Evidence map›Paper›PMID 24767837›Full record

ReviewCancer treatment reviews2014

Recent advances in bone-targeted therapies of metastatic prostate cancer.

Xiyun Deng, Guangchun He, Junwen Liu, Feijun Luo, Xiaoning Peng, Shigang Tang, Zhiyong Gao, Qinlu Lin, Jill M Keller, Tao Yang and 1 more

Abstract readReview
In one paragraph

Review in Cancer treatment reviews, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 58 citations in OpenAlex.

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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

11 authors at 4 institutions in 2 countries.

Xiyun DengCollege of Medicine, Hunan Normal University, Changsha, Hunan 410013, China; Changsha Microworld Biotech Company, Changsha, Hunan 410004, China.
Guangchun HeCollege of Medicine, Hunan Normal University, Changsha, Hunan 410013, China.
Junwen LiuNational Engineering Laboratory for Rice and Byproduct In-Depth Processing, Central South University of Forestry and Technology, Changsha, Hunan 410004, China.
Feijun LuoNational Engineering Laboratory for Rice and Byproduct In-Depth Processing, Central South University of Forestry and Technology, Changsha, Hunan 410004, China.
Xiaoning PengCollege of Medicine, Hunan Normal University, Changsha, Hunan 410013, China.
Shigang TangCollege of Medicine, Hunan Normal University, Changsha, Hunan 410013, China.
Zhiyong GaoCollege of Medicine, Hunan Normal University, Changsha, Hunan 410013, China.
Qinlu LinNational Engineering Laboratory for Rice and Byproduct In-Depth Processing, Central South University of Forestry and Technology, Changsha, Hunan 410004, China.
Jill M KellerDepartment of Urology, University of Michigan, Ann Arbor, MI 48109, USA.
Tao YangNational Engineering Laboratory for Rice and Byproduct In-Depth Processing, Central South University of Forestry and Technology, Changsha, Hunan 410004, China; Changsha Microworld Biotech Company, Changsha, Hunan 410004, China. Electronic address: yangtao807@163.com.
Evan T KellerDepartment of Urology, University of Michigan, Ann Arbor, MI 48109, USA. Electronic address: etkeller@umich.edu.
Hunan Normal University · CNCentral South University of Forestry and Technology · CNUniversity of Michigan–Ann Arbor · USCentral South University · CN

Funding

Tumor microvesicle-mediated modulation of the bone microenvironmentP01CA093900 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KELLER, EVAN T · 2004 to 2024
$29.6M
NCI NIH HHS P01 CA093900
6 · The paper itself

Abstract

Prostate cancer is one of the most common malignancies affecting men worldwide, with bone being the most common site of metastasis in patients that progress beyond organ confinement. Bone metastases are virtually incurable and result in significant disease morbidity and mortality. Bone provides a unique microenvironment whose local interactions with tumor cells offer novel targets for therapeutic interventions. Several attractive molecules or pathways have been identified as new potential therapeutic targets for bone metastases caused by metastatic castration-resistant prostate cancer. In this review, we present the recent advances in molecular targeted therapies for prostate cancer bone metastasis focusing on therapies that target the bone cells and the bone microenvironment. The therapies covered in this review include agents that inhibit bone resorption, agents that stimulate bone formation, and agents that target the bone matrix. Suggestions to devise more effective molecular targeted therapies are proposed. Hopefully, with better understanding of the biology of the disease and the development of more robust targeted therapies, the survival and quality of life of the affected individuals could be significantly improved.

Indexed as

Molecular Targeted TherapyAnimalsAntineoplastic AgentsBone Density Conservation AgentsBone NeoplasmsBone ResorptionCathepsin KDiphosphonatesDisease Models, AnimalHumansMaleOsteogenesisProstatic NeoplasmsRadioisotopesRANK LigandSignal TransductionAntineoplastic AgentsBone Density Conservation AgentsCathepsin KDiphosphonatesRadioisotopesRANK LigandTissue Inhibitor of MetalloproteinasesTNFSF11 protein, humanTransforming Growth Factor betaBone metastasisMolecular targeted therapyOsteoblastsOsteoclastsProstate cancerRANKL

Identifiers

PMID24767837
PMCPMC4042838
OpenAlexW2099790717

What OpenQuestion holds

Textmetadata
LicenceTDM
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.