Evidence map›Paper›PMID 16607276›Full record

ArticleOncogene2006

ADAM12 is highly expressed in carcinoma-associated stroma and is required for mouse prostate tumor progression.

L Peduto, V E Reuter, A Sehara-Fujisawa, D R Shaffer, H I Scher, C P Blobel

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 6% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 109 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Depletion of slow-cycling PDGFRαNature immunology · 2023
    Article
  4. Review
  5. Article
  6. Article
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  15. Article
  16. Influence of Immune Myeloid Cells on the Extracellular Matrix During Cancer Metastasis.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2016
    Review
  17. Article
  18. Article
  19. Article
  20. EMMPRIN and ADAM12 in prostate cancer: preliminary results of a prospective study.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    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

6 authors at 3 institutions in 2 countries.

L PedutoGenitourinary Oncology Service, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
V E Reuter
A Sehara-Fujisawa
D R Shaffer
H I Scher
C P Blobel
Memorial Sloan Kettering Cancer Center · USHospital for Special Surgery · USKyoto University · JP

Funding

iRhoms 1 and 2: Key regulators of ADAM17-dependent EGFR signalingR01GM064750 · NIGMS · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI BLOBEL, CARL PETER · 2002 to 2019
$6.1M
EXTRAMURAL RESEARCH FACILITIES CONSTRUCTIONC06RR012538 · NCRR · HOSPITAL FOR SPECIAL SURGERY · PI BOSKEY, ADELE L · 1997 to 1997
–
NCRR NIH HHS C06-RR12538-01NIGMS NIH HHS GM64750
6 · The paper itself

Abstract

The interaction between stromal cells and tumor cells is emerging as a critical aspect of tumor progression. Yet there is a paucity of molecular markers for cells participating in such interactions, and only few genes are known to play a critical role in this process. Here, we describe the identification of ADAM12 (a disintegrin and metalloprotease 12) as a novel marker for a subpopulation of stromal cells that are adjacent to epithelial tumor cells in three mouse carcinoma models (models for prostate, breast and colon cancer). Moreover, we show that ADAM12 is essential for tumor development and progression in the W10 mouse model for prostate cancer. These results suggest that ADAM12 might be a useful marker for stromal cells in mouse tumors that are likely to participate in stromal/tumor cell crosstalk, and that ADAM12 is a potential target for design of drugs that prevent carcinoma growth.

Indexed as

ADAM12 ProteinADAM ProteinsAnimalsAntineoplastic AgentsCell DivisionDisease ProgressionFemaleGene Expression Regulation, NeoplasticIntestinal NeoplasmsMaleMammary Neoplasms, AnimalMiceProstatic NeoplasmsStromal CellsADAM12 ProteinAdam12 protein, mouseADAM ProteinsAntineoplastic Agents

Identifiers

PMID16607276
OpenAlexW2006044964

What OpenQuestion holds

Textmetadata
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.