Emerging roles for the RXFP1 in myeloid series leukemia

Ayriana Safari Baesmat, Berna Bayrakdar
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Abstract

Purpose: The study investigates the role of Relaxin Family Peptide Receptor 1 (RXFP1) in myeloid leukemia cell function. It found that RXFP1 has been associated with cAMP, PI3K/Akt, NO/cGMP, MAPK and ERK1/2 signaling. High RXFP1 expression was associated with shorter cancer-specific survival RXFP1 mutated leukemia patients. The study suggests that RXFP1 may promote invasion and progression in both types of AML and CML. Methods: The gene expression data were retrieved from Gene Expression Omnibus (GEO). Fold change, p.value t-test and David Functional analysis, hierarchical clustering was performed. Conclusion: PCDH9, AREG, CTSG, RXFP1, CCDC152, ANXA, CD24 and VPREB1 gene expression alterations were identified depending on leukemia in human moocyte cells. Seven of these genes were identified as downregulated in leukemia groups in human monocyte cells and one of these genes were identified as upregulated in leukemia cells.Therefore, it is hypothesized that downregulation or upregulation of these genes may affect AML/CML pathogenesis by reducing cell proliferation. And it is predicted that RXFP1 mutation may be an important factor for myeloid leukemia.
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RXFP1 在骨髓系列白血病中的新作用
目的:本研究探讨了松弛素家族肽受体 1(RXFP1)在骨髓性白血病细胞功能中的作用。研究发现,RXFP1 与 cAMP、PI3K/Akt、NO/cGMP、MAPK 和 ERK1/2 信号传导有关。RXFP1的高表达与RXFP1突变的白血病患者较短的癌症特异性生存期有关。该研究表明,RXFP1 可能会促进急性髓细胞性白血病和慢性骨髓性白血病两种类型的侵袭和进展。研究方法基因表达数据取自基因表达总库(GEO)。进行折线变化、p.value t 检验和大卫功能分析、层次聚类。结论根据人嗜酸性粒细胞白血病的情况,确定了 PCDH9、AREG、CTSG、RXFP1、CCDC152、ANXA、CD24 和 VPREB1 基因表达的改变。因此,假设这些基因的下调或上调可能会通过减少细胞增殖而影响 AML/CML 的发病机制。预计 RXFP1 基因突变可能是导致髓性白血病的一个重要因素。
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