Evidence map›Paper›PMID 34975760›Full record

ReviewFrontiers in endocrinology2021

Ovarian Aging: Role of Pituitary-Ovarian Axis Hormones and ncRNAs in Regulating Ovarian Mitochondrial Activity.

Marco Colella, Danila Cuomo, Teresa Peluso, Ilaria Falanga, Massimo Mallardo, Mario De Felice, Concetta Ambrosino

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.8field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Article
  3. Anti-Müllerian hormone and somatic ovarian function: a new perspective.Journal of assisted reproduction and genetics · 2026
    Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
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  13. Animals : an open access journal from MDPI · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Exploring the protective effects of coenzyme Q10 on female fertility.Frontiers in cell and developmental biology · 2025
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 2 countries.

Marco ColellaBiogem, Istituto di Biologia e Genetica Molecolare, Ariano Irpino, Italy.
Danila CuomoDepartment of Molecular and Cellular Medicine, College of Medicine, Texas A&M University, College Station, TX, United States.
Teresa PelusoDepartment of Science and Technology, University of Sannio, Benevento, Italy.
Ilaria FalangaDepartment of Science and Technology, University of Sannio, Benevento, Italy.
Massimo MallardoDepartment of Molecular Medicine and Medical Biotechnologies, University of Naples "Federico II", Naples, Italy.
Mario De FeliceDepartment of Molecular Medicine and Medical Biotechnologies, University of Naples "Federico II", Naples, Italy.
Concetta AmbrosinoBiogem, Istituto di Biologia e Genetica Molecolare, Ariano Irpino, Italy.
University of Naples Federico II · ITUniversity of Sannio · ITBiogem · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITTexas A&M University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The number of mitochondria in the oocyte along with their functions (e.g., energy production, scavenger activity) decline with age progression. Such multifaceted functions support several processes during oocyte maturation, ranging from energy supply to synthesis of the steroid hormones. Hence, it is hardly surprising that their impairment has been reported in both physiological and premature ovarian aging, wherein they are crucial players in the apoptotic processes that arise in aged ovaries. In any form, ovarian aging implies the progressive damage of the mitochondrial structure and activities as regards to ovarian germ and somatic cells. The imbalance in the circulating hormones and peptides (e.g., gonadotropins, estrogens, AMH, activins, and inhibins), active along the pituitary-ovarian axis, represents the biochemical sign of ovarian aging. Despite the progress accomplished in determining the key role of the mitochondria in preserving ovarian follicular number and health, their modulation by the hormonal signalling pathways involved in ovarian aging has been poorly and randomly explored. Yet characterizing this mechanism is pivotal to molecularly define the implication of mitochondrial dysfunction in physiological and premature ovarian aging, respectively. However, it is fairly difficult considering that the pathways associated with ovarian aging might affect mitochondria directly or by altering the activity, stability and localization of proteins controlling mitochondrial dynamics and functions, either unbalancing other cellular mediators, released by the mitochondria, such as non-coding RNAs (ncRNAs). We will focus on the mitochondrial ncRNAs (i.e., mitomiRs and mtlncRNAs), that retranslocate from the mitochondria to the nucleus, as active players in aging and describe their role in the nuclear-mitochondrial crosstalk and its modulation by the pituitary-ovarian hormone dependent pathways. In this review, we will illustrate mitochondria as targets of the signaling pathways dependent on hormones and peptides active along the pituitary/ovarian axis and as transducers, with a particular focus on the molecules retrieved in the mitochondria, mainly ncRNAs. Given their regulatory function in cellular activities we propose them as potential diagnostic markers and/or therapeutic targets.

Indexed as

AgingAndrogensAnimalsCell NucleusDNA, MitochondrialEstrogensFemaleFollicular AtresiaGonadotropins, PituitaryHumansMitochondriaMutationOvaryRNA, UntranslatedSignal TransductionAndrogensDNA, MitochondrialEstrogensGonadotropins, PituitaryRNA, UntranslatedestrogensFSH (follicle stimulating hormone)LncRNA - long noncoding RNAmiRNA - microRNAmitochondriaMitomiRsncRNAovarian aging

Identifiers

PMID34975760
PMCPMC8716494
OpenAlexW4200614630

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.