Evidence map›Paper›PMID 19228610›Full record

ArticleBlood2009

The role of IGF-1 as a major growth factor for myeloma cell lines and the prognostic relevance of the expression of its receptor.

Anne Catherine Sprynski, Dirk Hose, Laurent Caillot, Thierry Réme, John D Shaughnessy, Bart Barlogie, Anja Seckinger, Jérôme Moreaux, Michael Hundemer, Michel Jourdan and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

80 citing papers in PubMed, 164 citations in OpenAlex.

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  15. Pathogenic signaling in multiple myeloma.Seminars in oncology · 2022
    Article
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20 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

18 authors at 7 institutions in 3 countries.

Anne Catherine SprynskiInserm U847, Montpellier, France.
Dirk Hose
Laurent Caillot
Thierry Réme
John D Shaughnessy
Bart Barlogie
Anja Seckinger
Jérôme Moreaux
Michael Hundemer
Michel Jourdan
Tobias Meissner
Anna Jauch
Karène Mahtouk
Alboukadel Kassambara
Uta Bertsch
Jean François Rossi
Hartmut Goldschmidt
Bernard Klein
Inserm · FRHeidelberg University · DEUniversity Hospital Heidelberg · DEInstitute for Regenerative Medicine & Biotherapy · FRUniversity of Arkansas for Medical Sciences · USHôpital Saint Eloi · FRNational Center for Tumor Diseases · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A plethora of myeloma growth factors (MGFs) has been identified, but their relative importance and cooperation have not been determined. We investigated 5 MGFs (interleukin-6 [IL-6], insulin-like growth factor type 1 [IGF-1], hepatocyte growth factor [HGF], HB-epidermal growth factor [HB-EGF], and a proliferation-inducing ligand [APRIL]) in serum-free cultures of human myeloma cell lines (HMCLs). In CD45(-) HMCLs, an autocrine IGF-1 loop promoted autonomous survival whereas CD45(+) HMCLs could not survive without addition of MGFs, mainly IGF-1 and IL-6. IGF-1 was the major one: its activity was abrogated by an IGF-1R inhibitor only, whereas IL-6, HGF, or HB-EGF activity was inhibited by both IGF-1R- and receptor-specific inhibition. APRIL activity was inhibited by its specific inhibitor only. Of the investigated MGFs and their receptors, only expressions of IGF-1R and IL-6R in multiple myeloma cells (MMCs) of patients delineate a group with adverse prognosis. This is mainly explained by a strong association of IGF-1R and IL-6R expression and t(4;14) translocation, but IGF-1R expression without t(4;14) can also have a poor prognosis. Thus, IGF-1-targeted therapy, eventually in combination with anti-IL-6 therapy, could be promising in a subset of patients with MMCs expressing IGF-1R.

Indexed as

Blotting, WesternCell DivisionCell Line, TumorCell ProliferationCell SurvivalChromosomes, Human, Pair 14Chromosomes, Human, Pair 4Culture Media, Serum-FreeEnzyme-Linked Immunosorbent AssayFlow CytometryHeparin-binding EGF-like Growth FactorHepatocyte Growth FactorHumansImmunoblottingImmunoenzyme TechniquesIn Situ Hybridization, FluorescenceCulture Media, Serum-FreeHBEGF protein, humanHeparin-binding EGF-like Growth FactorHepatocyte Growth FactorHGF protein, humanInsulin-Like Growth Factor IIntercellular Signaling Peptides and ProteinsInterleukin-6Leukocyte Common AntigensReceptor, IGF Type 1Receptors, Interleukin-6Recombinant ProteinsRNA, MessengerTNFSF13 protein, humanTumor Necrosis Factor Ligand Superfamily Member 13

Identifiers

PMID19228610
PMCPMC2691749
OpenAlexW2051019115

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.