Evidence map›Paper›PMID 25364664›Full record

ArticleAdvanced pharmaceutical bulletin2014

Effects of some natural immunomodulatory compounds in combination with thalidomide on survival rate and tumor size in fibrosarcoma-bearing mice.

Reza Aghebati Maleki, Dariush Shanehbandi, Saeed Sadigh Eteghad, Habib Zarredar, Fatemeh Zare Shahneh, Leili Aghebati Maleki, Mehrnosh Samavati, Hamed Asadi, Seyed Ehsan Mosavi, Afshin Habibzadeh and 2 more

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In one paragraph

Article in Advanced pharmaceutical bulletin, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 84% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

12 authors at 2 institutions in 1 country.

Reza Aghebati MalekiHematology and Oncology Research Center, Tabriz University of Medical sciences, Tabriz, Iran.
Dariush ShanehbandiImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Saeed Sadigh EteghadNeurosciences Research Center (NSRC), Tabriz University of Medical Sciences, Tabriz, Iran.
Habib ZarredarImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Fatemeh Zare ShahnehImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Leili Aghebati MalekiImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Mehrnosh SamavatiImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Hamed AsadiHematology and Oncology Research Center, Tabriz University of Medical sciences, Tabriz, Iran.
Seyed Ehsan MosaviHematology and Oncology Research Center, Tabriz University of Medical sciences, Tabriz, Iran.
Afshin HabibzadehHematology and Oncology Research Center, Tabriz University of Medical sciences, Tabriz, Iran.
Mozhdeh MohammadianAmol Faculty of Paramedical Sciences, Mazandaran University of Medical Sciences, Sari, Iran.
Behzad BaradaranImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Tabriz University of Medical Sciences · IRMazandaran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDespite significant advances have been achieved in cancer therapy, response to conventional treatments like surgery, radiotherapy and chemotherapy varies among individuals. Immunotherapy is known to be an effective strategy for patients who are resistant to the currently available interventions.

methodsNinety-six male Balb/c mice (aged 6-8 weeks) were selected and divided into twelve groups of eight. Approximately, 1×10(6)of WEHI-164 cells were injected to each mouse for tumor genesis. Five immunotherapy treatments were considered in this study, including Heat Shock Proteins (HSP), Bacillus Calmette-Guérin (BCG), Bifidobacterium, Immuno-Modulator Drug (IMOD) and Thalidomide. After tumor formation, the groups were treated with one or more of these therapies. Tumor size and survival rate was regularly monitored.

resultsDepending on the treatment group, tumor sizes were different. In some groups, combined treatments demonstrated more inhibitory effects on tumor growth rate. The mice in group (IMOD+ Thalidomide) had the lowest survival rate but group (BCG+ HSP+ Thalidomide) survived until the end of the experiment.

conclusionThe (HSP+ BCG+ Thalidomide) group exhibited satisfactory outcomes and two third of the mice in this group went into complete remission. Some combination therapies in test groups had significant impacts on survival and tumor growth rate.

Indexed as

BCGBifidobacteriumFibrosarcomaHSPIMODThalidomide

Identifiers

PMID25364664
PMCPMC4213787
OpenAlexW2187825363

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Registered trials

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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.