Evidence map›Paper›PMID 36834647›Full record

ArticleInternational journal of molecular sciences2023

The Role of Mitotic Slippage in Creating a "Female Pregnancy-like System" in a Single Polyploid Giant Cancer Cell.

Kristine Salmina, Ninel Miriam Vainshelbaum, Madara Kreishmane, Inna Inashkina, Mark Steven Cragg, Dace Pjanova, Jekaterina Erenpreisa

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 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Special Issue "Advances in Genome Regulation in Cancer".International journal of molecular sciences · 2023
    Article
  7. Review
  8. 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

7 authors at 2 institutions in 2 countries.

Kristine SalminaCancer Research Division, Latvian Biomedical Research and Study Centre, LV-1067 Riga, Latvia.
Ninel Miriam VainshelbaumCancer Research Division, Latvian Biomedical Research and Study Centre, LV-1067 Riga, Latvia.
Madara KreishmaneCancer Research Division, Latvian Biomedical Research and Study Centre, LV-1067 Riga, Latvia.ORCID 0000-0003-3116-0886
Inna InashkinaCancer Research Division, Latvian Biomedical Research and Study Centre, LV-1067 Riga, Latvia.
Mark Steven CraggCentre for Cancer Immunology, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
Dace PjanovaCancer Research Division, Latvian Biomedical Research and Study Centre, LV-1067 Riga, Latvia.ORCID 0000-0002-3993-7939
Jekaterina ErenpreisaCancer Research Division, Latvian Biomedical Research and Study Centre, LV-1067 Riga, Latvia.ORCID 0000-0002-2870-7775
Latvian Biomedical Research and Study Centre · LVUniversity of Southampton · GB

Funding

Cancer Research UK 23669Cancer Research UK 29101Cancer Research UK 29370
6 · The paper itself

Abstract

In our recent work, we observed that triple-negative breast cancer MDA-MB-231 cells respond to doxorubicin (DOX) via "mitotic slippage" (MS), discarding cytosolic damaged DNA during the process that provides their resistance to this genotoxic treatment. We also noted two populations of polyploid giant cells: those budding surviving offspring, versus those reaching huge ploidy by repeated MS and persisting for several weeks. Their separate roles in the recovery from treatment remained unclear. The current study was devoted to characterising the origin and relationship of these two sub-populations in the context of MS. MS was hallmarked by the emergence of nuclear YAP1/OCT4A/MOS/EMI2-positivity featuring a soma-germ transition to the meiotic-metaphase-arrested "maternal germ cell". In silico, the link between modules identified in the inflammatory innate immune response to cytosolic DNA and the reproductive module of female pregnancy (upregulating placenta developmental genes) was observed in polyploid giant cells. Asymmetry of the two subnuclei types, one repairing DNA and releasing buds enriched by CDC42/ACTIN/TUBULIN and the other persisting and degrading DNA in a polyploid giant cell, was revealed. We propose that when arrested in MS, a "maternal cancer germ cell" may be parthenogenetically stimulated by the placental proto-oncogene parathyroid-hormone-like-hormone, increasing calcium, thus creating a "female pregnancy-like" system within a single polyploid giant cancer cell.

Indexed as

NeoplasmsPlacentaDNAFemaleGiant CellsHormonesHumansPolyploidyPregnancyDNAHormonesbuddingcancerfemale pregnancy systeminnate immune responsematernal germ cellmitotic slippageparthenogenesisplacental developmental genespolyploid giant cellresistance to treatmentsoma-germ transition

Identifiers

PMID36834647
PMCPMC9960874
OpenAlexW4319441712

What OpenQuestion holds

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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.