» Articles » PMID: 36761351

Competing Endogenous RNA (ceRNA) Networks in Parkinson's Disease: A Systematic Review

Abstract

Parkinson's disease (PD) is a distinctive clinical syndrome with several causes and clinical manifestations. Aside from an infectious cause, PD is a rapidly developing neurological disorder with a global rise in frequency. Notably, improved knowledge of molecular pathways and the developing novel diagnostic methods may result in better therapy for PD patients. In this regard, the amount of research on ceRNA axes is rising, highlighting the importance of these axes in PD. CeRNAs are transcripts that cross-regulate one another competition for shared microRNAs (miRNAs). These transcripts may be either coding RNAs (mRNAs) or non-coding RNAs (ncRNAs). This research used a systematic review to assess validated loops of ceRNA in PD. The Prisma guideline was used to conduct this systematic review, which entailed systematically examining the articles of seven databases. Out of 309 entries, forty articles met all criteria for inclusion and were summarized in the appropriate table. CeRNA axes have been described through one of the shared vital components of the axes, including lncRNAs such as NEAT1, SNHG family, HOTAIR, MALAT1, XIST, circRNAs, and lincRNAs. Understanding the multiple aspects of this regulatory structure may aid in elucidating the unknown causal causes of PD and providing innovative molecular therapeutic targets and medical fields.

Citing Articles

Bibliometric analysis of microRNAs and Parkinson's disease from 2014 to 2023.

Chen L, Chen J, Weng W, Wu M, Zhou X, Yan P Front Neurol. 2024; 15:1466186.

PMID: 39385824 PMC: 11462628. DOI: 10.3389/fneur.2024.1466186.


Exploring the Regulatory Landscape of Dementia: Insights from Non-Coding RNAs.

Kim J, Kim W, Park E, Lee D, Lee Y, Shin H Int J Mol Sci. 2024; 25(11).

PMID: 38892378 PMC: 11172830. DOI: 10.3390/ijms25116190.


Integrative analysis of plasma and substantia nigra in Parkinson's disease: unraveling biomarkers and insights from the lncRNA-miRNA-mRNA ceRNA network.

Chun K, Kim S Front Aging Neurosci. 2024; 16:1388655.

PMID: 38784444 PMC: 11112011. DOI: 10.3389/fnagi.2024.1388655.


Integrated bioinformatics analysis for exploring potential biomarkers related to Parkinson's disease progression.

Huang Z, Song E, Chen Z, Yu P, Chen W, Lin H BMC Med Genomics. 2024; 17(1):133.

PMID: 38760670 PMC: 11100188. DOI: 10.1186/s12920-024-01885-9.


The multifaceted functions of long non-coding RNA in neuropathologies and its potential as a prognostic marker and therapeutic biotarget.

Ahmad F, Sudesh R, Ahmed A, Arumugam M, Mathkor D, Haque S Expert Rev Mol Med. 2024; 26:e11.

PMID: 38682637 PMC: 11140545. DOI: 10.1017/erm.2024.11.


References
1.
Hu X, Yang L, Mo Y . Role of Pseudogenes in Tumorigenesis. Cancers (Basel). 2018; 10(8). PMC: 6115995. DOI: 10.3390/cancers10080256. View

2.
Nawa M, Matsuoka M . KCTD20, a relative of BTBD10, is a positive regulator of Akt. BMC Biochem. 2013; 14:27. PMC: 3827329. DOI: 10.1186/1471-2091-14-27. View

3.
Sanders L, McCoy J, Hu X, Mastroberardino P, Dickinson B, Chang C . Mitochondrial DNA damage: molecular marker of vulnerable nigral neurons in Parkinson's disease. Neurobiol Dis. 2014; 70:214-23. PMC: 4144978. DOI: 10.1016/j.nbd.2014.06.014. View

4.
Wang K, Chang H . Molecular mechanisms of long noncoding RNAs. Mol Cell. 2011; 43(6):904-14. PMC: 3199020. DOI: 10.1016/j.molcel.2011.08.018. View

5.
Zhang L, Wang J, Liu Q, Xiao Z, Dai Q . Knockdown of long non-coding RNA AL049437 mitigates MPP+ -induced neuronal injury in SH-SY5Y cells via the microRNA-205-5p/MAPK1 axis. Neurotoxicology. 2020; 78:29-35. DOI: 10.1016/j.neuro.2020.02.004. View