Evidence map›Paper›PMID 24750110›Full record

ReviewBritish journal of pharmacology2014

Novel therapeutic targets in myeloma bone disease.

S L Webb, C M Edwards

Abstract readReview
In one paragraph

Review in British journal of pharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Management of Myeloma Bone Lesions.International journal of molecular sciences · 2021
    Review
  2. Observational
  3. An Evidence-Based Approach to Myeloma Bone Disease.Current hematologic malignancy reports · 2017
    Review
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

2 authors.

S L WebbNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.
C M Edwards

Funding

Role of the Bone Marrow Microenvironment in the Development of Multiple MyelomaR01CA137116 · NCI · VANDERBILT UNIVERSITY · PI EDWARDS, CLAIRE · 2010 to 2015
$1.2M
NCI NIH HHS R01 CA137116NCI NIH HHS R01-CA137116
6 · The paper itself

Abstract

Multiple myeloma is a neoplastic disorder of plasma cells characterized by clonal proliferation within the bone marrow. One of the major clinical features of multiple myeloma is the destructive osteolytic bone disease that occurs in the majority of patients. Myeloma bone disease is associated with increased osteoclast activity and suppression of osteoblastogenesis. Bisphosphonates have been the mainstay of treatment for many years; however, their use is limited by their inability to repair existing bone loss. Therefore, research into novel approaches for the treatment of myeloma bone disease is of the utmost importance. This review will discuss the current advances in our understanding of osteoclast stimulation and osteoblast suppression mechanisms in myeloma bone disease and the treatments that are under development to target this destructive and debilitating feature of myeloma.

Indexed as

AnimalsBone Density Conservation AgentsBone DiseasesDiphosphonatesHumansImmunologic FactorsMultiple MyelomaProtease InhibitorsSignal TransductionBone Density Conservation AgentsDiphosphonatesImmunologic FactorsProtease Inhibitors

Identifiers

PMID24750110
PMCPMC4128042

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.