Evidence map›Paper›PMID 35908193›Full record

ReviewMolecular reproduction and development2022

Regulation of oocyte maturation: Role of conserved ERK signaling.

Debabrata Das, Swathi Arur

Open access · greenAbstract readReview
In one paragraph

Review in Molecular reproduction and development, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. IGF-1 supplementation improvesFrontiers in veterinary science · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Expression ofInternational journal of reproductive biomedicine · 2025
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
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  17. Article
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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

2 authors at 1 institution in 1 country.

Debabrata DasDepartment of Genetics, UT MD Anderson Cancer Center, Houston, Texas, USA.
Swathi ArurDepartment of Genetics, UT MD Anderson Cancer Center, Houston, Texas, USA.ORCID 0000-0002-6941-2711
The University of Texas MD Anderson Cancer Center · US

Funding

How Post-Translational Codes and Small RNA Pathways Shape Developmental OutcomesR35GM140933 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Swathi Arur · 2021 to 2026
$2.5M
ERK mediated regulation of RbAp46/48 during female germ cell developmentR01HD101269 · NICHD · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ARUR, SWATHI · 2020 to 2024
$1.6M
NICHD NIH HHS R01 HD101269NIGMS NIH HHS R35 GM140933
6 · The paper itself

Abstract

During oogenesis, oocytes arrest at meiotic prophase I to acquire competencies for resuming meiosis, fertilization, and early embryonic development. Following this arrested period, oocytes resume meiosis in response to species-specific hormones, a process known as oocyte maturation, that precedes ovulation and fertilization. Involvement of endocrine and autocrine/paracrine factors and signaling events during maintenance of prophase I arrest, and resumption of meiosis is an area of active research. Studies in vertebrate and invertebrate model organisms have delineated the molecular determinants and signaling pathways that regulate oocyte maturation. Cell cycle regulators, such as cyclin-dependent kinase (CDK1), polo-like kinase (PLK1), Wee1/Myt1 kinase, and the phosphatase CDC25 play conserved roles during meiotic resumption. Extracellular signal-regulated kinase (ERK), on the other hand, while activated during oocyte maturation in all species, regulates both species-specific, as well as conserved events among different organisms. In this review, we synthesize the general signaling mechanisms and focus on conserved and distinct functions of ERK signaling pathway during oocyte maturation in mammals, non-mammalian vertebrates, and invertebrates such as Drosophila and Caenorhabditis elegans.

Indexed as

Drosophila ProteinsMeiosisAnimalsCaenorhabditis elegansCyclin-Dependent KinasesDrosophilaExtracellular Signal-Regulated MAP KinasesFemaleHormonesMammalsOocytesOogenesisPhosphoric Monoester HydrolasesProtein KinasesSignal TransductionCyclin-Dependent KinasesDrosophila ProteinsExtracellular Signal-Regulated MAP KinasesHormonesMyt1 protein, DrosophilaPhosphoric Monoester HydrolasesProtein Kinasescyclin B/CDK1ERKmeiosisoocyte maturationoogenesis

Identifiers

PMID35908193
PMCPMC9492652
OpenAlexW4288941083

What OpenQuestion holds

Textmetadata
LicenceTDM
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.