Evidence map›Paper›PMID 27342250›Full record

ArticleJournal of molecular modeling2016

Ligand binding to anti-cancer target CD44 investigated by molecular simulations.

Tin Trung Nguyen, Duy Phuoc Tran, Pham Dinh Quoc Huy, Zung Hoang, Paolo Carloni, Phuc Van Pham, Chuong Nguyen, Mai Suan Li

Abstract read
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In one paragraph

Article in Journal of molecular modeling, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. How Good is Jarzynski's Equality for Computer-Aided Drug Design?The journal of physical chemistry. B · 2020
    Article
  4. Recent Developments and Applications of the MMPBSA Method.Frontiers in molecular biosciences · 2017
    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

8 authors at 5 institutions in 3 countries.

Tin Trung NguyenInstitute for Computational Sciences and Technology, SBI building, Quang Trung Software City, Tan Chanh Hiep Ward, District 12, Ho Chi Minh City, Vietnam.
Duy Phuoc TranUniversity of Technology, Vietnam National University-Ho Chi Minh City, 268 Ly Thuong Kiet Street, District 10, Ho Chi Minh City, Vietnam.
Pham Dinh Quoc HuyInstitute for Computational Sciences and Technology, SBI building, Quang Trung Software City, Tan Chanh Hiep Ward, District 12, Ho Chi Minh City, Vietnam.
Zung HoangCenter for Molecular and NanoArchitecture (MANAR), Vietnam National University-Ho Chi Minh City, Quarter 6, Linh Trung Ward, Thu Duc District, Ho Chi Minh City, Vietnam.
Paolo CarloniComputational Biomedicine, Institute for Advanced Simulation IAS-5 and Institute of Neuroscience and Medicine INM-9, Forschungszentrum Juelich, Juelich, Germany. p.carloni@fz-juelich.de.
Phuc Van PhamStem Cell Research and Application Laboratory, University of Science, Vietnam National University, Ho Chi Minh City, Vietnam. pvphuc@hcmus.edu.vn.
Chuong NguyenTheoretical Physics Research Group, Ton Duc Thang University, Ho Chi Minh City, Vietnam. nguyenhahungchuong@tdt.edu.vn.
Mai Suan LiInstitute of Physics, Polish Academy of Sciences, Al. Lotnikow 32/46, 02-668, Warsaw, Poland. masli@ifpan.edu.pl.
Vietnam National University Ho Chi Minh City · VNPolish Academy of Sciences · PLForschungszentrum Jülich · DEInstitute for Computational Science and Technology · VNTon Duc Thang University · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD44 is a cell-surface glycoprotein and receptor for hyaluronan, one of the major components of the tumor extracellular matrix. There is evidence that the interaction between CD44 and hyaluronan promotes breast cancer metastasis. Recently, the molecule F-19848A was shown to inhibit hyaluronan binding to receptor CD44 in a cell-based assay. In this study, we investigated the mechanism and energetics of F-19848A binding to CD44 using molecular simulation. Using the molecular mechanics/Poisson Boltzmann surface area (MM-PBSA) method, we obtained the binding free energy and inhibition constant of the complex. The van der Waals (vdW) interaction and the extended portion of F-19848A play key roles in the binding affinity. We screened natural products from a traditional Chinese medicine database to search for CD44 inhibitors. From combining pharmaceutical requirements with docking and molecular dynamics simulations, we found ten compounds that are potentially better or equal to the F-19848A ligand at binding to CD44 receptor. Therefore, we have identified new candidates of CD44 inhibitors, based on molecular simulation, which may be effective small molecules for the therapy of breast cancer.

Indexed as

Molecular Dynamics SimulationAntineoplastic AgentsBinding, CompetitiveBinding SitesBreast NeoplasmsHumansHyaluronan ReceptorsHyaluronic AcidHydrogen BondingLigandsMolecular StructureProtein BindingProtein DomainsThermodynamicsAntineoplastic AgentsCD44 protein, humanHyaluronan ReceptorsHyaluronic AcidLigandsBreast cancerCD44F-19848AHyaluronanSteered molecular dynamicsTraditional Chinese medicine

Identifiers

PMID27342250
OpenAlexW2470238647

What OpenQuestion holds

Textmetadata
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.