肾上腺素能、胆碱能和羟色胺能系统对子宫肌瘤发展和治疗的遗传贡献。

IF 1.5 Q3 MEDICINE, RESEARCH & EXPERIMENTAL International Journal of Molecular and Cellular Medicine Pub Date : 2023-01-01 DOI:10.22088/IJMCM.BUMS.12.4.320
Ângel Inácio, Laura Aguiar, Raquel Carrilho, Patrícia Pires, Joana Ferreira, Luís Coelho, Mário Rui Mascarenhas, Luís Sardinha, Tiago Bilhim, João Pisco, Manuel Bicho, Maria Clara Bicho
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引用次数: 0

摘要

自律神经系统与肿瘤生物学之间的联系正在展开。我们旨在研究肾上腺素能系统(ADBR2 - rs1042713, NM_000024.6:c.46G>A, NP_000015.2:p. Gly16Arg)、胆碱能系统(CHRNA5 - rs16969968, NM_000745.3:c.1192G>A,NP_000736.2:p.Asp398Asn)和血清素能系统(SLC6A4 - 5-HTTVNTR-intron2, HTR2A - rs6313, NM_000621.5:c.102C>T, NP_ 001365853 .1: p. Ser 34=)对妇科肿瘤发生和栓塞治疗的影响。共分析了 517 份女性 DNA 样本。通过 PCR、PCR-RFLP 和 EndPoint 基因分型对样本进行了基因分型。结果显示,ADBR2 基因的 AA 基因型和 CHRNA5 基因的 GG 基因型与子宫肌瘤有统计学意义(OR = 2.311; p = 0.003 和 OR = 2.165; p = 0.001),基因型之间的表观交互作用会增加风险(OR = 2.458; p= 0.043)。基因型为 GG(CHRNA5)的患者在接受治疗后,主要子宫肌瘤的体积缩小幅度较小(p=0.015)。12/12-AA(SLC6A4 - ADBR2)基因型组合会增加患子宫肌瘤的风险(OR = 2.540,p= 0.030)。HTR2A 基因的 TT 基因型与两种风险基因型(ADBR2 或 CHRNA5)中的任何一种结合,都会大幅增加患癌风险(OR=5.266,p=0.006;OR=6.364,p=0.007)。我们的结论是,ADBR2 和 CHRNA5 基因具有相关作用,而与 HTR2A 和 SLC6A4 基因的表观关系增强了这种作用。CHRNA5 基因也可能是栓塞成功与否的调节因子。我们证实了自主神经系统遗传学对肿瘤生物学的贡献。
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Genetic Contribution of the Adrenergic, Cholinergic, and Serotonergic Systems to Leiomyoma Development and Treatment.

The link between the autonomic nervous system and tumor biology is being unfold. We aim to study the contribution of genes of the adrenergic (ADBR2 - rs1042713, NM_000024.6:c.46G>A, NP_000015.2:p. Gly16Arg), cholinergic (CHRNA5 - rs16969968, NM_000745.3:c.1192G>A, NP_000736.2:p.Asp398Asn), and serotonergic systems (SLC6A4 - 5-HTTVNTR-intron2, HTR2A - rs6313, NM_000621.5:c.102C>T, NP_ 001365853 .1: p. Ser 34=) to gynecological tumorigenesis and their treatment by embolization. A total of 517 DNA samples from women were analyzed. Samples were genotyped by PCR, PCR-RFLP and EndPoint genotyping. Results show a statistically significant association between the AA genotype of the ADBR2 gene and GG genotype of the CHRNA5 gene with leiomyoma (OR = 2.311; p = 0.003 and OR = 2.165; p = 0.001, respectively), and the epistatic interaction between genotypes increases the risk (OR = 2.458; p= 0.043). The GG genotype (CHRNA5) shows a lower reduction of the volume of the main leiomyoma after treatment (p=0.015). Combination of the genotypes 12/12-AA (SLC6A4 - ADBR2) increases the risk to leiomyoma (OR = 2.540, p= 0.030). TT genotype of HTR2A gene in combination with any of the two risk genotypes (of ADBR2 or CHRNA5) increases substantially the risk (OR = 5.266, p = 0.006; OR = 6.364, p=0.007, respectively). We conclude that ADBR2 and CHRNA5 genes have a relevant role that is enhanced by the epistatic relationship with the genes HTR2A and SLC6A4. CHRNA5 gene may also be a modulator of the success of embolization. We confirm the contribution of the genetics of Autonomous Nervous System to tumor biology.

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期刊介绍: The International Journal of Molecular and Cellular Medicine (IJMCM) is a peer-reviewed, quarterly publication of Cellular and Molecular Biology Research Center (CMBRC), Babol University of Medical Sciences, Babol, Iran. The journal covers all cellular & molecular biology and medicine disciplines such as the genetic basis of disease, biomarker discovery in diagnosis and treatment, genomics and proteomics, bioinformatics, computer applications in human biology, stem cells and tissue engineering, medical biotechnology, nanomedicine, cellular processes related to growth, death and survival, clinical biochemistry, molecular & cellular immunology, molecular and cellular aspects of infectious disease and cancer research. IJMCM is a free access journal. All open access articles published in IJMCM are distributed under the terms of the Creative Commons Attribution CC BY. The journal doesn''t have any submission and article processing charges (APCs).
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