Skip to main content
Have a personal or library account? Click to login
Expression Analysis of Adrenomedullin and Its Receptors RAMP2/CLR and RAMP3/CLR in Acute Myeloid Leukemia: A Saudi Cohort Study Cover

Expression Analysis of Adrenomedullin and Its Receptors RAMP2/CLR and RAMP3/CLR in Acute Myeloid Leukemia: A Saudi Cohort Study

Open Access
|Apr 2026

Abstract

Acute myeloid leukemia (AML) is a complex and aggressive malignancy, particularly in children, characterized by chromosomal abnormalities and diverse gene mutations, which contribute to its variable clinical outcomes. Despite advancements in treatment, the prognosis for AML patients remains poor, highlighting the urgent need for reliable biomarkers. Adrenomedullin (ADM), a peptide expressed in various cancer cells, has been implicated in tumor progression. In this study, we investigated the expression patterns and quantified the levels of ADM and its associated receptors receptor activity-modifying proteins (RAMP)2, RAMP3, and calcitonin receptor-like receptor (CLR) in Saudi AML patients. Using real-time PCR and protein analysis, we compared the gene and protein expression levels of these molecules in serum samples from AML patients and healthy controls. Our findings revealed a significant increase (p = 0.0001) in the gene expression of ADM, RAMP2, RAMP3, and CLR in AML patients compared to healthy controls. Furthermore, protein levels of ADM and RAMP3 were significantly elevated (p = 0.0001) in the patient group. These findings suggest that ADM and its receptor components may serve as promising diagnostic biomarkers and potential therapeutic targets for acute myeloid leukemia, warranting further clinical validation.

Language: English
Page range: 46 - 54
Published on: Apr 30, 2026
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2026 Sadeem Aljabr, Ramesa Shafi Bhat, Nada Al Qahtani, Emad Kutbi, Mona Alonazi, Shahad AlOtaiby, Sooad Al-Daihan, published by European Biotechnology Thematic Network Association
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.