Evidence map›Paper›PMID 37116378›Full record

ArticleColloids and surfaces. B, Biointerfaces2023

Hybrid peptides as platform for synchronized combination therapy.

Elahe Ashrafichoobdar, Tanner Perez, Luladey Ayalew, Venus Gorbanwand, Joel Monroy, Katarzyna Slowinska

Abstract read
In one paragraph

Article in Colloids and surfaces. B, Biointerfaces, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Elahe AshrafichoobdarDepartment of Chemistry and Biochemistry, California State University Long Beach, 1250 Bellflower Blvd, Long Beach, CA 90840, United States.
Tanner PerezDepartment of Chemistry and Biochemistry, California State University Long Beach, 1250 Bellflower Blvd, Long Beach, CA 90840, United States.
Luladey AyalewDepartment of Chemistry and Biochemistry, California State University Long Beach, 1250 Bellflower Blvd, Long Beach, CA 90840, United States.
Venus GorbanwandDepartment of Chemistry and Biochemistry, California State University Long Beach, 1250 Bellflower Blvd, Long Beach, CA 90840, United States.
Joel MonroyDepartment of Chemistry and Biochemistry, California State University Long Beach, 1250 Bellflower Blvd, Long Beach, CA 90840, United States.
Katarzyna SlowinskaDepartment of Chemistry and Biochemistry, California State University Long Beach, 1250 Bellflower Blvd, Long Beach, CA 90840, United States. Electronic address: katarzyna.slowinska@csulb.edu.

Funding

Supplement for CSULB Maximizing Access to Research Careers (MARC) UNDERGRADUATE STUDENT TRAINING IN ACADEMIC RESEARCH (U-STAR)T34GM008074 · NIGMS · CALIFORNIA STATE UNIVERSITY LONG BEACH · PI NARAYANASWAMI, VASANTHY · 1985 to 2022
$4.6M
Undergraduate Research Training Initiative for Student Enhancement (U-RISE) (T34) at CSULBT34GM149378 · NIGMS · CALIFORNIA STATE UNIVERSITY LONG BEACH · PI VASANTHY NARAYANASWAMI · 2023 to 2026
$2.4M
Rigid-rod Peptides as Nanocarriers for Delivery of Cancer DrugsSC3GM099594 · NIGMS · CALIFORNIA STATE UNIVERSITY LONG BEACH · PI SLOWINSKA, KATARZYNA · 2012 to 2021
$872k
NIGMS NIH HHS SC3 GM099594NIGMS NIH HHS T34 GM008074NIGMS NIH HHS T34 GM149378
6 · The paper itself

Abstract

Combination therapy, where two or more therapeutic agents are combined to target different cellular pathways, is an effective tool in cancer treatment but often difficult to execute. Here we present the collagen peptide-based platform that allows for synchronous and colocalized cellular delivery of three different agents. The peptide is a hybrid between collagen and cell penetrating peptide (CPP) that assembles into a heterotrimer helix and forms fully organic, high aspect ratio nanoparticles. The validity of the approach was tested with three chemically different agents (Paclitaxel, Doxorubicin, and 5-Fluorouracil; a combination used in clinical treatment of (ER)-positive and (PR)-positive breast cancer) conjugated to N-terminus of the peptide. The design of this peptide-based drug delivery system provides several advantages: it avoids drug loading problems; removes the need for orthogonal synthesis; and allows for colocalized delivery of up to three drugs (which leads to the same biodistribution for each drug). In addition, hybrid collagen/CPP peptides are known to enhance cellular uptake and improve solubility of drugs. The synergistic effect, in terms of enhanced efficacy, of the Paclitaxel-Doxorubicin-5-Fluorouracil combination was also calculated. We envision self-assembling peptides as a platform for drug codelivery that can be expanded into a library of personalized combinations that may also include other functionalities like targeting or imaging.

Indexed as

Breast NeoplasmsCell-Penetrating PeptidesNanoparticlesCell Line, TumorCollagenDoxorubicinDrug Delivery SystemsFemaleFluorouracilHumansPaclitaxelPeptidesTissue DistributionCell-Penetrating PeptidesCollagenDoxorubicinFluorouracilPaclitaxelPeptidesCodeliveryCombination therapyHeterotrimer peptidesHybrid peptidesPeptide nanoparticle

Identifiers

PMID37116378
PMCPMC10247525

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.