Evidence map›Paper›PMID 34641424›Full record

ArticleMolecules (Basel, Switzerland)2021

Computational Screening of Natural Compounds for Identification of Potential Anti-Cancer Agents Targeting MCM7 Protein.

Mohammad Y Alshahrani, Kholoud M Alshahrani, Munazzah Tasleem, Arshiya Akeel, Tahani M Almeleebia, Irfan Ahmad, Mohammed Asiri, Najla A Alshahrani, Nadiyah M Alabdallah, Mohd Saeed

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

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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

10 authors at 5 institutions in 3 countries.

Mohammad Y AlshahraniDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Khalid University, P.O. Box 61413, Abha 62529, Saudi Arabia.ORCID 0000-0002-7096-0221
Kholoud M AlshahraniCollege of Medicine, King Khalid University Abha, P.O. Box 61413, Abha 62529, Saudi Arabia.
Munazzah TasleemSchool of Electronic Science and Engineering, University of Electronic Science and Technology of China, Chengdu 610054, China.ORCID 0000-0002-4811-2154
Arshiya AkeelDepartment of Botany, Aligarh Muslim University, Aligarh 202002, India.ORCID 0000-0002-3068-3768
Tahani M AlmeleebiaDepartment of Clinical Pharmacy, College of Pharmacy, King Khalid University, P.O. Box 61413, Abha 62529, Saudi Arabia.
Irfan AhmadDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Khalid University, P.O. Box 61413, Abha 62529, Saudi Arabia.ORCID 0000-0002-9500-4623
Mohammed AsiriDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Khalid University, P.O. Box 61413, Abha 62529, Saudi Arabia.
Najla A AlshahraniCollege of Medicine, King Khalid University Abha, P.O. Box 61413, Abha 62529, Saudi Arabia.
Nadiyah M AlabdallahDepartment of Biology, College of Science, Imam Abdulrahman Bin Faisal University, P.O. Box 1982, Dammam 31441, Saudi Arabia.
Mohd SaeedDepartment of Biology, College of Sciences, University of Hail, P.O. Box 2440, Hail 55425, Saudi Arabia.
King Khalid University · SAAligarh Muslim University · INImam Abdulrahman Bin Faisal University · SAUniversity of Electronic Science and Technology of China · CNUniversity of Ha'il · SA

Funding

Scientific Research Deanship at King Khalid University and the Ministry of Education in KSA IFP-KKU-2020/14
6 · The paper itself

Abstract

Minichromosome maintenance complex component 7 (MCM7) is involved in replicative licensing and the synthesis of DNA, and its overexpression is a fascinating biomarker for various cancer types. There is currently no effective agent that can prevent the development of cancer caused by the MCM7 protein. However, on the molecular level, inhibiting MCM7 lowers cancer-related cellular growth. With this purpose, this study screened 452 biogenic compounds extracted from the UEFS Natural Products dataset against MCM protein by using the in silico art of technique. The hit compounds UEFS99, UEFS137, and UEFS428 showed good binding with the MCM7 protein with binding energy values of -9.95, -8.92, and -8.71 kcal/mol, which was comparatively higher than that of the control compound ciprofloxacin (-6.50). The hit (UEFS99) with the minimum binding energy was picked for molecular dynamics (MD) simulation investigation, and it demonstrated stability at 30 ns. Computational prediction of physicochemical property evaluation revealed that these hits are non-toxic and have good drug-likeness features. It is suggested that hit compounds UEFS99, UEFS137, and UEFS428 pave the way for further bench work validation in novel inhibitor development against MCM7 to fight the cancers.

Indexed as

Computer SimulationAntineoplastic AgentsBiological ProductsHumansMinichromosome Maintenance Complex Component 7NeoplasmsAntineoplastic AgentsBiological ProductsMCM7 protein, humanMinichromosome Maintenance Complex Component 7cancerDNA synthesisMCM7natural products

Identifiers

PMID34641424
PMCPMC8510405
OpenAlexW3202058468

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.