Evidence map›Paper›PMID 29774075›Full record

ArticleTheranostics2018

Plectin-targeted liposomes enhance the therapeutic efficacy of a PARP inhibitor in the treatment of ovarian cancer.

Siva Sai Krishna Dasa, Galina Diakova, Ryo Suzuki, Anne M Mills, Michael F Gutknecht, Alexander L Klibanov, Jill K Slack-Davis, Kimberly A Kelly

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 72 citations in OpenAlex.

  1. AI-guided design of plectin-1-targetedJournal of nanobiotechnology · 2026
    Article
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  9. Article
  10. Role of plectin and its interacting molecules in cancer.Medical oncology (Northwood, London, England) · 2023
    Review
  11. Article
  12. Current Update on Nanotechnology-Based Approaches in Ovarian Cancer Therapy.Reproductive sciences (Thousand Oaks, Calif.) · 2023
    Review
  13. Article
  14. Review
  15. [Pharmaceutics · 2022
    Article
  16. Article
  17. Susceptibility of cytoskeletal-associated proteins for tumor progression.Cellular and molecular life sciences : CMLS · 2021
    Review
  18. Article
  19. Review
  20. Review
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

8 authors at 1 institution in 2 countries.

Siva Sai Krishna DasaDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.
Galina DiakovaCancer center, University of Virginia, Charlottesville, VA, USA.
Ryo SuzukiDivision of Cardiovascular Medicine, University of Virginia, Charlottesville, VA, USA.
Anne M MillsDepartment of Pathology, University of Virginia, Charlottesville, VA, USA.
Michael F GutknechtDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.
Alexander L KlibanovDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.
Jill K Slack-DavisDepartment of Microbiology, University of Virginia, Charlottesville, VA, USA.
Kimberly A KellyDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.
University of Virginia · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Jay William FOX · 1987 to 2026
$72.1M
Highly Specific and Efficient Vectors for Targeting Pancreatic CancerR01CA168712 · NCI · UNIVERSITY OF VIRGINIA · PI FRENCH, BRENT A, KELLY, KIMBERLY A. · 2014 to 2017
$2.0M
Development of Molecularly Targeted Imaging Agents for Early Detection of PDACR01CA137071 · NCI · UNIVERSITY OF VIRGINIA · PI KELLY, KIMBERLY A. · 2008 to 2012
$1.3M
NCI NIH HHS P30 CA044579NCI NIH HHS R01 CA137071NCI NIH HHS R01 CA168712
6 · The paper itself

Abstract

Advances in genomics and proteomics drive precision medicine by providing actionable genetic alterations and molecularly targeted therapies, respectively. While genomic analysis and medicinal chemistry have advanced patient stratification with treatments tailored to the genetic profile of a patient's tumor, proteomic targeting has the potential to enhance the therapeutic index of drugs like poly(ADP-ribose) polymerase (PARP) inhibitors. PARP inhibitors in breast and ovarian cancer patients with BRCA1/2 mutations have shown promise. About 10% of the patients who received Olaparib (PARP inhibitor) showed adverse side effects including neutropenia, thrombocytopenia and in some cases resulted in myelodysplastic syndrome, indicating that off-target effects were substantial in these patients. Through proteomic analysis, our lab previously identified plectin, a cytolinker protein that mislocalized onto the cell surface during malignant transformation of healthy ovarian tissue. This cancer specific phenotype allowed us to image pancreatic cancer successfully using plectin targeted peptide (PTP) conjugated to nanoparticles or displayed on capsid protein of adeno-associated virus (AAV) particles.

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorCells, CulturedFemaleHumansLiposomesMiceMice, NudeNanoparticlesOvarian NeoplasmsPeptidesPlectinPoly(ADP-ribose) Polymerase InhibitorsProtein BindingAntineoplastic AgentsLiposomesPeptidesPlectinPoly(ADP-ribose) Polymerase Inhibitorsepithelial ovarian cancergenomicspharmacodynamicspharmacokineticsplectinpoly(ADP-ribose) polymeraseproteomicstargeted drug delivery

Identifiers

PMID29774075
PMCPMC5957009
OpenAlexW2802063908

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.