Journals / İstanbul Kuzey Klinikleri / 2018 / Cilt: 5 - Sayı: 3

Ear atresia: Is there a role of apoptosis-regulating miRNAs?

Pages
238–245
Publication Date
2022-10-18
DOI
—
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

This isthe first report to present the possible association between apoptosis-regulating miRNAs and ear atresia/microtia.

📌 3 Key Takeaways

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Objective & Hypothesis:OBJECTIVE: The molecular events underlying ear development involve numerous regulatory molecules; however, the roleof microRNAs (miRNAs) has not been explored in patients with ear atresia.
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Key Findings & Data:Here, we aimed to investigate the expressions of20–22 nucleotide noncoding RNAs.METHODS: We selected 12 miRNAs that function to control post-transcriptional gene expression in different pathways, including apoptosis, angiogenesis, and chondrogenesis.
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Conclusion & Impact:This isthe first report to present the possible association between apoptosis-regulating miRNAs and ear atresia/microtia.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

OBJECTIVE: The molecular events underlying ear development involve numerous regulatory molecules; however, the roleof microRNAs (miRNAs) has not been explored in patients with ear atresia. Here, we aimed to investigate the expressions of20–22 nucleotide noncoding RNAs.METHODS: We selected 12 miRNAs that function to control post-transcriptional gene expression in different pathways, including apoptosis, angiogenesis, and chondrogenesis. The altered miRNA expressions were analyzed by real-time PCR fromserum samples of 7 patients with ear atresia and 8 controls.RESULTS: We found that the expression of apoptosis-regulating miRNAs was significantly downregulated in patients with earatresia. TThe expressions of miR126, miR146a, miR222, and miR21 were significantly decreased by 76.2-(p=0.041), 61.8-(p=0.000), 30.5-(p=0.009), and 71.21-fold (p=0.042), respectively, compared with controls.CONCLUSION: Abnormal ear development in ear atresia patients, could possibly be due to the reduced expression of apoptosis regulating miRNAs. Changes in the regulation of tumor protein p53 (TP53), p53 upregulated modulator of apoptosis(PUMA), Fas cell surface death receptor (FAS), FAS ligand (FasL), and phosphatase and tensin homolog (PTEN) directly orwithin the apoptosis-related cascades may play important roles during development, particularly in the external ear. This isthe first report to present the possible association between apoptosis-regulating miRNAs and ear atresia/microtia.

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Cite This Article

AKBAŞ, E., ASLAN, E., YILDIRIM, S., AKALIN, İ., YILMAZ, S., YILMAZ, S., KARAOĞLU, A. S., TELLİ, U., GÜDEK, H., KALCIOĞLU, M. T. (2022). Ear atresia: Is there a role of apoptosis-regulating miRNAs?. İstanbul Kuzey Klinikleri, Cilt: 5 - Sayı: 3, 238–245. https://ajindex.com/articles/551545

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References (18)

  1. Nager GT. Congenital aural atresia: anatomy and surgical management. Birth Defects Orig Artic Ser 1971;07:33–51
  2. Castilla EE, Orioli IM. Prevalence rates of microtia in South America. Int J Epidemiol 1986;15:364–8
  3. Dostal A, Nemeckova J, Gaillyova R, Vranova V, Zezulkova D, Lejska M, et al. Identification of 2.3-Mb gene locus for congenital aural atresia in 18q22.3 deletion: a case report analyzed by comparative genomic hybridization. Otol Neurotol 2006;27:427–32
  4. Jones KL, Jones MC, Del Campo M. Smith’s reconnisable patterns of human malformations. 7th ed. Philadelphia: Elsevier Saunders; 2013
  5. Wright CG. Development of the human external ear. J Am Acad Audiol 1997;8:379–82
  6. Peck JE. Development of hearing. Part II. Embryology. J Am Acad Audiol 1994;5:359–65
  7. Kenna MA. Embryology and developmental anatomy of the ear. In: Bluestone CD, Stool SE, editors. 2nd ed. Philadelphia: WB Saunders; 1990. p. 77–87
  8. Nishizaki K, Anniko M, Orita Y, Masuda Y, Yoshino T, Kanda S, et al. Programmed cell death in the development of the mouse external auditory canal. Anat Rec 1998;252:378–82
  9. Gerschenson LE, Rotello RJ. Apoptosis: a different type of cell death. FASEB J 1992;6:2450–5
  10. Wyllie AH. Apoptosis (the 1992 Frank Rose Memorial Lecture). Br J Cancer 1993;67:205–8
  11. Bartel DP. MicroRNAs: genomics, biogenesis, mechanism, and function. Cell 2004;116:281–97
  12. Krol J, Loedige I, Filipowicz W. The widespread regulation of microRNA biogenesis, function and decay. Nat Rev Genet 2010;11:597–610
  13. Huang Y, Shen XJ, Zou Q, Wang SP, Tang SM, Zhang GZ. Biological functions of microRNAs: a review. J Physiol Biochem 2011;67:129–39
  14. Su Z, Yang Z, Xu Y, Chen Y, Yu Q. MicroRNAs in apoptosis, autophagy and necroptosis. Oncotarget 2015;6:8474–90
  15. Rudnicki A, Isakov O, Ushakov K, Shivatzki S, Weiss I, Friedman LM, et al. Next-generation sequencing of small RNAs from inner ear sensory epithelium identifies microRNAs and defines regulatory pathways. BMC Genomics 2014;15:484
  16. Kersigo J, D’Angelo A, Gray BD, Soukup GA, Fritzsch B. The role of sensory organs and the forebrain for the development of the craniofacial shape as revealed by Foxg1-cre-mediated microRNA loss. Genesis 2011;49:326–41
  17. Li H, Kloosterman W, Fekete DM. MicroRNA-183 family members regulate sensorineural fates in the inner ear. J Neurosci 2010;30:3254– 63
  18. Soukup GA, Fritzsch B, Pierce ML, Weston MD, Jahan I, McManus MT, et al. Residual microRNA expression dictate