Evidence map›Paper›PMID 21765917›Full record

ArticlePloS one2011

Galectin-3C inhibits tumor growth and increases the anticancer activity of bortezomib in a murine model of human multiple myeloma.

Leonardo Mirandola, Yuefei Yu, Kitty Chui, Marjorie R Jenkins, Everardo Cobos, Constance M John, Maurizio Chiriva-Internati

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

35 citing papers in PubMed, 66 citations in OpenAlex.

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  16. Role of MSC-derived galectin 3 in the AML microenvironment.Biochimica et biophysica acta. Molecular cell research · 2018
    Article
  17. Review
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  19. Role of Galectins in Multiple Myeloma.International journal of molecular sciences · 2017
    Review
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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

7 authors at 3 institutions in 1 country.

Leonardo MirandolaDivision of Hematology & Oncology, Texas Tech University Health Sciences Center and Southwest Cancer Treatment and Research Center, Lubbock, Texas, United States of America.
Yuefei Yu
Kitty Chui
Marjorie R Jenkins
Everardo Cobos
Constance M John
Maurizio Chiriva-Internati
Texas Tech University Health Sciences Center · USMandalMed (United States) · USTexas Tech University · US

Funding

Preclinical Testing of Galectin-3C for Multiple MyelomaR43CA135862 · NCI · MANDALMED, INC. · PI CHIRIVA-INTERNATI, MAURIZIO, JOHN, CONSTANCE M · 2008 to 2008
$364k
NCI NIH HHS CA135862-01NCI NIH HHS R43 CA135862
6 · The paper itself

Abstract

Galectin-3 is a human lectin involved in many cellular processes including differentiation, apoptosis, angiogenesis, neoplastic transformation, and metastasis. We evaluated galectin-3C, an N-terminally truncated form of galectin-3 that is thought to act as a dominant negative inhibitor, as a potential treatment for multiple myeloma (MM). Galectin-3 was expressed at varying levels by all 9 human MM cell lines tested. In vitro galectin-3C exhibited modest anti-proliferative effects on MM cells and inhibited chemotaxis and invasion of U266 MM cells induced by stromal cell-derived factor (SDF)-1α. Galectin-3C facilitated the anticancer activity of bortezomib, a proteasome inhibitor approved by the FDA for MM treatment. Galectin-3C and bortezomib also synergistically inhibited MM-induced angiogenesis activity in vitro. Delivery of galectin-3C intravenously via an osmotic pump in a subcutaneous U266 cell NOD/SCID mouse model of MM significantly inhibited tumor growth. The average tumor volume of bortezomib-treated animals was 19.6% and of galectin-3C treated animals was 13.5% of the average volume of the untreated controls at day 35. The maximal effect was obtained with the combination of galectin-3C with bortezomib that afforded a reduction of 94% in the mean tumor volume compared to the untreated controls at day 35. In conclusion, this is the first study to show that inhibition of galectin-3 is efficacious in a murine model of human MM. Our results demonstrated that galectin-3C alone was efficacious in a xenograft mouse model of human MM, and that it enhanced the anti-tumor activity of bortezomib in vitro and in vivo. These data provide the rationale for continued testing of galectin-3C towards initiation of clinical trials for treatment of MM.

Indexed as

Xenograft Model Antitumor AssaysAnimalsAntineoplastic AgentsBoronic AcidsBortezomibCell Line, TumorCell ProliferationCell SurvivalChemotaxisDependovirusDrug SynergismEndothelial CellsFibroblast Growth Factor 2Galectin 3Green Fluorescent ProteinsHumansAntineoplastic AgentsBoronic AcidsBortezomibFibroblast Growth Factor 2Galectin 3Green Fluorescent ProteinsImmunoglobulin EImmunoglobulin lambda-ChainsIntegrin alphaVbeta3PyrazinesVascular Endothelial Growth Factor A

Identifiers

PMID21765917
PMCPMC3135605
OpenAlexW2083689206

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.