2021
DOI: 10.1016/j.jsbmb.2021.105844
|View full text |Cite
|
Sign up to set email alerts
|

miR-130b-3p is high-expressed in polycystic ovarian syndrome and promotes granulosa cell proliferation by targeting SMAD4

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
5
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 11 publications
(6 citation statements)
references
References 43 publications
0
5
0
Order By: Relevance
“…MicroRNAs (miRNAs) are ~22nt long small and non-coding RNAs that directly target the 3′-UTR region of mRNAs, thus affecting mRNA transcription and translation [ 5 , 6 ]. miRNAs have been reported to have essential functions in metabolic disorders, including PCOS [ 7 9 ].…”
Section: Introductionmentioning
confidence: 99%
“…MicroRNAs (miRNAs) are ~22nt long small and non-coding RNAs that directly target the 3′-UTR region of mRNAs, thus affecting mRNA transcription and translation [ 5 , 6 ]. miRNAs have been reported to have essential functions in metabolic disorders, including PCOS [ 7 9 ].…”
Section: Introductionmentioning
confidence: 99%
“…The reversal of hypoxia can cause the decrease of SIRT1 activity in mitochondria and during hypoxia. [48][49][50] The ovarian GC of PCOS patients show abnormal proliferation, which can be reversed by reducing cell proliferation and inhibiting apoptosis with inhibitors. [51] Nitric oxide (NO) plays a role in the physiology of the reproductive system, follicular development and selection, is associated with angiogenic events, play a regulatory role in steroid production in ovarian cells by stimulating cyclooxygenase-2 activity, NO induces increased production of prostaglandin E2, which appears to be a common ovulation mechanism, NO level is negatively correlated with IR in PCOS patients, and the effects of NO and IR are mutually reinforcing, many of the effects of insulin depend on NO, which is an effector in insulin information transduction pathway.…”
Section: Discussionmentioning
confidence: 99%
“…BMP4 treatment suppressed androgen synthesis in thecal cells and promoted estrogen production in granulosa cells by regulating the expression of steroidogenic enzymes, including CYP11A, HSD3B2, CYP17A1, and CYP19A1. BMP4 levels are significantly decreased in hyperandrogenism [ 218 , 219 ]. The role of miR-29a in the regulation of the inflammatory background via AR needs clarification.…”
Section: Epigenetic Modulation Of Androgenic Activity In Response To ...mentioning
confidence: 99%