Evidence map›Paper›PMID 22725698›Full record

ReviewCurrent medicinal chemistry2012

The use of therapeutic peptides to target and to kill cancer cells.

R J Boohaker, M W Lee, P Vishnubhotla, J M Perez, A R Khaled

Abstract readReview
In one paragraph

Review in Current medicinal chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 140 papers.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed
–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

140 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Cytotoxic effects of epsilon toxin fromToxicology research · 2025
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Peptide Fractions Extracted from the Hemolymph ofInternational journal of molecular sciences · 2025
    Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Peptide-Based Therapeutics in Cancer Therapy.Molecular biotechnology · 2024
    Review

80 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

5 authors.

R J BoohakerBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, 6900 Lake Nona Blvd, Orlando, FL 32827, USA.
M W Lee
P Vishnubhotla
J M Perez
A R Khaled

Funding

Identification of regulatory domains that mediate the membrane-binding of BAXR01GM083324 · NIGMS · UNIVERSITY OF CENTRAL FLORIDA · PI KHALED, ANNETTE R · 2008 to 2011
$1.3M
NIGMS NIH HHS GM083324NIGMS NIH HHS R01 GM083324
6 · The paper itself

Abstract

Peptide therapeutics is a promising field for emerging anti-cancer agents. Benefits include the ease and rapid synthesis of peptides and capacity for modifications. An existing and vast knowledge base of protein structure and function can be exploited for novel peptide design. Current research focuses on developing peptides that can (1) serve as tumor targeting moieties and (2) permeabilize membranes with cytotoxic consequences. A survey of recent findings reveals significant trends. Amphiphilic peptides with clusters of hydrophobic and cationic residues are features of anti-microbial peptides that confer the ability to eradicate microbes and show considerable anti-cancer toxicity. Peptides that assemble and form pores can disrupt cell or organelle membranes and cause apoptotic or necrotic death. Cell permeable and tumor-homing peptides can carry biologically active cargo to tumors or tumor vasculature. The challenge lies in developing the clinical application of therapeutic peptides. Improving delivery to tumors, minimizing non-specific toxic effects and discerning pharmacokinetic properties are high among the needs to produce a powerful therapeutic peptide for cancer treatment.

Indexed as

Antimicrobial Cationic PeptidesApoptosisCell-Penetrating PeptidesHumansNeoplasmsPeptide FragmentsPeptidesProto-Oncogene ProteinsAntimicrobial Cationic PeptidesBax protein (53-86)Cell-Penetrating PeptidesPeptide FragmentsPeptidesProto-Oncogene Proteins

Identifiers

PMID22725698
PMCPMC4537071

What OpenQuestion holds

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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.