Evidence map›Paper›PMID 35870089›Full record

ArticleMedical oncology (Northwood, London, England)2022

Expression patterns and therapeutic implications of CDK4 across multiple carcinomas: a molecular docking and MD simulation study.

Hina Qayoom, Umar Mehraj, Shazia Sofi, Shariqa Aisha, Abdullah Almilaibary, Mustfa Alkhanani, Manzoor Ahmad Mir

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

11 citing papers in PubMed, 34 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

7 authors at 3 institutions in 2 countries.

Hina Qayoom *Department of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar, J&K, 190006, India.
Umar Mehraj *Department of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar, J&K, 190006, India.
Shazia SofiDepartment of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar, J&K, 190006, India.
Shariqa AishaDepartment of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar, J&K, 190006, India.
Abdullah AlmilaibaryDepartment of Family and Community Medicine, Albaha University, Albaha, 65511, Kingdom of Saudi Arabia.
Mustfa AlkhananiBiology Department, College of Sciences, University of Hafr Al Batin, Hafar Al Batin, 31991, Kingdom of Saudi Arabia.
Manzoor Ahmad MirDepartment of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar, J&K, 190006, India. drmanzoor@kashmiruniversity.ac.in.ORCID http://orcid.org/0000-0003-3297-1402
University of Kashmir · INAl Baha University · SAUniversity of Hafr Al-Batin · SA

Funding

Jammu and Kashmir Science Technology and Innovation Council, Govt of J&K India Grant NO. JKST&IC/SRE/885-87
6 · The paper itself

Abstract

The CDKs are known to play a critical role in cell cycle regulation process. Among the different groups of CDKs, CDK4 overexpression/hyperactivation is found to be present in many cancers and a specific CDK4 inhibitor, palbociclib has been recently approved by the FDA against breast cancer. However, the treatment with palbociclib has shown many associated toxicities such as-anemia, thrombocytopenia, neutropenia, and febrile neutropenia and more. Despite the fact being FDA approved for only breast cancer and no other cancers and CDK4 being overexpressed in multiple cancers. Therefore, we in our study intend to screen two novel CDK4 inhibitors that show considerably less associated toxicities and greater therapeutic implications than palbociclib. We screened the compounds using Lipinski's rule, ADMET analysis and further analyzed the selected compounds using a virtual screening method called molecular docking and validated our results by MD simulation. We studied the expression patterns and prognostic significance of CDK4 across multiple carcinomas by using some database like UALCAN, cBioportal, and KM-Plotter.

Indexed as

Breast NeoplasmsCarcinomaCyclin-Dependent Kinase 4FemaleHumansMolecular Docking SimulationProtein Kinase InhibitorsCDK4 protein, humanCyclin-Dependent Kinase 4Protein Kinase InhibitorsADMETCDK4MD simulationMolecular dockingPalbociclibPan-cancer

Identifiers

PMID35870089
OpenAlexW4286715941

What Socratic 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 Socratic graph.