Evidence map›Paper›PMID 19903879›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

MRPS18-2 protein immortalizes primary rat embryonic fibroblasts and endows them with stem cell-like properties.

Elena Kashuba, Surya Pavan Yenamandra, Suhas Deoram Darekar, Mariya Yurchenko, Vladimir Kashuba, George Klein, Laszlo Szekely

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Review
  2. Cell stemness is maintained upon concurrent expression of RB and the mitochondrial ribosomal protein S18-2.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  3. A novel role for DGATs in cancer.Advances in biological regulation · 2019
    Review
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  6. Article
  7. Review
  8. Article
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  11. Review
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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

7 authors.

Elena KashubaDepartment of Microbiology, Karolinska Institutet, BOX 280, S-17177 Stockholm, Sweden.
Surya Pavan Yenamandra
Suhas Deoram Darekar
Mariya Yurchenko
Vladimir Kashuba
George Klein
Laszlo Szekely

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report that the overexpression of mitochondrial ribosomal protein MRPS18-2 (S18-2) can immortalize primary rat embryonic fibroblasts (REFs). The immortalized cells (18IM) lose contact inhibition, form foci, and are capable of anchorage-independent growth. Concurrently, mesodermal markers, such as vimentin, smooth muscle actin, and Fut4, disappear completely. 18IM cells express embryonic stem cell markers, such as SSEA-1, Sox2, and Oct3/4. In confluent cultures, a portion of cells also express ectoderm- and endoderm-specific pan-keratin, ectoderm-specific beta-III-tubulin, mesoderm-specific MHC class II, and become stainable for fat with Oil red O. None of these changes was detected in c-myc+Ha-ras (MR)-transformed cells. In immunodeficient mice, 18IM cells formed small transiently growing tumors that have down-regulated SSEA-1 and showed pan-keratin staining. We conclude that S18-2 can immortalize REFs and induces them to express stem cell traits.

Indexed as

Cell Transformation, NeoplasticAnimalsBiomarkersCell DifferentiationCells, CulturedCell TransplantationEmbryonic Stem CellsFibroblastsMiceMice, SCIDRatsRecombinant Fusion ProteinsRibosomal ProteinsBiomarkersRecombinant Fusion ProteinsRibosomal Proteinsribosomal protein S18

Identifiers

PMID19903879
PMCPMC2785258

What OpenQuestion holds

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Registered trials

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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.