Evidence map›Paper›PMID 39319107›Full record

ArticleBiomaterials research2024

Advancing Breast Cancer Therapeutics: Targeted Gene Delivery Systems Unveiling the Potential of Estrogen Receptor-Targeting Ligands.

Jung Ro Lee, Young-Min Kim, Eun-Ji Kim, Mi-Kyeong Jang, Seong-Cheol Park

Abstract read
In one paragraph

Article in Biomaterials research, 2024. 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. 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

5 authors.

Jung Ro LeeNational Institute of Ecology (NIE), Seocheon 33657, Korea.
Young-Min KimDepartment of Chemical Engineering, College of Engineering, Sunchon National University, Suncheon, Jeonnam 57922, Korea.
Eun-Ji KimDepartment of Chemical Engineering, College of Engineering, Sunchon National University, Suncheon, Jeonnam 57922, Korea.
Mi-Kyeong JangDepartment of Chemical Engineering, College of Engineering, Sunchon National University, Suncheon, Jeonnam 57922, Korea.
Seong-Cheol ParkDepartment of Chemical Engineering, College of Engineering, Sunchon National University, Suncheon, Jeonnam 57922, Korea.ORCID https://orcid.org/0000-0001-9051-0183

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although curcumin has been well known as a phytochemical drug that inhibits tumor promotion by modulating multiple molecular targets, its potential was not reported as a targeting ligand in the field of drug delivery system. Here, we aimed to assess the tumor-targeting efficiency of curcumin and its derivatives such as phenylalanine, cinnamic acid, coumaric acid, and ferulic acid. Curcumin exhibited a high affinity for estrogen receptors through a pull-down assay using the membrane proteins of MCF-7, a breast cancer cell line, followed by designation of a polymer-based gene therapy system. As a basic backbone for gene binding, dextran grafted with branched polyethylenimine was synthesized, and curcumin and its derivatives were linked to lysine dendrimers. In vitro and in vivo antitumor effects were evaluated using plasmid DNA expressing anti-

Identifiers

PMID39319107
PMCPMC11420687

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.