Evidence map›Paper›PMID 27768593›Full record

ArticleOncotarget2017

Toward the development of a novel non-RGD cyclic peptide drug conjugate for treatment of human metastatic melanoma.

Boris Redko, Helena Tuchinsky, Tamar Segal, Dror Tobi, Galia Luboshits, Osnat Ashur-Fabian, Albert Pinhasov, Gabi Gerlitz, Gary Gellerman

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 38 citations in OpenAlex.

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  11. Anti-Cancer Effects of Cyclic Peptide ALOS4 in a Human Melanoma Mouse Model.International journal of molecular sciences · 2021
    Article
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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

9 authors at 2 institutions in 1 country.

Boris RedkoDepartment of Chemical Sciences, Ariel University, Ariel, Israel.
Helena TuchinskyDepartment of Molecular Biology, Ariel University, Ariel, Israel.
Tamar SegalDepartment of Molecular Biology, Ariel University, Ariel, Israel.
Dror TobiDepartment of Molecular Biology, Ariel University, Ariel, Israel.
Galia LuboshitsDepartment of Chemical Engineering, Ariel University, Ariel, Israel.
Osnat Ashur-FabianDepartment of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Albert PinhasovDepartment of Molecular Biology, Ariel University, Ariel, Israel.
Gabi GerlitzDepartment of Molecular Biology, Ariel University, Ariel, Israel.
Gary GellermanDepartment of Chemical Sciences, Ariel University, Ariel, Israel.
Ariel University · ILTel Aviv University · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The newly discovered short (9 amino acid) non-RGD S-S bridged cyclic peptide ALOS-4 (H-cycl(Cys-Ser-Ser-Ala-Gly-Ser-Leu-Phe-Cys)-OH), which binds to integrin αvβ3 is investigated as peptide carrier for targeted drug delivery against human metastatic melanoma. ALOS4 binds specifically the αvβ3 overexpressing human metastatic melanoma WM-266-4 cell line both in vitro and in ex vivo assays. Coupling ALOS4 to the topoisomerase I inhibitor Camptothecin (ALOS4-CPT) increases the cytotoxicity of CPT against human metastatic melanoma cells while reduces dramatically the cytotoxicity against non-cancerous cells as measured by the levels of γH2A.X, active caspase 3 and cell viability. Moreover, conjugating ALOS4 to CPT even increases the chemo-stability of CPT under physiological pH. Bioinformatic analysis using Rosetta platform revealed potential docking sites of ALOS4 on the αvβ3 integrin which are distinct from the RGD binding sites. We propose to use this specific non-RGD cyclic peptide as the therapeutic carrier for conjugation of drugs in order to improve efficacy and reduce toxicity of currently available treatments of human malignant melanoma.

Indexed as

Drug DiscoveryAnimalsAntineoplastic AgentsCaspase 3Cell Line, TumorCell SurvivalDisease Models, AnimalDNA DamageDrug Evaluation, PreclinicalDrug StabilityHumansIntegrin alphaVbeta3MelanomaMiceModels, MolecularMolecular ConformationAntineoplastic Agentsarginyl-glycyl-aspartic acidCaspase 3Integrin alphaVbeta3OligopeptidesPeptides, Cyclicconjugatehuman metastatic melanomaIntegrin αvβ3non-RGDtargeted drug delivery

Identifiers

PMID27768593
PMCPMC5352194
OpenAlexW2535545817

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.