Evidence map›Paper›PMID 37027836›Full record

ArticleHuman reproduction (Oxford, England)2023

The first mitotic division: a perilous bridge connecting the zygote and the early embryo.

Giovanni Coticchio, Danilo Cimadomo, Greta Chiara Cermisoni, Laura Rienzi, Enrico Papaleo, Filippo Maria Ubaldi, Andrea Borini, Lucia De Santis

Open access · hybridAbstract read
In one paragraph

Article in Human reproduction (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Giovanni Coticchio9.baby, GeneraLife IVF, Bologna, Italy.ORCID 0000-0003-1635-9205
Danilo CimadomoClinica Valle Giulia, GeneraLife IVF, Rome, Italy.ORCID 0000-0002-5390-9221
Greta Chiara CermisoniDepartment of Obstetrics/Gynaecology, IVF Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.ORCID 0000-0003-1856-7390
Laura RienziClinica Valle Giulia, GeneraLife IVF, Rome, Italy.ORCID 0000-0001-8104-3958
Enrico PapaleoDepartment of Obstetrics/Gynaecology, IVF Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.ORCID 0000-0003-0281-9143
Filippo Maria UbaldiClinica Valle Giulia, GeneraLife IVF, Rome, Italy.ORCID 0000-0002-6894-2147
Andrea Borini9.baby, GeneraLife IVF, Bologna, Italy.ORCID 0000-0001-9049-0020
Lucia De SantisDepartment of Obstetrics/Gynaecology, IVF Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.ORCID 0000-0001-8540-9988
Clinica Valle Giulia · ITVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human embryos are very frequently affected by maternally inherited aneuploidies, which in the vast majority of cases determine developmental failure at pre- or post-implantation stages. However, recent evidence, generated by the alliance between diverse technologies now routinely employed in the IVF laboratory, has revealed a broader, more complex scenario. Aberrant patterns occurring at the cellular or molecular level can impact at multiple stages of the trajectory of development to blastocyst. In this context, fertilization is an extremely delicate phase, as it marks the transition between gametic and embryonic life. Centrosomes, essential for mitosis, are assembled ex novo from components of both parents. Very large and initially distant nuclei (the pronuclei) are brought together and positioned centrally. The overall cell arrangement is converted from being asymmetric to symmetric. The maternal and paternal chromosome sets, initially separate and scattered within their respective pronuclei, become clustered where the pronuclei juxtapose, to facilitate their assembly in the mitotic spindle. The meiotic spindle is replaced by a segregation machinery that may form as a transient or persistent dual mitotic spindle. Maternal proteins assist the decay of maternal mRNAs to allow the translation of newly synthesized zygotic transcripts. The diversity and complexity of these events, regulated in a precise temporal order and occurring in narrow time windows, make fertilization a highly error-prone process. As a consequence, at the first mitotic division, cellular or genomic integrity may be lost, with fatal consequences for embryonic development.

Indexed as

Cell NucleusZygoteChromosomesEmbryonic DevelopmentFemaleHumansMitosisPregnancySpindle Apparatuschromosomesdevelopmentembryofertilizationoocytepronuclei

Identifiers

PMID37027836
PMCPMC10233254
OpenAlexW4362704431

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.