Evidence map›Paper›PMID 31337024›Full record

ArticleMolecules (Basel, Switzerland)2019

Zerumbone Induces Apoptosis in Breast Cancer Cells by Targeting αvβ3 Integrin upon Co-Administration with TP5-iRGD Peptide.

Eltayeb E M Eid, Abdulrahman S Alanazi, Sanaz Koosha, Alian A Alrasheedy, Faizul Azam, Ismail M Taban, Habibullah Khalilullah, Mothanna Sadiq Al-Qubaisi, Mohammed A Alshawsh

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-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

9 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Bioorthogonal PROTAC Prodrugs Enabled by On-Target Activation.Journal of the American Chemical Society · 2023
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Inclusion complex of clausenidin with hydroxypropyl-β-cyclodextrin: Improved physicochemical properties and anti-colon cancer activity.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2021
    Article
  9. 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

9 authors at 5 institutions in 3 countries.

Eltayeb E M EidDepartment of Pharmaceutical Chemistry and Pharmacognosy, Unaizah College of Pharmacy, Qassim University, 51911 Unaizah, Saudi Arabia. eem.eid@qu.edu.sa.
Abdulrahman S AlanaziCollege of Pharmacy, Hail University, Hail, Saudi Arabia.
Sanaz KooshaDepartment of Pharmacology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.
Alian A AlrasheedyDepartment of Pharmaceutical Chemistry and Pharmacognosy, Unaizah College of Pharmacy, Qassim University, 51911 Unaizah, Saudi Arabia.ORCID 0000-0003-3617-7425
Faizul AzamDepartment of Pharmaceutical Chemistry and Pharmacognosy, Unaizah College of Pharmacy, Qassim University, 51911 Unaizah, Saudi Arabia.ORCID 0000-0002-2927-8167
Ismail M TabanSchool of Biosciences, Cardiff University, Cardiff CF10 3AT, UK.
Habibullah KhalilullahDepartment of Pharmaceutical Chemistry and Pharmacognosy, Unaizah College of Pharmacy, Qassim University, 51911 Unaizah, Saudi Arabia.
Mothanna Sadiq Al-QubaisiInstitute of Bioscience, University Putra Malaysia, 43400 UPM Serdang, Malaysia.
Mohammed A AlshawshDepartment of Pharmacology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia. alshaweshmam@um.edu.my.ORCID 0000-0001-8342-5183
Qassim University · SAUniversity of Malaya · MYCardiff University · GBUniversiti Putra Malaysia · MYUniversity of Ha'il · SA

Funding

Qassim University phuc-2016-1-12-S-1564
6 · The paper itself

Abstract

Cell-penetrating peptides (CPPs) are highly promising tools to deliver therapeutic molecules into tumours. αVβ3 integrins are cell-matrix adhesion receptors, and are considered as an attractive target for anticancer therapies owing to their roles in the process of metastasis and angiogenesis. Therefore, this study aims to assess the effect of co-administration of zerumbone (ZER) and ZERencapsulated in hydroxypropyl-β-cyclodextrin with TP5-iRGD peptide towards cell cytotoxicity, apoptosis induction, and proliferation of normal and cancerous breast cells utilizing in vitro assays, as well as to study the molecular docking of ZER in complex with TP5-iRGD peptide. Cell viability assay findings indicated that ZER and ZERencapsulated in hydroxypropyl-β-cyclodextrin (ZER-HPβCD) inhibited the growth of estrogen receptor positivebreast cancer cells (ER

Indexed as

Antineoplastic AgentsApoptosisCell Line, TumorCell ProliferationCell SurvivalDose-Response Relationship, DrugFemaleHumansIntegrin alphaVbeta3Models, MolecularMolecular ConformationOligopeptidesSesquiterpenesAntineoplastic AgentsIntegrin alphaVbeta3N-end cysteine peptide tumor-homing peptideOligopeptidesSesquiterpeneszerumbonebreast cancerintegrinTP5-iRGD peptidezerumbone

Identifiers

PMID31337024
PMCPMC6680663
OpenAlexW2958846431

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.