Evidence map›Paper›PMID 24853427›Full record

ArticleCell death & disease2014

The CT20 peptide causes detachment and death of metastatic breast cancer cells by promoting mitochondrial aggregation and cytoskeletal disruption.

M W Lee, R Bassiouni, N A Sparrow, A Iketani, R J Boohaker, C Moskowitz, P Vishnubhotla, A S Khaled, J Oyer, A Copik and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.5field-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

24 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Anti-cancer peptide-based therapeutic strategies in solid tumors.Cellular & molecular biology letters · 2022
    Article
  6. Article
  7. The TRiCky Business of Protein Folding in Health and Disease.Frontiers in cell and developmental biology · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Mitochondrial Dynamics in Adult Cardiomyocytes and Heart Diseases.Frontiers in cell and developmental biology · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Chaperonin Containing TCP-1 Protein Level in Breast Cancer Cells Predicts Therapeutic Application of a Cytotoxic Peptide.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    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 2 institutions in 1 country.

M W LeeDepartment of Medical Education, College of Medicine, University of Central Florida, Orlando, FL, USA.
R BassiouniBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL, USA.
N A SparrowBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL, USA.
A IketaniBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL, USA.
R J BoohakerBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL, USA.
C MoskowitzDepartment of Medical Education, College of Medicine, University of Central Florida, Orlando, FL, USA.
P VishnubhotlaOrlando Veteran's Administration Medical Center, University of Central Florida, Orlando, FL, USA.
A S KhaledOrlando Veteran's Administration Medical Center, University of Central Florida, Orlando, FL, USA.
J OyerBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL, USA.
A CopikBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL, USA.
C Fernandez-ValleBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL, USA.
J M PerezNanoscience Technology Center, University of Central Florida, Orlando, FL, USA.
A R KhaledBurnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL, USA.
University of Central Florida · USOrlando VA Medical Center · US

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
Mechanisms Modulating Cytoskeletal Dynamics During Schwann Cell MyelinationR01NS062825 · NINDS · UNIVERSITY OF CENTRAL FLORIDA · PI FERNANDEZ-VALLE, CRISTINA MARIA · 2009 to 2010
$722k
NIGMS NIH HHS GM083324NIGMS NIH HHS R01 GM083324NINDS NIH HHS R01 NS062825
6 · The paper itself

Abstract

Metastasis accounts for most deaths from breast cancer, driving the need for new therapeutics that can impede disease progression. Rationally designed peptides that take advantage of cancer-specific differences in cellular physiology are an emerging technology that offer promise as a treatment for metastatic breast cancer. We developed CT20p, a hydrophobic peptide based on the C terminus of Bax that exhibits similarities with antimicrobial peptides, and previously reported that CT20p has unique cytotoxic actions independent of full-length Bax. In this study, we identified the intracellular actions of CT20p which precede cancer cell-specific detachment and death. Previously, we found that CT20p migrated in the heavy membrane fractions of cancer cell lysates. Here, using MDA-MB-231 breast cancer cells, we demonstrated that CT20p localizes to the mitochondria, leading to fusion-like aggregation and mitochondrial membrane hyperpolarization. As a result, the distribution and movement of mitochondria in CT20p-treated MDA-MB-231 cells was markedly impaired, particularly in cell protrusions. In contrast, CT20p did not associate with the mitochondria of normal breast epithelial MCF-10A cells, causing little change in the mitochondrial membrane potential, morphology or localization. In MDA-MB-231 cells, CT20p triggered cell detachment that was preceded by decreased levels of α5β1 integrins and reduced F-actin polymerization. Using folate-targeted nanoparticles to encapsulate and deliver CT20p to murine tumors, we achieved significant tumor regression within days of peptide treatment. These results suggest that CT20p has application in the treatment of metastatic disease as a cancer-specific therapeutic peptide that perturbs mitochondrial morphology and movement ultimately culminating in disruption of the actin cytoskeleton, cell detachment, and loss of cell viability.

Indexed as

Actin CytoskeletonAnimalsAntineoplastic Agentsbcl-2-Associated X ProteinBreast NeoplasmsCell AdhesionCell DeathCell Line, TumorCell SurvivalDrug CarriersFemaleFolic AcidHumansMembrane Potential, MitochondrialMiceMice, NudeAntineoplastic Agentsbcl-2-Associated X ProteinDrug CarriersFolic AcidPeptide Fragments

Identifiers

PMID24853427
PMCPMC4047892
OpenAlexW2003960631

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.