CCL2 rs1024611Gene Polymorphism in Philadelphia-Negative Myeloproliferative Neoplasms

• Published in: Genes Vol. 13; no. 3; p. 492
• Main Authors: Hodeib, Hossam, Abd El Hai, Dina, Tawfik, Mohamed A, Allam, Alzahraa A, Selim, Amal, Elsawy, Abdallah Ahmed, Youssef, Amira
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 10.03.2022; MDPI
• Subjects: Blood; Cancer; Chemokine CCL2 - genetics; Cloning; Cytokines; Fibrosis; Gene expression; Gene polymorphism; Genes; Genetic testing; Genotype; Humans; Lymphoma; Monocyte chemoattractant protein 1; Mutation; Myeloproliferative Disorders - genetics; Pathogenesis; Philadelphia chromosome; Polycythemia Vera - genetics; Polymerase chain reaction; Polymorphism; Polymorphism, Genetic; Primary Myelofibrosis - genetics; Risk factors; Single-nucleotide polymorphism; Solid tumors; Tumors; United States > US; Germany; Egypt; polymorphism; CCL2 rs1024611Gene; Philadelphia; myeloproliferative
• ISSN: 2073-4425; 2073-4425
• DOI: 10.3390/genes13030492

Introduction: The onset of the Philadelphia chromosome-negative myeloproliferative neoplasms (MPNs) is caused by acquired somatic mutations in target myeloid genes “driver mutations”. The CCL2 gene is overexpressed by non-Hodgkin lymphomas and multiple solid tumors. Aim of the study: to evaluate the possible association of CCL2 rs1024611 SNP and its expression level and the risk of developing Philadelphia-negative MPNs. Patients and methods: A total of 128 newly diagnosed Philadelphia-negative MPN patient and 141 healthy subjects were evaluated for the genotype distribution of CCL2 rs1024611 and CCL2 expression levels. Results: The CCL2 rs1024611 G/G genotype was more frequent and significantly frequent among PMF and Post-PV/ET-MF patients and the mean CCL2 expression levels were significantly higher in PMF and Post-PV/ET-MF compared to the healthy subjects. The CCL2 rs1024611 SNP was significantly correlated to the CCL2 gene expression level and fibrosis grade. ROC analysis for the CCL2 gene expression level that discriminates MF patients from PV + ET patients revealed a sensitivity of 80.43% and a specificity of 73.17% with an AUC of 0.919 (p < 0.001). Conclusion: The CCL2 rs1024611 polymorphism could be an independent risk factor for developing MF (PMF and Post-PV/ET-MF). Moreover, CCL2 gene expression could be potential genetic biomarker of fibrotic progression.