Evidence map›Paper›PMID 24793310›Full record

ArticleActa pharmacologica Sinica2014

Abrus agglutinin suppresses human hepatocellular carcinoma in vitro and in vivo by inducing caspase-mediated cell death.

Subhadip Mukhopadhyay, Prashanta Kumar Panda, Durgesh Nandini Das, Niharika Sinha, Birendra Behera, Tapas Kumar Maiti, Sujit Kumar Bhutia

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 55 citations in OpenAlex.

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  11. Plant Lectins as Medical Tools against Digestive System Cancers.International journal of molecular sciences · 2017
    Review
  12. Frontiers in pharmacology · 2017
    Article
  13. 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 2 institutions in 1 country.

Subhadip MukhopadhyayDepartment of Life Science, National Institute of Technology, Rourkela, Odisha, India.
Prashanta Kumar PandaDepartment of Life Science, National Institute of Technology, Rourkela, Odisha, India.
Durgesh Nandini DasDepartment of Life Science, National Institute of Technology, Rourkela, Odisha, India.
Niharika SinhaDepartment of Life Science, National Institute of Technology, Rourkela, Odisha, India.
Birendra BeheraDepartment of Biotechnology, Indian Institute of Technology, Kharagpur, West Bengal, India.
Tapas Kumar MaitiDepartment of Biotechnology, Indian Institute of Technology, Kharagpur, West Bengal, India.
Sujit Kumar BhutiaDepartment of Life Science, National Institute of Technology, Rourkela, Odisha, India.
National Institute of Technology Rourkela · INIndian Institute of Technology Kharagpur · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimAbrus agglutinin (AGG) from the seeds of Indian medicinal plant Abrus precatorius belongs to the class II ribosome inactivating protein family. In this study we investigated the anticancer effects of AGG against human hepatocellular carcinoma in vitro and in vivo.

methodsCell proliferation, DNA fragmentation, Annexin V binding, immunocytofluorescence, Western blotting, caspase activity assays and luciferase assays were performed to evaluate AGG in human liver cancer cells HepG2. Immunohistochemical staining and TUNEL expression were studied in tumor samples of HepG2-xenografted nude mice.

resultsAGG induced apoptosis in HepG2 cells in a dose- and time-dependent manner. AGG-treated HepG2 cells demonstrated an increase in caspase 3/7, 8 and 9 activities and a sharp decrease in the Bcl-2/Bax ratio, indicating activation of a caspase cascade. Co-treatment of HepG2 cells with AGG and a caspase inhibitor or treatment of AGG in Bax knockout HepG2 cells decreased the caspase 3/7 activity in comparison to HepG2 cells exposed only to AGG. Moreover, AGG decreased the expression of Hsp90 and suppressed Akt phosphorylation and NF-κB expression in HepG2 cells. Finally, AGG treatment significantly reduced tumor growth in nude mice bearing HepG2 xenografts, increased TUNEL expression and decreased CD-31 and Ki-67 expression compared to levels observed in the untreated control mice bearing HepG2 cells.

conclusionAGG inhibits the growth and progression of HepG2 cells by inducing caspase-mediated cell death. The agglutinin could be an alternative natural remedy for the treatment of human hepatocellular carcinomas.

Indexed as

AbrusAnimalsAntineoplastic Agents, PhytogenicCarcinoma, HepatocellularCaspasesCell DeathHep G2 CellsHumansLiverLiver NeoplasmsMaleMice, NudePlant Lectinsabrus agglutininAntineoplastic Agents, PhytogenicCaspasesPlant Lectins

Identifiers

PMID24793310
PMCPMC4086388
OpenAlexW2085760513

What OpenQuestion holds

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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.