Evidence map›Paper›PMID 37511039›Full record

ArticleInternational journal of molecular sciences2023

Cyclophilin A as a Pro-Inflammatory Factor Exhibits Embryotoxic and Teratogenic Effects during Fetal Organogenesis.

Anastasiia Kalinina, Maria Semenova, Alexandra Bruter, Ekaterina Varlamova, Marina Kubekina, Natalia Pavlenko, Yulia Silaeva, Alexey Deikin, Elena Antoshina, Tatyana Gorkova and 6 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

16 authors at 5 institutions in 1 country.

Anastasiia KalininaN.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, 24 Kashirskoe Shosse, Moscow 115478, Russia.ORCID 0000-0002-6912-5579
Maria SemenovaDepartment of Embryology, Faculty of Biology, Moscow State University, 1/12 Leninskie Gory, Moscow 119992, Russia.
Alexandra BruterN.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, 24 Kashirskoe Shosse, Moscow 115478, Russia.
Ekaterina VarlamovaCenter for Precision Genome Editing and Genetic Technologies for Biomedicine, Institute of Gene Biology, Russian Academy of Sciences, 34/5 Vavilov Street, Moscow 119334, Russia.ORCID 0000-0002-8451-1216
Marina KubekinaCenter for Precision Genome Editing and Genetic Technologies for Biomedicine, Institute of Gene Biology, Russian Academy of Sciences, 34/5 Vavilov Street, Moscow 119334, Russia.
Natalia PavlenkoCenter for Precision Genome Editing and Genetic Technologies for Biomedicine, Institute of Gene Biology, Russian Academy of Sciences, 34/5 Vavilov Street, Moscow 119334, Russia.
Yulia SilaevaCore Facility Center, Institute of Gene Biology, Russian Academy of Sciences, 34/5 Vavilova Street, Moscow 119334, Russia.
Alexey DeikinUnited Center for Genetic Technologies, Belgorod State National Research University, 85 Pobedi Street, Belgorod 308001, Russia.ORCID 0000-0001-9960-0863
Elena AntoshinaN.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, 24 Kashirskoe Shosse, Moscow 115478, Russia.
Tatyana GorkovaN.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, 24 Kashirskoe Shosse, Moscow 115478, Russia.
Lubov TrukhanovaN.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, 24 Kashirskoe Shosse, Moscow 115478, Russia.
Alla SalminaResearch Center of Neurology, 80 Volokolamskoye Shosse, Moscow 125367, Russia.
Svetlana NovikovaResearch Center of Neurology, 80 Volokolamskoye Shosse, Moscow 125367, Russia.
Dmitry VoronkovResearch Center of Neurology, 80 Volokolamskoye Shosse, Moscow 125367, Russia.ORCID 0000-0001-5222-5322
Dmitry KazanskyN.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, 24 Kashirskoe Shosse, Moscow 115478, Russia.
Ludmila KhromykhN.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, 24 Kashirskoe Shosse, Moscow 115478, Russia.
Ministry of Health of the Russian Federation · RUInstitute of Gene Biology · RUResearch Center of Neurology · RUBelgorod National Research University · RULomonosov Moscow State University · RU

Funding

Russian Science Foundation 22-75-00004
6 · The paper itself

Abstract

The precise balance of Th1, Th2, and Th17 cytokines is a key factor in successful pregnancy and normal embryonic development. However, to date, not all humoral factors that regulate and influence physiological pregnancy have been completely studied. Our data here pointed out cyclophilin A (CypA) as the adverse pro-inflammatory factor negatively affecting fetal development and associated with pregnancy complications. In different mouse models in vivo, we demonstrated dramatic embryotoxicity and teratogenicity of increased CypA levels during pregnancy. Using generated transgenic models, we showed that CypA overexpression in fetal tissues induced the death of all transgenic fetuses and complete miscarriage. Administration of recombinant human CypA in a high dose to pregnant females during fetal organogenesis (6.5-11.5 dpc) exhibited teratogenic effects, causing severe defects in the brain and bone development that could lead to malformations and postnatal behavioral and cognitive disorders in the offspring. Embryotoxic and teratogenic effects could be mediated by CypA-induced up-regulation of M1 macrophage polarization via activation of the STAT1/3 signaling pathways. Here, we propose secreted CypA as a novel marker of complicated pregnancy and a therapeutic target for the correction of pregnancy complications.

Indexed as

Cyclophilin APregnancy ComplicationsTeratogenesisAnimalsFemaleFetusHumansMiceOrganogenesisPregnancySignal TransductionCyclophilin Acomplicated pregnancyCyclophilin Aembryotoxicityfetal anatomical defectsmiscarriageorganogenesispro-inflammatory factorteratogenicitytransgenic mice

Identifiers

PMID37511039
PMCPMC10380070
OpenAlexW4383954995

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.