Abstract
HELLP syndrome is a disorder during pregnancy which is defined by elevation of liver enzymes, haemolysis, and low platelet count. This syndrome is a multifactorial one and both genetic and environmental components can have a crucial role in this syndrome’s pathogenesis. Long noncoding RNAs (lncRNAs), are defined as long non-protein coding molecules (more than 200 nucleotides), which are functional units in most cellular processes such as cell cycle, differentiation, metabolism and some diseases progression. As these markers discovered, there has been some evidence that they have an important role in the function of some organs, such as placenta; therefore, alteration and dysregulation of these RNAs can develop or alleviate HELLP disorder. Although the role of lncRNAs has been shown in HELLP syndrome, the process is still unclear. In this review, our purpose is to evaluate the association between molecular mechanisms of lncRNAs and HELLP syndrome pathogenicity to elicit some novel approaches for HELLP diagnosis and treatment.
Acknowledgements
The authors thank you of all our colleague in IRAN university of medical science.
Ethical approval
This article does not contain any studies with human participants or animals performed by any of the authors.
Author contributions
Sh,A and BZ has conceived the manuscript and revised it. Z,K, K,S and M,F,Z wrote the manuscript. E,Gh and S,A design the table and edited language.
Disclosure statement
No potential conflict of interest was reported by the author(s).
Data availability statement
This is a review study, and it is not an original. Data availability is corresponding author responsibility.