Evidence map›Paper›PMID 36752075›Full record

ArticleDrug delivery2023

SREKA-targeted liposomes for highly metastatic breast cancer therapy.

Balázs Vári, Levente Dókus, Adina Borbély, Anikó Gaál, Diána Vári-Mező, Ivan Ranđelović, Anna Sólyom-Tisza, Zoltán Varga, Norbert Szoboszlai, Gábor Mező and 1 more

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

11 authors at 7 institutions in 1 country.

Balázs VáriNational Institute of Oncology, Department of Experimental Pharmacology, National Tumor Biology Laboratory, Budapest, Hungary.
Levente DókusResearch Group of Peptide Chemistry, Eötvös Loránd Research Network, Budapest, Hungary.
Adina BorbélyFaculty of Science, Institute of Chemistry, Eötvös Loránd University, Budapest, Hungary.
Anikó GaálEötvös, Loránd Research Network, Research Centre for Natural Sciences, Institute of Materials and Environmental Chemistry, Biological Nanochemistry Research Group, Budapest, Hungary.
Diána Vári-MezőNational Institute of Oncology, Department of Experimental Pharmacology, National Tumor Biology Laboratory, Budapest, Hungary.
Ivan RanđelovićNational Institute of Oncology, Department of Experimental Pharmacology, National Tumor Biology Laboratory, Budapest, Hungary.
Anna Sólyom-TiszaDepartment of Tumor Biology, National Korányi Institute of Pulmonology, Budapest, Hungary.
Zoltán VargaEötvös, Loránd Research Network, Research Centre for Natural Sciences, Institute of Materials and Environmental Chemistry, Biological Nanochemistry Research Group, Budapest, Hungary.
Norbert SzoboszlaiFaculty of Science, Institute of Chemistry, Eötvös Loránd University, Budapest, Hungary.
Gábor MezőResearch Group of Peptide Chemistry, Eötvös Loránd Research Network, Budapest, Hungary.
József TóváriNational Institute of Oncology, Department of Experimental Pharmacology, National Tumor Biology Laboratory, Budapest, Hungary.
Eötvös Loránd University · HUSemmelweis University · HUHungarian Research NetworkHUN-REN Research Centre for Natural Sciences · HUInstitute of Materials and Environmental Chemistry · HUNational Institute of Oncology · HUOrszágos Korányi Tbc és Pulmonológiai Intézet · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemotherapy is still a leading therapeutic approach in various tumor types that is often accompanied by a poor prognosis because of metastases. PEGylated liposomes with CREKA targeting moiety are well-known therapeutic agents, especially in highly metastatic experimental models. CREKA specifically targets tumor-associated ECM, which is present at the primary, as well as metastatic tumor sites. To better understand the function of the targeting moieties, we decided to design various liposome formulations with different amounts of targeting moiety attached to their DSPE-PEG molecules. Moreover, a new tumor-homing pentapeptide (SREKA) was designed, and a novel conjugation strategy between SREKA and DSPE-PEGs. First, the

Indexed as

LiposomesNeoplasmsAnimalsCell Line, TumorDrug Delivery SystemsMiceMice, Inbred BALB CPolyethylene GlycolsLiposomesPolyethylene GlycolsnanocarriersSREKA peptideTargeted cancer therapytumor metastasis

Identifiers

PMID36752075
PMCPMC9930758
OpenAlexW4319460786

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.