Evidence map›Paper›PMID 26103567›Full record

ArticlePloS one2015

Analysis of Alpha-2 Macroglobulin from the Long-Lived and Cancer-Resistant Naked Mole-Rat and Human Plasma.

René Thieme, Susanne Kurz, Marlen Kolb, Tewodros Debebe, Susanne Holtze, Michaela Morhart, Klaus Huse, Karol Szafranski, Matthias Platzer, Thomas B Hildebrandt and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Intracellular Signaling Regulated by Activated αInternational journal of molecular sciences · 2026
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  6. Alternative Animal Models of Aging Research.Frontiers in molecular biosciences · 2021
    Review
  7. Toxicological research · 2021
    Article
  8. Review
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  11. Article
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  14. PathogenicFrontiers in microbiology · 2017
    Article
  15. Article
  16. Human plasma protein N-glycosylation.Glycoconjugate journal · 2016
    Review
  17. Article
  18. Article
  19. 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

11 authors at 4 institutions in 1 country.

René ThiemeInstitute of Biochemistry, University of Leipzig, Leipzig, Germany.
Susanne KurzInstitute of Biochemistry, University of Leipzig, Leipzig, Germany.
Marlen KolbInstitute of Biochemistry, University of Leipzig, Leipzig, Germany.
Tewodros DebebeInstitute of Biochemistry, University of Leipzig, Leipzig, Germany.
Susanne HoltzeDepartment of Reproduction Management, Leibniz Institute for Zoo and Wildlife Research, Berlin, Germany.
Michaela MorhartDepartment of Reproduction Management, Leibniz Institute for Zoo and Wildlife Research, Berlin, Germany.
Klaus HuseFritz Lipmann Institute-Leibniz Institute for Age Research, Jena, Germany.
Karol SzafranskiFritz Lipmann Institute-Leibniz Institute for Age Research, Jena, Germany.
Matthias PlatzerFritz Lipmann Institute-Leibniz Institute for Age Research, Jena, Germany.
Thomas B HildebrandtDepartment of Reproduction Management, Leibniz Institute for Zoo and Wildlife Research, Berlin, Germany.
Gerd BirkenmeierInstitute of Biochemistry, University of Leipzig, Leipzig, Germany.
Leipzig University · DELeibniz Institute for Zoo and Wildlife Research · DELeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DELeibniz Association · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe naked mole-rat (NMR) is a long-lived and cancer resistant species. Identification of potential anti-cancer and age related mechanisms is of great interest and makes this species eminent to investigate anti-cancer strategies and understand aging mechanisms. Since it is known that the NMR expresses higher liver mRNA-levels of alpha 2-macroglobulin than mice, nothing is known about its structure, functionality or expression level in the NMR compared to the human A2M.

resultsHere we show a comprehensive analysis of NMR- and human plasma-A2M, showing a different prediction in glycosylation of NMR-A2M, which results in a higher molecular weight compared to human A2M. Additionally, we found a higher concentration of A2M (8.3±0.44 mg/mL vs. and 4.4±0.20 mg/mL) and a lower total plasma protein content (38.7±1.79 mg/mL vs. 61.7±3.20 mg/mL) in NMR compared to human. NMR-A2M can be transformed by methylamine and trypsin resulting in a conformational change similar to human A2M. NMR-A2M is detectable by a polyclonal antibody against human A2M. Determination of tryptic and anti-tryptic activity of NMR and human plasma revealed a higher anti-tryptic activity of the NMR plasma. On the other hand, less proteolytic activity was found in NMR plasma compared to human plasma.

conclusionWe found transformed NMR-A2M binding to its specific receptor LRP1. We could demonstrate lower protein expression of LRP1 in the NMR liver tissue compared to human but higher expression of A2M. This was accompanied by a higher EpCAM protein expression as central adhesion molecule in cancer progression. NMR-plasma was capable to increase the adhesion in human fibroblast in vitro most probably by increasing CD29 protein expression. This is the first report, demonstrating similarities as well as distinct differences between A2M in NMR and human plasma. This might be directly linked to the intriguing phenotype of the NMR and suggests that A2M might probably play an important role in anti-cancer and the anti-aging mechanisms in the NMR.

Indexed as

alpha-MacroglobulinsAnimalsCell Adhesion MoleculesHumansMole RatsNeoplasmsPhylogenyalpha-MacroglobulinsCell Adhesion Molecules

Identifiers

PMID26103567
PMCPMC4477878
OpenAlexW1565471019

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.