Evidence map›Paper›PMID 19025658›Full record

ArticleJournal of translational medicine2008

Assessing the clinical utility of measuring Insulin-like Growth Factor Binding Proteins in tissues and sera of melanoma patients.

Jessie Z Yu, Melanie A Warycha, Paul J Christos, Farbod Darvishian, Herman Yee, Hideko Kaminio, Russell S Berman, Richard L Shapiro, Michael T Buckley, Leonard F Liebes and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Functional modulation of IGF-binding protein-3 expression in melanoma.The Journal of investigative dermatology · 2010
    Article
  8. 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

14 authors at 3 institutions in 1 country.

Jessie Z YuDepartment of Dermatology, New York University School of Medicine, New York, NY, USA. yuj05@nyumc.org
Melanie A Warycha
Paul J Christos
Farbod Darvishian
Herman Yee
Hideko Kaminio
Russell S Berman
Richard L Shapiro
Michael T Buckley
Leonard F Liebes
Anna C Pavlick
David Polsky
Peter C Brooks
Iman Osman
New York University · USCornell University · USMaine Medical Center · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
CRYPTIC DOMAINS OF COLLAGEN IV IN TUMOR GROWTHR01CA091645 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BROOKS, PETER C. · 2000 to 2011
$3.3M
NCI NIH HHS 2R01 CA91645NCI NIH HHS 5P30 CA016087-27NCI NIH HHS P30 CA016087NCI NIH HHS R01 CA091645
6 · The paper itself

Abstract

backgroundDifferent Insulin-like Growth Factor Binding Proteins (IGFBPs) have been investigated as potential biomarkers in several types of tumors. In this study, we examined both IGFBP-3 and -4 levels in tissues and sera of melanoma patients representing different stages of melanoma progression.

methodsThe study cohort consisted of 132 melanoma patients (primary, n = 72; metastatic, n = 60; 64 Male, 68 Female; Median Age = 56) prospectively enrolled in the New York University School of Medicine Interdisciplinary Melanoma Cooperative Group (NYU IMCG) between August 2002 and December 2006. We assessed tumor-expression and circulating sera levels of IGFBP-3 and -4 using immunohistochemistry and ELISA assays. Correlations with clinicopathologic parameters were examined using Wilcoxon rank-sum tests and Spearman-rank correlation coefficients.

resultsMedian IGFBP-4 tumor expression was significantly greater in primary versus metastatic patients (70% versus 10%, p = 0.01) A trend for greater median IGFBP-3 sera concentration was observed in metastatic versus primary patients (4.9 microg/ml vs. 3.4 microg/ml, respectively, p = 0.09). However, sera levels fell within a normal range for IGFBP-3. Neither IGFBP-3 nor -4 correlated with survival in this subset of patients.

conclusionDecreased IGFBP-4 tumor expression might be a step in the progression from primary to metastatic melanoma. Our data lend support to a recently-described novel tumor suppressor role of secreting IGFBPs in melanoma. However, data do not support the clinical utility of measuring levels of IGFBP-3 and -4 in sera of melanoma patients.

Indexed as

Biomarkers, TumorDisease ProgressionEnzyme-Linked Immunosorbent AssayFemaleHumansImmunohistochemistryInsulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor Binding Protein 4MaleMelanomaMiddle AgedBiomarkers, TumorInsulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor Binding Protein 4

Identifiers

PMID19025658
PMCPMC2627832
OpenAlexW2106276093

What OpenQuestion holds

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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.