Evidence map›Paper›PMID 22355275›Full record

ArticleNeoplasia (New York, N.Y.)2012

Inhibition of prostate cancer bone metastasis by synthetic TF antigen mimic/galectin-3 inhibitor lactulose-L-leucine.

Olga V Glinskii, Sudha Sud, Valeri V Mossine, Thomas P Mawhinney, Douglas C Anthony, Gennadi V Glinsky, Kenneth J Pienta, Vladislav V Glinsky

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

44 citing papers in PubMed, 91 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

8 authors at 4 institutions in 1 country.

Olga V GlinskiiDepartment of Medical Pharmacology and Physiology, University of Missouri, Columbia, MO 65212, USA.
Sudha Sud
Valeri V Mossine
Thomas P Mawhinney
Douglas C Anthony
Gennadi V Glinsky
Kenneth J Pienta
Vladislav V Glinsky
University of Missouri · USMichigan Center for Translational Pathology · USSanford Burnham Prebys Medical Discovery Institute · USUniversity of Michigan–Ann Arbor · US

Funding

VACCINIA PSA FOR ANDROGEN-MODULATED POST-SURGICAL RECURRENCE OF PROSTATE CANCERP50CA069568 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COONEY, KATHLEEN A · 1995 to 2013
$31.3M
Tumor microvesicle-mediated modulation of the bone microenvironmentP01CA093900 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PIENTA, KENNETH J. · 2004 to 2024
$29.6M
The Role of Beta-Gal Mediated Interactions in Prostate Cancer MetastasisI01BX000609 · VA · HARRY S. TRUMAN MEMORIAL VA HOSPITAL · PI GLINSKII, VLADISLAV V · 2009 to 2013
–
BLRD VA I01 BX000609NCI NIH HHS 1 P01 CA093900NCI NIH HHS 2 P50 CA69568NCI NIH HHS P01 CA093900NCI NIH HHS P50 CA069568
6 · The paper itself

Abstract

Currently incurable, prostate cancer metastasis has a remarkable ability to spread to the skeleton. Previous studies demonstrated that interactions mediated by the cancer-associated Thomsen-Friedenreich glycoantigen (TF-Ag) and the carbohydrate-binding protein galectin-3 play an important role in several rate-limiting steps of cancer metastasis such as metastatic cell adhesion to bone marrow endothelium, homotypic tumor cell aggregation, and clonogenic survival and growth. This study investigated the ability of a synthetic small-molecular-weight nontoxic carbohydrate-based TF-Ag mimic lactulose-L-leucine (Lac-L-Leu) to inhibit these processes in vitro and, ultimately, prostate cancer bone metastasis in vivo. Using an in vivo mouse model, based on intracardiac injection of human PC-3 prostate carcinoma cells stably expressing luciferase, we investigated the ability of Lac-L-Leu to impede the establishment and growth of bone metastasis. Parallel-flow chamber assay, homotypic aggregation assay, modified Boyden chamber assay, and clonogenic growth assay were used to assess the effects of Lac-L-Leu on tumor cell adhesion to the endothelium, homotypic tumor cell aggregation, transendothelial migration, and clonogenic survival and growth, respectively. We report that daily intraperitoneal administration of Lac-L-Leu resulted in a three-fold (P < .05) decrease in metastatic tumor burden compared with the untreated control. Mechanistically, the effect of Lac-L-Leu, which binds and inhibits galectins by mimicking essential structural features of the TF-Ag, was associated with a dose-dependent inhibition of prostate cancer cell adhesion to bone marrow endothelium, homotypic aggregation, transendothelial migration, and clonogenic growth. We conclude that small-molecular-weight carbohydrate-based compounds targeting β-galactoside-mediated interactions could provide valuable means for controlling and preventing metastatic prostate cancer spread to the skeleton.

Indexed as

Antigens, Tumor-Associated, CarbohydrateAnimalsAntineoplastic AgentsBiomimetic MaterialsBone NeoplasmsCell AdhesionCell Line, TumorCell MovementCell ProliferationCell SurvivalGalectin 3HumansLactuloseLeucineMaleMiceAntigens, Tumor-Associated, CarbohydrateAntineoplastic AgentsGalectin 3LactuloseLeucineThomsen-Friedenreich antigen

Identifiers

PMID22355275
PMCPMC3281943
OpenAlexW1776996595

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.