Exploring G Protein-Coupled Receptors in Hematological Cancers

Choi Har Tsang,  and , Pawel Kozielewicz*, 
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Abstract

Hematological cancers, such as lymphomas and leukemias, pose significant challenges in oncology, necessitating a deeper understanding of their molecular landscape to enhance therapeutic strategies. This article critically examines and discusses recent research on the roles of G protein-coupled receptors (GPCRs) in myeloma, lymphomas, and leukemias with a particular focus on pediatric acute lymphoblastic (lymphocytic) leukemia (ALL). By utilizing RNA sequencing (RNA-seq), we analyzed GPCR expression patterns in pediatric ALL samples (aged 3–12 years old), with a further focus on Class A orphan GPCRs. Our analysis revealed distinct GPCR expression profiles in pediatric ALL, identifying several candidates with aberrant upregulated expression compared with healthy counterparts. Among these GPCRs, GPR85, GPR65, and GPR183 have varying numbers of studies in the field of hematological cancers and pediatric ALL. Furthermore, we explored missense mutations of pediatric ALL in relation to the RNA gene expression findings, providing insights into the genetic underpinnings of this disease. By integrating both RNA-seq and missense mutation data, this article aims to provide an insightful and broader perspective on the potential correlations between specific GPCR and their roles in pediatric ALL.

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探索血液肿瘤中的 G 蛋白偶联受体
血液学癌症,如淋巴瘤和白血病,对肿瘤学提出了重大挑战,需要更深入地了解其分子景观以增强治疗策略。本文对G蛋白偶联受体(gpcr)在骨髓瘤、淋巴瘤和白血病中的作用的最新研究进行了批判性的检查和讨论,并特别关注儿童急性淋巴细胞白血病(ALL)。通过RNA测序(RNA-seq),我们分析了儿童ALL样本(3-12岁)中GPCR的表达模式,并进一步关注了a类孤儿GPCR。我们的分析揭示了儿童ALL中不同的GPCR表达谱,确定了几种与健康对照相比表达异常上调的候选基因。在这些gpcr中,GPR85、GPR65和GPR183在血液学癌症和儿科ALL领域有不同数量的研究。此外,我们探讨了小儿ALL的错义突变与RNA基因表达的关系,为这种疾病的遗传基础提供了见解。通过整合RNA-seq和错义突变数据,本文旨在为特异性GPCR及其在儿童ALL中的作用之间的潜在相关性提供一个有见地和更广泛的视角。
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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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