Evidence map›Paper›PMID 19718049›Full record

ArticleOncogene2009

Bone morphogenic protein 6: a member of a novel class of prognostic factors expressed by normal and malignant plasma cells inhibiting proliferation and angiogenesis.

A Seckinger, T Meissner, J Moreaux, H Goldschmidt, G M Fuhler, A Benner, M Hundemer, T Rème, J D Shaughnessy, B Barlogie and 10 more

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

43 citing papers in PubMed, 77 citations in OpenAlex.

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  9. Morphogens and growth factor signalling in the myeloma bone-lining niche.Cellular and molecular life sciences : CMLS · 2021
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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

20 authors at 8 institutions in 4 countries.

A SeckingerMedizinische Klinik V, Universitätsklinikum Heidelberg, Heidelberg, Germany.
T Meissner
J Moreaux
H Goldschmidt
G M Fuhler
A Benner
M Hundemer
T Rème
J D Shaughnessy
B Barlogie
U Bertsch
J Hillengass
A D Ho
V Pantesco
A Jauch
J De Vos
J F Rossi
T Möhler
B Klein
D Hose
Heidelberg University · DEUniversity Hospital Heidelberg · DEUniversité de Montpellier · FRInserm · FRUniversity of Arkansas for Medical Sciences · USDKFZ-ZMBH Alliance · DEHôpital Saint Eloi · FRUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathogenesis of multiple myeloma is associated with an aberrant expression of pro-proliferative, pro-angiogenic and bone-metabolism-modifying factors by malignant plasma cells. Given the frequently long time span from diagnosis of early-stage plasma cell dyscrasias to overt myeloma and the mostly low proliferation rate of malignant plasma cells, we hypothesize these to similarly express a novel class of inhibitory factors of potential prognostic relevance. Bone morphogenic proteins (BMPs) represent possible candidates as they inhibit proliferation, stimulate bone formation and have an effect on the survival of cancer patients. We assessed the expression of BMPs and their receptors by Affymetrix DNA microarrays (n=779) including CD138-purified primary myeloma cell samples (n=635) of previously untreated patients. BMP6 is the only BMP expressed by malignant and normal plasma cells. Its expression is significantly lower in proliferating myeloma cells, myeloma cell lines or plasmablasts. BMP6 significantly inhibits the proliferation of myeloma cell lines, survival of primary myeloma cells and in vitro angiogenesis. A high BMP6 expression in primary myeloma cell samples delineates significantly superior overall survival for patients undergoing high-dose chemotherapy independent of conventional prognostic factors (International Staging System (ISS) stage, beta(2) microglobulin).

Indexed as

Cell ProliferationGene Expression Regulation, NeoplasticBiomarkers, TumorBone Morphogenetic Protein 6Disease-Free SurvivalFemaleGene Expression ProfilingHumansMaleMultiple MyelomaNeoplasm ProteinsNeovascularization, PathologicOligonucleotide Array Sequence AnalysisPlasma CellsSurvival RateBiomarkers, TumorBMP6 protein, humanBone Morphogenetic Protein 6Neoplasm Proteins

Identifiers

PMID19718049
PMCPMC2844406
OpenAlexW2090826831

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.