cisplatin. Cisplatin (DDP) is a first-line chemotherapeutic drug after lung cancer operation, and natural and acquired drug resistance limits combined chemotherapy curative effect based on cisplatin. Therefore, there is a need to develop drugs that reverse the resistance of cisplatin in lung cancer. The invention discovers that compounds TA-1, TA-2, TB-1, TB-2, TB-3, TC-1, TD-1, TE-1 and TE-2 can effectively reverse the drug resistance of lung cancer cells to cisplatin, wherein TC-1 and TD-1 not only can reverse the drug resistance, but also can enhance the sensitivity of the lung cancer cells to the cisplatin. Compound TB-4 did not have this effect.
Description
Technical Field
The invention belongs to the field of medicines, and relates to an application of alkaloid in reversing drug resistance of lung cancer cisplatin.
Background
Lung cancer is the most common malignant tumor of respiratory system, and the incidence and mortality of lung cancer are the first of the malignant tumors and have a tendency to rise year by year. From a clinical perspective, lung cancer is generally classified into two categories, combining histological and biological characteristics of tumor cells: small Cell Lung Cancer (SCLC) and non-small cell lung cancer (NSCLC), with about 85% of lung cancers being NSCLC. NSCLC is prone to regional lymph node metastasis and blood-borne dissemination, and the prognosis of patients is poor, and the 5-year survival rate is less than 15%.
Cisplatin (DDP) is a first-line chemotherapeutic drug after lung cancer operation, and natural and acquired drug resistance limits combined chemotherapy curative effect based on cisplatin. Therefore, there is a need to develop drugs that reverse the resistance of cisplatin in lung cancer.
Disclosure of Invention
The invention aims to overcome the defects of the prior art and provides the application of alkaloid in reversing the drug resistance of lung cancer cisplatin.
The above purpose of the invention is realized by the following technical scheme:
the application of the alkaloid with the following structure in the preparation of the medicine for reversing the cisplatin resistance of the lung cancer patient:
A pharmaceutical preparation for reversing drug resistance of cisplatin in lung cancer patients comprises the above alkaloids as active ingredients, and pharmaceutically acceptable adjuvants.
The application of the alkaloid with the following structure in the preparation of the medicine for reversing the cisplatin resistance of the lung cancer patient:
A pharmaceutical preparation for reversing drug resistance of cisplatin in lung cancer patients comprises the above alkaloids as active ingredients, and pharmaceutically acceptable adjuvants.
The application of the alkaloid with the following structure in the preparation of the medicine for reversing the cisplatin resistance of the lung cancer patient:
A pharmaceutical preparation for reversing drug resistance of cisplatin in lung cancer patients comprises the above alkaloids as active ingredients, and pharmaceutically acceptable adjuvants.
The application of the alkaloid with the following structure in the preparation of the medicine for reversing the cisplatin resistance of the lung cancer patient:
A pharmaceutical preparation for reversing drug resistance of cisplatin in lung cancer patients comprises the above alkaloids as active ingredients, and pharmaceutically acceptable adjuvants.
The application of the alkaloid with the following structure in the preparation of the medicine for reversing the cisplatin resistance of the lung cancer patient:
A pharmaceutical preparation for reversing drug resistance of cisplatin in lung cancer patients comprises the above alkaloids as active ingredients, and pharmaceutically acceptable adjuvants.
Has the advantages that:
the invention discovers that compounds TA-1, TA-2, TB-1, TB-2, TB-3, TC-1, TD-1, TE-1 and TE-2 can effectively reverse the drug resistance of lung cancer cells to cisplatin, wherein TC-1 and TD-1 not only can reverse the drug resistance, but also can enhance the sensitivity of the lung cancer cells to the cisplatin. Compound TB-4 did not have this effect.
Drawings
FIG. 1 shows the half inhibitory concentration IC50 values of cisplatin for each group of cells.
Detailed Description
The following detailed description of the present invention will be made with reference to the accompanying drawings and examples, but should not be construed to limit the scope of the present invention.
First, experimental material
The alkaloids to be researched and tested are prepared according to the conventional method and the literature method, and are divided into five main groups according to chemical structures, and the specific chemical structures and the numbers are shown in the following table.
Lung cancer cell line H460 was purchased from ATCC, DMEM medium, and fetal bovine serum from GIBCO.
Second, Experimental methods
1. Cell culture
After conventional recovery of human lung cancer cell line H460, DMEM medium containing 10% FBS, 50U/ml streptomycin, 50U/ml penicillin and 4mmol/L L-glutamine at 37 deg.C and 5% CO2Culturing under the condition, and changing the culture solution every 2-3 days.
2. Construction of cisplatin-resistant Strain H460/DDP
The human lung cancer cisplatin-resistant cell strain H460/DDP is established by a cisplatin continuous contact concentration increasing induction method.
The specific method comprises the following steps: culturing H460 cells in a logarithmic growth phase by using DMEM with cisplatin concentration of 0.1 mug/ml, digesting and passaging the cells after 4 weeks, culturing by using normal full culture, increasing the cisplatin concentration to 0.2 mug/ml after the cells adhere to the wall, continuously culturing for 4 weeks, and digesting and passaging; then the concentration of cisplatin is increased to 0.5, 1.0 and 2.0 mug/ml in sequence, and the lung cancer cisplatin resistant strain H460/DDP is obtained after continuous culture for 5 months.
3. Grouping and administration of drugs
Administration group: H460/DDP cells in logarithmic growth phase were seeded at 1000/well in 96-well plates at 37 ℃ with 5% CO2Culturing in an incubator. After the cells adhere to the wall, adding complete culture media containing 5 mu M of TA-1, TA-2, TB-1, TB-2, TB-3, TB-4, TC-1, TD-1, TE-1 or TE-2(DMSO is a solvent) respectively for culture;
H460/DDP group: H460/DDP cells, only adding an equivalent solvent DMSO, not adding a medicine, and other administration groups;
h460 group: h460 cells, the same amount of the vehicle DMSO only, no drug, other same dosing groups.
4. Determination of sensitivity of various groups of cells to cisplatin
Culturing each group of cells for 48h, discarding the old culture medium, and addingGradient concentration cisplatin, each concentration setting 3 multiple holes, 37 degrees C, 5% CO2After culturing for 48h in the incubator, the old culture medium is discarded, a fresh culture medium containing 10% CCK-8 is added, incubation is carried out for 3h at 37 ℃, the optical density value at 450nm is measured, and the half inhibition concentration IC50 is calculated.
5. Data processing
Statistical analysis was performed using SPSS 17.0, data were expressed as mean. + -. standard deviation, and comparisons between groups using Student's t test were statistically significant for differences P < 0.05.
Third, experimental results
The median inhibitory concentration IC50 values for cisplatin for each group of cells are shown in table 1 and figure 1. Compared with the H460 group, the IC50 value of the lung cancer cells of the H460/DDP group is obviously increased (P is less than 0.05), which indicates that the H460/DDP lung cancer cells generate obvious resistance to cis-platinum; compared with the H460/DDP group, the IC50 values of the lung cancer cells of the TA-1, TA-2, TB-1, TB-2, TB-3, TC-1, TD-1, TE-1 and TE-2 groups are obviously reduced (P is less than 0.05), which indicates that the sensitivity of the H460/DDP lung cancer cells to cis-platinum is enhanced by the incubation of the TA-1, TA-2, TB-1, TB-2, TB-3, TC-1, TD-1, TE-1 and TE-2 (P is less than 0.05).
The effect of the compound TB-4 is not obvious (P is more than 0.05).
TABLE 1 half inhibitory concentration IC50 values of cisplatin for each group of cells
| Group of | IC50 value (μ g/ml) | Group of | IC50 value (μ g/ml) |
| H460 group | 14.21±1.25 | TB-3 administrationMedicine group | 20.06±1.19 |
| H460/DDP group | 52.85±1.63 | TB-4 administration group | 48.72±1.55 |
| TA-1 administration group | 21.07±1.47 | TC-1 administration group | 7.61±0.93 |
| TA-2 administration group | 23.42±1.38 | TD-1 administration group | 7.33±0.88 |
| TB-1 administration group | 18.95±1.10 | TE-1 administration group | 15.62±1.27 |
| TB-2 administration group | 17.18±1.08 | TE-2 administration group | 9.24±0.96 |
The experimental results show that the compounds TA-1, TA-2, TB-1, TB-2, TB-3, TC-1, TD-1, TE-1 and TE-2 can effectively reverse the drug resistance of the lung cancer cells to the cisplatin, wherein the TC-1 and the TD-1 not only can reverse the drug resistance, but also can enhance the sensitivity of the lung cancer cells to the cisplatin. Compound TB-4 did not have this effect.
The purpose of the foregoing embodiments is to present some concepts of the invention in a detailed description, but it is not intended to limit the scope of the invention to the specific embodiments described.
Claims (1)
1. The application of the alkaloid with the following structure in preparing the medicine for treating the cisplatin-resistant lung cancer patient comprises the following steps:
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Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102008475A (en) * | 2010-09-09 | 2011-04-13 | 汕头大学医学院 | Application of quinolizidine in preparing tumor treatment drugs |
| CN103509021A (en) * | 2012-06-21 | 2014-01-15 | 上海药明康德新药开发有限公司 | Cytisine derivative, its preparation method and anticancer effect research |
| CN106913571A (en) * | 2017-04-19 | 2017-07-04 | 山西大学 | A kind of medicine and its application for treating tumour |
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Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102008475A (en) * | 2010-09-09 | 2011-04-13 | 汕头大学医学院 | Application of quinolizidine in preparing tumor treatment drugs |
| CN103509021A (en) * | 2012-06-21 | 2014-01-15 | 上海药明康德新药开发有限公司 | Cytisine derivative, its preparation method and anticancer effect research |
| CN106913571A (en) * | 2017-04-19 | 2017-07-04 | 山西大学 | A kind of medicine and its application for treating tumour |
Non-Patent Citations (2)
| Title |
|---|
| Cytisine induces endoplasmic reticulum stress caused by calcium overload in HepG2 cells;LEI YU et al;《ONCOLOGY REPORTS》;20180331;第39卷(第3期);全文 * |
| 浙贝母总生物碱对人肺腺癌A549/ 顺铂细胞耐药性的逆转作用;李泽慧等;《中国药理学与毒理学杂志》;20130630;第27卷(第3期);全文 * |
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