Evidence map›Paper›PMID 8096237›Full record

ArticleThe Journal of experimental medicine1993

A marker for neoplastic progression of human melanocytes is a cell surface ectopeptidase.

M E Morrison, S Vijayasaradhi, D Engelstein, A P Albino, A N Houghton

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 175 citations in OpenAlex.

  1. Review
  2. An Update on Dipeptidyl Peptidase-IV Inhibiting Peptides.Current protein & peptide science · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Depletion of polyfunctional CD26Experimental hematology & oncology · 2023
    Article
  7. CD26 and Cancer.Cancers · 2022
    Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. DPPIV/CD26: a tumor suppressor or a marker of malignancy?Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
  13. Article
  14. Article
  15. DPP4 in Diabetes.Frontiers in immunology · 2015
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Downregulation of Signaling-active IGF-1 by Dipeptidyl Peptidase IV (DPP-IV).International journal of biomedical science : IJBS · 2010
    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

5 authors at 1 institution in 1 country.

M E MorrisonMemorial Sloan-Kettering Cancer Center, New York, New York 10021.
S Vijayasaradhi
D Engelstein
A P Albino
A N Houghton
Memorial Sloan Kettering Cancer Center · US

Funding

CLINICAL SCHOLARS BIOMEDICAL RESEARCH TRAINING PROGRAMT32CA009512 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Ping Chi · 1985 to 2026
$6.3M
ROLE OF ONCOGENES IN THE PATHOGENESIS OF MELANOMAR01CA037907 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI ALBINO, ANTHONY P · 1985 to 1992
–
NCI NIH HHS CA-09512NCI NIH HHS CA-37907
6 · The paper itself

Abstract

Adenosine deaminase binding protein (ADAbp) is a cell surface glycoprotein that is expressed by normal melanocytes but not by melanoma, the malignant counterpart. ADAbp is specifically downregulated during malignant transformation of melanocytes. Recently, we have developed a system that progressively transforms melanocytes in vitro in defined steps. Transduction with v-Ha-ras oncogene followed by long-term culture leads to a cell phenotype and genotype that specifically mimics human melanoma. Loss of ADAbp expression occurred concomitantly with the emergence of growth factor independence and appearance of specific chromosomal abnormalities. The cellular function of ADAbp has not been defined. To characterize ADAbp, the mature 110-kD form was purified from human kidney. Five tryptic peptides from purified human ADAbp revealed 100% homology to a serine protease, human dipeptidyl peptidase IV (DPP IV), also known as CD26. DPP IV activity was detected in lysates from human melanocytes and renal carcinoma cells but not melanoma cells, and DPP IV activity could be specifically isolated from melanocytes by binding to ADA or to S27 monoclonal antibody against ADAbp. These findings show that ADAbp is a cell surface ectopeptidase that is tightly regulated during neoplastic transformation of melanocytes.

Indexed as

Biomarkers, TumorAdenosine DeaminaseAmino Acid SequenceAnimalsCarrier ProteinsCell MembraneCell Transformation, NeoplasticDipeptidyl Peptidase 4Dipeptidyl-Peptidases and Tripeptidyl-PeptidasesGenes, rasHumansMelanocytesMolecular Sequence DataRadioimmunoprecipitation AssaySequence Homology, Amino AcidTumor Cells, CulturedAdenosine DeaminaseBiomarkers, TumorCarrier ProteinsDipeptidyl Peptidase 4Dipeptidyl-Peptidases and Tripeptidyl-Peptidases

Identifiers

PMID8096237
PMCPMC2190962
OpenAlexW2169035807

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.