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Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
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Application of Laser Microdissection to Uncover Regional Transcriptomics in Human Kidney Tissue
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Decoding Kidney Pathophysiology: Omics-Driven Approaches in Precision Medicine.

Charlotte Delrue1, Marijn M Speeckaert1,2

  • 1Department of Nephrology, Ghent University Hospital, 9000 Ghent, Belgium.

Journal of Personalized Medicine
|December 27, 2024
PubMed
Summary
This summary is machine-generated.

Precision medicine uses multi-omics to understand chronic kidney disease (CKD) heterogeneity. This approach aims to improve diagnosis, identify biomarkers, and personalize treatments for better patient outcomes.

Keywords:
kidney disease biomarkersmulti-omicsprecision medicine

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Area of Science:

  • Nephrology
  • Genomics
  • Proteomics
  • Metabolomics
  • Epigenomics

Background:

  • Chronic kidney disease (CKD) is a global health issue with complex biology and progressive nature.
  • Current diagnostic and therapeutic methods often lack efficacy due to disease heterogeneity.
  • Precision medicine offers a personalized approach to kidney disease research and treatment.

Purpose of the Study:

  • To explore the role of precision medicine in understanding and treating chronic kidney disease.
  • To highlight the application of multi-omics technologies in identifying CKD subtypes and therapeutic targets.
  • To discuss the potential of personalized treatment strategies for improving patient outcomes.

Main Methods:

  • Integration of multi-omics data, including genomics, transcriptomics, proteomics, metabolomics, and epigenomics.
  • Application of pharmacogenomics for predicting treatment responses.
  • Utilizing single-cell and spatial transcriptomics to analyze biological heterogeneity.

Main Results:

  • Multi-omics integration enhances understanding of CKD by revealing molecular pathways involved in progression and treatment resistance.
  • Identification of discrete disease subtypes, molecular biomarkers, and potential therapeutic targets.
  • Insights into biological heterogeneity and personalized treatment responses.

Conclusions:

  • Precision medicine, through multi-omics, offers a promising avenue for advancing CKD diagnosis, risk assessment, and personalized care.
  • Overcoming challenges like data integration, cost, and ethical considerations is crucial for realizing its full potential.
  • Development of standardized protocols, data-sharing frameworks, and advanced computational tools will drive innovation in nephrology.