Evidence map›Paper›PMID 25364905›Full record

ArticlePloS one2014

Sclerotium rolfsii lectin induces stronger inhibition of proliferation in human breast cancer cells than normal human mammary epithelial cells by induction of cell apoptosis.

Mohammed Azharuddin Savanur, Sachin M Eligar, Radha Pujari, Chen Chen, Pravin Mahajan, Anita Borges, Padma Shastry, Arvind Ingle, Rajiv D Kalraiya, Bale M Swamy and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 33 citations in OpenAlex.

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  11. Lectins with potential for anti-cancer therapy.Molecules (Basel, Switzerland) · 2015
    Review
  12. Article
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

13 authors at 5 institutions in 2 countries.

Mohammed Azharuddin SavanurDepartment of Studies in Biochemistry, Karnatak University, Dharwad, India; Department of Gastroenterology, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Sachin M EligarDepartment of Studies in Biochemistry, Karnatak University, Dharwad, India; Department of Gastroenterology, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Radha PujariNational Centre for Cell Science, NCCS complex, Ganeshkhind, Pune, India.
Chen ChenDepartment of Gastroenterology, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Pravin MahajanS. L. Raheja Hospital, Mahim, Mumbai, India.
Anita BorgesS. L. Raheja Hospital, Mahim, Mumbai, India.
Padma ShastryNational Centre for Cell Science, NCCS complex, Ganeshkhind, Pune, India.
Arvind IngleAdvanced Centre for Treatment, Research and Education in Cancer, Kharghar, Navi Mumabi, India.
Rajiv D KalraiyaAdvanced Centre for Treatment, Research and Education in Cancer, Kharghar, Navi Mumabi, India.
Bale M SwamyDepartment of Studies in Biochemistry, Karnatak University, Dharwad, India; Department of Gastroenterology, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Jonathan M RhodesDepartment of Gastroenterology, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Lu-Gang YuDepartment of Gastroenterology, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Shashikala R InamdarDepartment of Studies in Biochemistry, Karnatak University, Dharwad, India; Department of Gastroenterology, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
University of Liverpool · GBAdvanced Centre for Treatment, Research and Education in Cancer · INNational Centre for Cell Science · INS.L. Raheja Hospital · INKarnatak University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sclerotium rolfsii lectin (SRL) isolated from the phytopathogenic fungus Sclerotium rolfsii has exquisite binding specificity towards O-linked, Thomsen-Freidenreich (Galβ1-3GalNAcα1-Ser/Thr, TF) associated glycans. This study investigated the influence of SRL on proliferation of human breast cancer cells (MCF-7 and ZR-75), non-tumorigenic breast epithelial cells (MCF-10A) and normal mammary epithelial cells (HMECs). SRL caused marked, dose-dependent, inhibition of proliferation of MCF-7 and ZR-75 cells but only weak inhibition of proliferation of non-tumorigenic MCF-10A and HMEC cells. The inhibitory effect of SRL on cancer cell proliferation was shown to be a consequence of SRL cell surface binding and subsequent induction of cellular apoptosis, an effect that was largely prevented by the presence of inhibitors against caspases -3, -8, or -9. Lectin histochemistry using biotin-labelled SRL showed little binding of SRL to normal human breast tissue but intense binding to cancerous tissues. In conclusion, SRL inhibits the growth of human breast cancer cells via induction of cell apoptosis but has substantially less effect on normal epithelial cells. As a lectin that binds specifically to a cancer-associated glycan, has potential to be developed as an anti-cancer agent.

Indexed as

ApoptosisBasidiomycotaBreast NeoplasmsCell Line, TumorCell MembraneCell ProliferationEpithelial CellsFemaleHumansLectinsMammary Glands, HumanProtein BindingLectins

Identifiers

PMID25364905
PMCPMC4217719
OpenAlexW1974856277

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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.