Literature DB >> 31280217

Association Between hsa-miR-30e Polymorphisms and Sporadic Primary Hyperparathyroidism Risk.

Maria Mizamtsidi1, Konstantinos Nastos2, Fausto Palazzo3, Vasilis Constantinides3, Roberto Dina4, Megan Farenden5, George Mastorakos6, Ioannis Vassiliou2, Maria Gazouli5.   

Abstract

BACKGROUND/AIM: Almost 15% of patients with sporadic primary hyperparathyroidism (sPHPT) present with multiple gland disease (MGD). The aim of this study was to investigate the potential role of two polymorphisms of the hsa-miR-30e, in sPHPT tumorigenesis. PATIENTS AND METHODS: One-hundred twenty sPHPT patients, 77 presenting a single adenoma and 43 with MGD, and 54 healthy controls were genotyped. The SNPs were identified using the allele-specific PCR methodology, while the hsa-miR-30e expression was analyzed by real-time quantitative reverse transcriptase PCR.
RESULTS: Hsa-miR-30e expression was found to be significantly higher in patients with MGD compared to patients with single adenomas (p=0.0019), but no differences were found regarding specific genotype carriers. The genotype frequencies for ss178077483 and rs7556088 were significantly different between patients and healthy controls.
CONCLUSION: Although the polymorphisms cannot be used as biomarkers for the differential diagnosis of MGD, hsa-miR-30e expression could potentially serve as a biomarker for this purpose. Copyright
© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Entities:  

Keywords:  Sporadic primary hyperparathyroidism; adenoma; microRNA; multiple gland disease

Mesh:

Substances:

Year:  2019        PMID: 31280217      PMCID: PMC6689336          DOI: 10.21873/invivo.11598

Source DB:  PubMed          Journal:  In Vivo        ISSN: 0258-851X            Impact factor:   2.155


  30 in total

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2.  Differential RNA expression profile by cDNA microarray in sporadic primary hyperparathyroidism (pHPT): primary parathyroid hyperplasia versus adenoma.

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3.  Expression of nm23 antimetastatic gene product in parathyroid hyperplasia, adenoma and carcinoma. An immunohistological assessment.

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4.  Absence of somatic RET gene mutation in sporadic parathyroid tumors and hyperplasia secondary to uremia, and absence of somatic Men1 gene mutation in MEN2A-associated hyperplasia.

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5.  Parathyroid hyperplasia, adenomas, and carcinomas: differential expression of p27Kip1 protein.

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8.  Differential expression of microRNAs in human parathyroid carcinomas compared with normal parathyroid tissue.

Authors:  S Corbetta; V Vaira; V Guarnieri; A Scillitani; C Eller-Vainicher; S Ferrero; L Vicentini; I Chiodini; M Bisceglia; P Beck-Peccoz; S Bosari; A Spada
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9.  Chromosome 11 genomic changes in parathyroid adenoma and hyperplasia: array CGH, FISH, and tissue microarrays.

Authors:  Y Yi; Norma J Nowak; Annmarie L Pacchia; Carl Morrison
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10.  The profile of ErbB/Her family genes copy number assessed by real-time PCR in parathyroid adenoma and hyperplasia associated with sporadic primary hyperparathyroidism.

Authors:  Natalia Bednarz; Krzysztof Błaut; Krzysztof Sworczak; Tomasz Oseka; Krzysztof P Bielawski
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  1 in total

Review 1.  Molecular Mechanisms of Parathyroid Disorders in Chronic Kidney Disease.

Authors:  Alia Hassan; Nareman Khalaily; Rachel Kilav-Levin; Morris Nechama; Oded Volovelsky; Justin Silver; Tally Naveh-Many
Journal:  Metabolites       Date:  2022-01-25
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