Use of enoph1 in the treatment and / or diagnosis of cardiomyopathy or heart failure

By overexpressing Enoph1 in body fluids, cells, or tissues, or by detecting the expression level of Enoph1, the problems of treatment and diagnosis of cardiomyopathy and heart failure have been solved, enabling effective treatment and diagnosis of cardiomyopathy and heart failure.

CN122168744APending Publication Date: 2026-06-09GENERAL HOSPITAL OF PLA

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
GENERAL HOSPITAL OF PLA
Filing Date
2026-03-30
Publication Date
2026-06-09

AI Technical Summary

Technical Problem

Existing technologies have not effectively utilized Enoph1 in the treatment and diagnosis of cardiomyopathy and heart failure, especially in the treatment and diagnosis of heart failure with reduced ejection fraction and septic cardiomyopathy.

Method used

The diagnosis and treatment of cardiomyopathy or heart failure can be achieved by overexpressing Enoph1 or using Enoph1 as a biomarker, by using a vector or Enoph1 protein agonist to overexpress Enoph1 in body fluids, cells or tissues, or by detecting the expression level of Enoph1 gene mRNA or protein.

Benefits of technology

It has achieved effective treatment of cardiomyopathy and heart failure, improved patient survival rate, reversed myocardial cell damage, restored myocardial cell function, and improved diagnostic efficacy.

✦ Generated by Eureka AI based on patent content.

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Abstract

The application relates to the field of biological medicine, and particularly relates to application of Enoph1 in treatment and / or diagnosis of cardiomyopathy or heart failure. The application finds that the expression level of Enoph1 in patients with cardiomyopathy or heart failure is significantly up-regulated. Further, by overexpressing Enoph1 in myocardial cells, it is found that overexpression of Enoph1 can restore the number of myocardial cells, glycolysis, oxygen respiration function, mitochondrial function of the myocardial cells and reduce generation of active oxygen, protect the myocardial cells, and achieve the effect of treating cardiomyopathy or heart failure.
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Claims

1. Application of Enoph1 in the preparation of products for the diagnosis, early warning, treatment and / or prevention of cardiomyopathy or heart failure.

2. The application according to claim 1, characterized in that, The products described for the treatment and / or prevention of cardiomyopathy or heart failure include reagents that express or overexpress Enoph1; Preferably, the reagent includes one or more of a vector, a factor that promotes Enoph1 gene transcription, or an Enoph1 protein agonist.

3. The application according to claim 1, characterized in that, The products described for diagnosing and / or providing early warning of cardiomyopathy or heart failure include reagents for detecting the expression level or concentration of Enoph1 gene mRNA or its protein. Preferably, the reagents include one or more of the following: reagents required for reverse transcription, reagents required for PCR, reagents required for BCA method, reagents required for Western blotting method, reagents required for sequencing, or reagents required for mass spectrometry.

4. The application according to any one of claims 1-3, characterized in that, The Enoph1 mentioned includes one or more Enoph1s derived from body fluids, cells, tissues or organs; Preferably, the bodily fluid includes blood; Preferably, the cells, organs, or tissues include those derived from the heart.

5. The application according to any one of claims 1-4, characterized in that, The cardiomyopathy described is septic cardiomyopathy; Preferably, the heart failure is heart failure with reduced ejection fraction.

6. Application of Enoph1 overexpression in the preparation of products for the treatment and / or prevention of cardiomyopathy or heart failure.

7. Application of Enoph1 as a biomarker in the preparation of products for the diagnosis and / or early warning of cardiomyopathy or heart failure.

8. A method for constructing a cardiomyocyte injury model, characterized in that, The construction method described includes knocking out or knocking down Enoph1 in cardiomyocytes; Preferably, the construction method includes using siRNA.

9. The construction method according to claim 8, characterized in that, The target sites of the siRNA include SEQ ID NO: 1-3, preferably SEQ ID NO:

3.

10. The construction method according to claim 9, characterized in that, The positive strand of the siRNA includes SEQ ID NO: 4-6, more preferably SEQ ID NO: 6; and / or, The antisense strand of the siRNA includes SEQ ID NO: 7-9, more preferably SEQ ID NO: 9.