Evidence map›Paper›PMID 31820302›Full record

ArticlePathology oncology research : POR2020

In Vivo Tumor Growth Inhibition and Antiangiogenic Effect of Cyclic NGR Peptide-Daunorubicin Conjugates Developed for Targeted Drug Delivery.

Andrea Angelo Pierluigi Tripodi, Ivan Ranđelović, Beáta Biri-Kovács, Bálint Szeder, Gábor Mező, József Tóvári

Open access · hybridAbstract read
In one paragraph

Article in Pathology oncology research : POR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 33 citations in OpenAlex.

  1. Magnetic Hyperthermia via ZnPharmaceutics · 2026
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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 at 3 institutions in 1 country.

Andrea Angelo Pierluigi TripodiMTA-ELTE Research Group of Peptide Chemistry, Hungarian Academy of Sciences, Eötvös Loránd University, Budapest, Hungary.
Ivan RanđelovićDepartment of Experimental Pharmacology, National Institute of Oncology, Budapest, Hungary.
Beáta Biri-KovácsMTA-ELTE Research Group of Peptide Chemistry, Hungarian Academy of Sciences, Eötvös Loránd University, Budapest, Hungary.
Bálint SzederResearch Centre for Natural Sciences, Institute of Enzymology, Hungarian Academy of Sciences, Budapest, Hungary.
Gábor MezőMTA-ELTE Research Group of Peptide Chemistry, Hungarian Academy of Sciences, Eötvös Loránd University, Budapest, Hungary.
József TóváriDepartment of Experimental Pharmacology, National Institute of Oncology, Budapest, Hungary. tozsi@oncol.hu.ORCID http://orcid.org/0000-0002-5543-3204
Eötvös Loránd University · HUNational Institute of Oncology · HUInstitute of Molecular Life Sciences · HU

Funding

European Union and the State of Hungary, co-financed by the European Regional Development Fund VEKOP-2.3.3-15-2017-00020Horizon 2020 642004Nemzeti Kutatási és Technológiai Hivatal NVKP_16-1-2016-0036Nemzeti Kutatási Fejlesztési és Innovációs Hivatal K116295Nemzeti Kutatási Fejlesztési és Innovációs Hivatal NKFIH K119552South Carolina Center of Economic Excellence (US) 1783-3/2018/FEKUTSRATThe 2019 Thematic Excellence Program TUDFO/51757/2019-ITM
6 · The paper itself

Abstract

Among various homing devices, peptides containing the NGR tripeptide sequence represent a promising approach to selectively recognize CD13 receptor isoforms on the surface of tumor cells. They have been successfully used for the delivery of various chemotherapeutic drugs to tumor vessels. Here, we report on the murine plasma stability, in vitro and in vivo antitumor activity of our recently described bioconjugates containing daunorubicin as payload. Furthermore, CD13 expression of KS Kaposi's Sarcoma cell line and HT-29 human colon carcinoma cell line was investigated. Flow cytometry studies confirm the fast cellular uptake resulting in the rapid delivery of the active metabolite Dau = Aoa-Gly-OH to tumor cells. The increased in vitro antitumor effect might be explained by the faster rearrangement from NGR to isoDGR in case of conjugate 2 (Dau = Aoa-GFLGK(c[NleNGRE]-GG)-NH

Indexed as

CD13 AntigensNeoplasms, ExperimentalAnimalsAntibiotics, AntineoplasticCell ProliferationDaunorubicinDrug DiscoveryHumansMiceMice, Inbred BALB CMice, SCIDMolecular Targeted TherapyOligopeptidesPeptides, CyclicXenograft Model Antitumor AssaysAntibiotics, AntineoplasticCD13 AntigensDaunorubicinNGR peptideOligopeptidesPeptides, CyclicAntiangiogenic effectCD13MetastasisNGR peptidesTargeted tumor therapyTumor growth inhibition

Identifiers

PMID31820302
PMCPMC7297862
OpenAlexW2995625337

What OpenQuestion holds

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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.