Evidence map›Paper›PMID 37331841›Full record

ReviewSeminars in cell & developmental biology2024

The antagonistic relationship between apoptosis and polyploidy in development and cancer.

Hunter C Herriage, Yi-Ting Huang, Brian R Calvi

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Epithelial cell fusion is required for tissue repair following UV-A irradiation.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

3 authors at 1 institution in 1 country.

Hunter C HerriageDepartment of Biology, Indiana University, Bloomington, IN 47405, USA.
Yi-Ting HuangDepartment of Biology, Indiana University, Bloomington, IN 47405, USA.
Brian R CalviDepartment of Biology, Indiana University, Bloomington, IN 47405, USA. Electronic address: bcalvi@indiana.edu.
Indiana University Bloomington · US

Funding

Polypoid cell cycle regulation and genome instabilityR01GM113107 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI CALVI, BRIAN R · 2015 to 2022
$2.6M
NIGMS NIH HHS R01 GM113107
6 · The paper itself

Abstract

One of the important functions of regulated cell death is to prevent cells from inappropriately acquiring extra copies of their genome, a state known as polyploidy. Apoptosis is the primary cell death mechanism that prevents polyploidy, and defects in this apoptotic response can result in polyploid cells whose subsequent error-prone chromosome segregation are a major contributor to genome instability and cancer progression. Conversely, some cells actively repress apoptosis to become polyploid as part of normal development or regeneration. Thus, although apoptosis prevents polyploidy, the polyploid state can actively repress apoptosis. In this review, we discuss progress in understanding the antagonistic relationship between apoptosis and polyploidy in development and cancer. Despite recent advances, a key conclusion is that much remains unknown about the mechanisms that link apoptosis to polyploid cell cycles. We suggest that drawing parallels between the regulation of apoptosis in development and cancer could help to fill this knowledge gap and lead to more effective therapies.

Indexed as

NeoplasmsPolyploidyApoptosisChromosome SegregationGenomic InstabilityHumansAneuploidyApoptosisEndoreplicationPolyploidyRegulated cell deathTetraploid

Identifiers

PMID37331841
PMCPMC10724375
OpenAlexW4380881794

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.