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Application of polyprezinc in the preparation of drugs for treating castration-resistant prostate cancer

A technology of castration resistance and polyprezinc, which is applied in the field of biomedicine, can solve the problems of drug resistance in CRPC and achieve the effect of shortening the time for clinical transformation

Active Publication Date: 2022-01-07
JIANGNAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, whether it is EPI or Enza, the treatment of CRPC will generally produce drug resistance in about 18 months

Method used

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  • Application of polyprezinc in the preparation of drugs for treating castration-resistant prostate cancer
  • Application of polyprezinc in the preparation of drugs for treating castration-resistant prostate cancer
  • Application of polyprezinc in the preparation of drugs for treating castration-resistant prostate cancer

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1EP

[0029] Embodiment 1EPI, Enza are used for the process that prostate cancer LNCaP cell produces DTP

[0030] EPI, Enza-resistant prostate cancer L-DTP cell lines L-DTP-EPI, L-DTP-Enza have recoverable properties.

[0031] 1. Experimental method:

[0032] LNCaP cells 1x10 6 Each species was planted in a 10cm cell culture dish, and after adhering to the wall on the second day, EPI and Enza were added for 9 days, during which the fresh medium containing the drug was changed every three days; after 9 days, the drug was withdrawn, and the medium was replaced with a fresh medium and placed in the incubator Cells were normally cultured in medium, passaged on day 6, day 12, and day 17, and the cell morphology of DTP (day 9), R5 (day 5 of drug withdrawal), R10, and R20 were photographed under an inverted microscope. After producing DTP and cloned DTP cells, the cells were digested and counted, and the percentage of DTP cells to the total L-parent cells was calculated. L-parent cells ...

Embodiment 2D

[0037] Example 2 Characteristic establishment of AR-related gene expression changes in DTP and Recovery Cell cells

[0038] The cell morphology of DTP cells recovered after 3 passages of drug withdrawal, and the changes in the expression of AR-related genes in the cells could also be restored at this time.

[0039] 1. Experimental method:

[0040] LNCaP cells were placed in a 10cm dish, after overnight adherence to the wall, EPI and Enza were added to treat the cells for 9 days, and then the cells were collected. During this period, the fresh medium added with drugs was replaced every 3 days, and the remaining DTP cells were collected 20 days after drug dispensing. Set LNCaP cells treated with DMSO for 9 days as the NC control group, and treated with EPI and Enza for 9 days to produce drug-resistant cells of L-DTP-EPI and L-DTP-Enza as the treatment group, and the cells of this treatment group after withdrawal of the drug for 20 days were In the recovery group, these three gr...

Embodiment 4

[0049] Example 4 The effect of Enza and Pola combined drug regimen on the C-MYC overexpression prostate cancer mouse model after the continuous drug Enza produces resistance

[0050] Further, in the prostate cancer mouse model, the effect of combined administration of Enza and Pola on relapsed mice after chemical castration (ie continuous administration of Enza) was illustrated.

[0051] 1. Experimental method

[0052] Construct a spontaneous prostate cancer mouse model with C-MYC (Hi-Myc) overexpression. At 4 months, the mice developed mPIN / Cancer transition. At this time, the mice were randomly divided into NC control group (gavage solution), Enza drug After that, Enza was administrated once every three days, and Enza was 10mg / Kg for a total of 30 days. Afterwards, some mice were neck-broken and their prostate cancer was taken to take pictures and weighed. It was found that Enza could significantly alleviate the symptoms. The NC control group was reduced by half, and the re...

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PUM

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Abstract

The invention discloses the application of polyprezinc in the preparation of drugs for treating castration-resistant prostate cancer, and belongs to the technical field of biomedicine. The present invention proposes for the first time a new strategy of using Pola combined with an androgen receptor antagonist to prepare a drug for treating CRPC, and has carried out multi-angle and multi-level verification research. The pharmaceutical composition combined with polyprezinc and androgen receptor of the present invention can be used to treat castration-resistant prostate cancer, and significantly improve the effect of enzalutamide on castration-resistant prostate cancer, realizing the new use of old drugs, It can greatly shorten the time from drug discovery to clinical transformation, and has important clinical significance.

Description

technical field [0001] The invention belongs to the technical field of biomedicine. It specifically relates to the application of polyprezinc in the preparation of drugs for treating castration-resistant prostate cancer. Background technique [0002] Androgen deprivation therapy is the standard treatment for advanced prostate cancer, but patients will eventually develop castration-resistant prostate cancer (CRPC) after an average of 1-3 years of treatment. The so-called CRPC, 2014 CUA guidelines: Prostate cancer with progressive disease after initial continuous androgen deprivation therapy (ADT). The following conditions should be met at the same time: (1) Serum testosterone is maintained at the castration level (<50ng / dL or 1.7nmol / L); (2) Biochemical progress: three consecutive detections of PSA values ​​rising by more than 50% of the lowest value at intervals of one week and The absolute value of the increase is >2ng / ml; or imaging progress: two or more new lesion...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K31/555A61K45/06A61K31/4166A61K31/09A61K31/58A61K31/502A61P35/00
CPCA61K31/555A61K45/06A61K31/4166A61K31/09A61K31/58A61K31/502A61P35/00A61K2300/00
Inventor 陈永泉王荣朱升龙王小英糜远源吴升孙健
Owner JIANGNAN UNIV