Evidence map›Paper›PMID 35954254›Full record

ArticleCells2022

Discovery of Novel HSP27 Inhibitors as Prospective Anti-Cancer Agents Utilizing Computer-Assisted Therapeutic Discovery Approaches.

Haruna Isiyaku Umar, Adeola Temitayo Ajayi, Nobendu Mukerjee, Abdullahi Tunde Aborode, Mohammad Mehedi Hasan, Swastika Maitra, Ridwan O Bello, Hafsat O Alabere, Afees A Sanusi, Olamide O Awolaja and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-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

15 citing papers in PubMed, 24 citations in OpenAlex.

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  6. Enhancing drought tolerance in cauliflower (Frontiers in plant science · 2024
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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

18 authors at 9 institutions in 5 countries.

Haruna Isiyaku UmarDepartment of Biochemistry, Federal University of Technology, Akure PMB 704, Nigeria.ORCID 0000-0001-9427-9804
Adeola Temitayo AjayiDepartment of Biochemistry, Federal University of Technology, Akure PMB 704, Nigeria.
Nobendu MukerjeeDepartment of Microbiology, Ramakrishna Mission Vivekananda Centenary College, Kolkata 700118, India.ORCID 0000-0002-7129-7003
Abdullahi Tunde AborodeHealthy Africans Platform, Research and Development, Ibadan 200001, Nigeria.ORCID 0000-0003-2516-5920
Mohammad Mehedi HasanDepartment of Biochemistry and Molecular Biology, Faculty of Life Science, Mawlana Bhashani Science and Technology University, Tangail 1902, Bangladesh.ORCID 0000-0002-3871-889X
Swastika MaitraDepartment of Microbiology, Adamas University, Kolkata 222001, India.
Ridwan O BelloComputer-Aided Therapeutic Discovery and Design Group, FUTA, Akure PMB 704, Nigeria.ORCID 0000-0002-6095-5883
Hafsat O AlabereComputer-Aided Therapeutic Discovery and Design Group, FUTA, Akure PMB 704, Nigeria.
Afees A SanusiDepartment of Chemistry, Federal University of Technology, Akure 340252, Nigeria.
Olamide O AwolajaDepartment of Biochemistry, Federal University of Technology, Akure PMB 704, Nigeria.ORCID 0000-0002-2519-9488
Mohammed M AlshehriPharmaceutical Care Department, Ministry of National Guard-Health Affairs, Riyadh 11426, Saudi Arabia.ORCID 0000-0002-2041-4695
Prosper O ChukwuemekaComputer-Aided Therapeutic Discovery and Design Group, FUTA, Akure PMB 704, Nigeria.ORCID 0000-0001-8381-2802
Nada H AljarbaDepartment of Biology, College of Science, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh 11671, Saudi Arabia.ORCID 0000-0001-9224-8844
Saad AlkahtaniDepartment of Zoology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Sumira MalikAmity Institute of Biotechnology, Amity University Jharkhand, Ranchi 834001, India.ORCID 0000-0001-5077-1493
Athanasios AlexiouDepartment of Science and Engineering, Novel Global Community Educational Foundation, Hebersham, NSW 2770, Australia.ORCID 0000-0002-2206-7236
Arabinda GhoshMicrobiology Division, Department of Botany, Gauhati University, Guwahati 781014, India.
Md Habibur RahmanDepartment of Global Medical Science, Wonju College of Medicine, Yonsei University, Wonju 26426, South Korea.ORCID 0000-0001-6099-5693
Federal University of Technology · NGAdamas University · INGauhati University · INKing Saud University · SAMawlana Bhashani Science and Technology University · BDNational Guard Health Affairs · SAPrincess Nourah bint Abdulrahman University · SARamakrishna Mission Vivekananda Educational and Research Institute · INYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heat shock protein 27 (HSP27) is a protein that works as a chaperone and an antioxidant and is activated by heat shock, environmental stress, and pathophysiological stress. However, HSP27 dysregulation is a characteristic of many human cancers. HSP27 suppresses apoptosis and cytoskeletal reorganization. As a result, it is recognized as a critical therapeutic target for effective cancer therapy. Despite the effectiveness of multiple HSP27 inhibitors in pre-clinical investigations and clinical trials, no HSP27 inhibitor has progressed to the anticancer phase of the development. These difficulties have mostly been attributable to existing anticancer therapies' inability to target oncogenic HSP27. Highly selective HSP27 inhibitors with higher effective-ness and low toxicity led to the development of combination techniques that include computer-aided assisted therapeutic discovery and design. This study emphasizes the most recent results and roles of HSP27 in cancer and the potential for utilizing an anticancer chemical database to uncover novel compounds to inhibit HSP27.

Indexed as

Antineoplastic AgentsNeoplasmsApoptosisComputersHSP27 Heat-Shock ProteinsHumansAntineoplastic AgentsHSP27 Heat-Shock Proteinsanti-cancer agentanti-cancer resistancecancer therapycomputer-assisted therapeutic discoveryHSP27 inhibitormolecular docking

Identifiers

PMID35954254
PMCPMC9368632
OpenAlexW4289985771

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.