Evidence map›Paper›PMID 30665407›Full record

ReviewJournal of biomedical science2019

Necroptosis in stressed ovary.

Govind R Chaudhary, Pramod K Yadav, Anil K Yadav, Meenakshi Tiwari, Anumegha Gupta, Alka Sharma, Ashutosh N Pandey, Ajai K Pandey, Shail K Chaube

Open access · diamondAbstract readReview
In one paragraph

Review in Journal of biomedical science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Relationship between different modes of death and premature ovarian insufficiency: a literature review.Apoptosis : an international journal on programmed cell death · 2026
    Review
  6. Article
  7. Review
  8. Lemongrass (Biochemistry research international · 2026
    Article
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  14. Review
  15. 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

9 authors at 1 institution in 1 country.

Govind R ChaudharyCell Physiology Laboratory, Department of Zoology, Institute of Science, Banaras Hindu University, 221005, Varanasi, India.
Pramod K YadavCell Physiology Laboratory, Department of Zoology, Institute of Science, Banaras Hindu University, 221005, Varanasi, India.
Anil K YadavCell Physiology Laboratory, Department of Zoology, Institute of Science, Banaras Hindu University, 221005, Varanasi, India.
Meenakshi TiwariCell Physiology Laboratory, Department of Zoology, Institute of Science, Banaras Hindu University, 221005, Varanasi, India.
Anumegha GuptaCell Physiology Laboratory, Department of Zoology, Institute of Science, Banaras Hindu University, 221005, Varanasi, India.
Alka SharmaCell Physiology Laboratory, Department of Zoology, Institute of Science, Banaras Hindu University, 221005, Varanasi, India.
Ashutosh N PandeyCell Physiology Laboratory, Department of Zoology, Institute of Science, Banaras Hindu University, 221005, Varanasi, India.
Ajai K PandeyDepartment of Kayachikitsa, Faculty of Ayurveda, Institute of Medical Science, Banaras Hindu University, 221005, Varanasi, India.
Shail K ChaubeCell Physiology Laboratory, Department of Zoology, Institute of Science, Banaras Hindu University, 221005, Varanasi, India. shailchaubey@gmail.com.ORCID http://orcid.org/0000-0003-0230-3462
Banaras Hindu University · IN

Funding

Department of Science and Technology, Ministry of Science and Technology, Government of India EMR/2014/000702
6 · The paper itself

Abstract

Stress is deeply rooted in the modern society due to limited resources and large competition to achieve the desired goal. Women are more frequently exposed to several stressors during their reproductive age that trigger generation of reactive oxygen species (ROS). Accumulation of ROS in the body causes oxidative stress (OS) and adversely affects ovarian functions. The increased OS triggers various cell death pathways in the ovary. Beside apoptosis and autophagy, OS trigger necroptosis in granulosa cell as well as in follicular oocyte. The OS could activate receptor interacting protein kinase-1(RIPK1), receptor interacting protein kinase-3 (RIPK3) and mixed lineage kinase domain-like protein (MLKL) to trigger necroptosis in mammalian ovary. The granulosa cell necroptosis may deprive follicular oocyte from nutrients, growth factors and survival factors. Under these conditions, oocyte becomes more susceptible towards OS-mediated necroptosis in the follicular oocytes. Induction of necroptosis in encircling granulosa cell and oocyte may lead to follicular atresia. Indeed, follicular atresia is one of the major events responsible for the elimination of majority of germ cells from cohort of ovary. Thus, the inhibition of necroptosis could prevent precautious germ cell depletion from ovary that may cause reproductive senescence and early menopause in several mammalian species including human.

Indexed as

Stress, PhysiologicalAnimalsApoptosisFemaleHumansNecrosisOvaryOxidative StressReactive Oxygen SpeciesReactive Oxygen SpeciesMLKLNecroptosisOvaryOxidative stressRIPKStressTNF

Identifiers

PMID30665407
PMCPMC6340166
OpenAlexW2920663807

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.