Evidence map›Paper›PMID 28536009›Full record

ReviewCancer letters2017

Melittin, a major peptide component of bee venom, and its conjugates in cancer therapy.

Islam Rady, Imtiaz A Siddiqui, Mohamad Rady, Hasan Mukhtar

Abstract readReview
In one paragraph

Review in Cancer letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 177 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
177citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

177 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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  6. Review
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  8. Review
  9. In Vitro Antitumor Effects of Melittin Attached to FeMolecules (Basel, Switzerland) · 2026
    Article
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117 more citing papers are in PubMed but not listed here.

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

4 authors.

Islam RadySchool of Medicine and Public Health, Department of Dermatology, University of Wisconsin-Madison, WI 53706, USA; Department of Zoology, Faculty of Science, Al-Azhar University, Cairo, Egypt.
Imtiaz A SiddiquiSchool of Medicine and Public Health, Department of Dermatology, University of Wisconsin-Madison, WI 53706, USA.
Mohamad RadyDepartment of Zoology, Faculty of Science, Al-Azhar University, Cairo, Egypt.
Hasan MukhtarSchool of Medicine and Public Health, Department of Dermatology, University of Wisconsin-Madison, WI 53706, USA. Electronic address: hmukhtar@wisc.edu.

Funding

Skin Diseases Research Center at the University of WisconsinP30AR066524 · NIAMS · UNIVERSITY OF WISCONSIN-MADISON · PI WOOD, GARY S · 2014 to 2018
$2.6M
NIAMS NIH HHS P30 AR066524
6 · The paper itself

Abstract

Melittin (MEL), a major peptide component of bee venom, is an attractive candidate for cancer therapy. This agent has shown a variety of anti-cancer effects in preclinical cell culture and animal model systems. Despite a convincing efficacy data against variety of cancers, its applicability to humans has met with challenges due to several issues including its non-specific cytotoxicity, degradation and hemolytic activity. Several optimization approaches including utilization of nanoparticle based delivery of MEL have been utilized to circumvent the issues. Here, we summarize the current understanding of the anticancer effects of bee venom and MEL on different kinds of cancers. Further, we also present the available information for the possible mechanism of action of bee venom and/or MEL.

Indexed as

AnimalsAntineoplastic AgentsDrug CarriersDrug CompoundingDrug StabilityHumansMelittenNanoparticlesNanotechnologyNeoplasmsSignal TransductionAntineoplastic AgentsDrug CarriersMelittenAnti-cancer effectsBee venomCancer managementMelittinMelittin conjugates

Identifiers

PMID28536009
PMCPMC5682937

What OpenQuestion holds

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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.