Evidence map›Paper›PMID 28877934›Full record

ArticleGenes & development2017

Identification of senescent cell surface targetable protein DPP4.

Kyoung Mi Kim, Ji Heon Noh, Monica Bodogai, Jennifer L Martindale, Xiaoling Yang, Fred E Indig, Sandip K Basu, Kei Ohnuma, Chikao Morimoto, Peter F Johnson and 3 more

Abstract read
In one paragraph

Article in Genes & development, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 167 papers.

0numbers the graph read from it
0cells of the map it votes in
167citing 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

167 citing papers in PubMed.

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  19. Aging and immunity: the age-old tango.Genes & development · 2025
    Review
  20. Review

107 more citing papers are in PubMed but not listed here.

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

13 authors.

Kyoung Mi KimNational Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, USA.
Ji Heon NohNational Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, USA.
Monica BodogaiNational Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, USA.
Jennifer L MartindaleNational Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, USA.
Xiaoling YangNational Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, USA.
Fred E IndigNational Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, USA.
Sandip K BasuNational Cancer Institute, National Institutes of Health, Frederick, Maryland 21702, USA.
Kei OhnumaGraduate School of Medicine, Juntendo University, Tokyo 113-8421, Japan.
Chikao MorimotoGraduate School of Medicine, Juntendo University, Tokyo 113-8421, Japan.
Peter F JohnsonNational Cancer Institute, National Institutes of Health, Frederick, Maryland 21702, USA.
Arya BiragynNational Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, USA.
Kotb AbdelmohsenNational Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, USA.
Myriam GorospeNational Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, USA.

Funding

Influence of Post-transcriptional Gene Regulation on Cell Senescence and AgingZIAAG000393 · NIA · NATIONAL INSTITUTE ON AGING · PI GOROSPE, MYRIAM · 2009 to 2025
$24.1M
NIA/RRB Confocal Imaging FacilityZICAG000615 · NIA · NATIONAL INSTITUTE ON AGING · PI INDIG, FRED · 2009 to 2025
$17.9M
Role of CEBP transcription factors in regulating cell growth and tumorigenesisZIABC010328 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI JOHNSON, PETER F · 2009 to 2021
$17.5M
Novel immunotherapeutic strategies to treat cancer and diseases of old peopleZIAAG000770 · NIA · NATIONAL INSTITUTE ON AGING · PI BIRAGYN, ARYA · 2009 to 2025
$13.0M
6 · The paper itself

Abstract

Senescent cell accumulation in aging tissues is linked to age-associated diseases and declining function, prompting efforts to eliminate them. Mass spectrometry analysis revealed that DPP4 (dipeptidyl peptidase 4) was selectively expressed on the surface of senescent, but not proliferating, human diploid fibroblasts. Importantly, the differential presence of DPP4 allowed flow cytometry-mediated isolation of senescent cells using anti-DPP4 antibodies. Moreover, antibody-dependent cell-mediated cytotoxicity (ADCC) assays revealed that the cell surface DPP4 preferentially sensitized senescent, but not dividing, fibroblasts to cytotoxicity by natural killer cells. In sum, the selective expression of DPP4 on the surface of senescent cells enables their preferential elimination.

Indexed as

AdultAgedAged, 80 and overAntibody-Dependent Cell CytotoxicityCells, CulturedCellular SenescenceCyclin-Dependent Kinase Inhibitor p16Dipeptidyl Peptidase 4DiploidyFibroblastsFlow CytometryHumansKiller Cells, NaturalLymphocyte SubsetsMass SpectrometryMembrane ProteinsCDKN2A protein, humanCyclin-Dependent Kinase Inhibitor p16Dipeptidyl Peptidase 4DPP4 protein, humanMembrane ProteinsRNA, MessengerRNA, RibosomalCD26cell senescencehuman diploid fibroblasts

Identifiers

PMID28877934
PMCPMC5630018

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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.