Evidence map›Paper›PMID 39768856›Full record

ReviewMedicina (Kaunas, Lithuania)2024

TRAIL as a Warrior in Nano-Sized Trojan Horse: Anticancer and Anti-Metastatic Effects of Nano-Formulations of TRAIL in Cell Culture and Animal Model Studies.

Ammad Ahmad Farooqi, Assiya Turgambayeva, Gulnara Kamalbekova, Roza Suleimenova, Natalya Latypova, Sholpan Ospanova, Dinara Ospanova, Zhanat Abdikadyr, Sabit Zhussupov

Abstract readReview
In one paragraph

Review in Medicina (Kaunas, Lithuania), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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.

Ammad Ahmad FarooqiDepartment of Molecular Oncology, Institute of Biomedical and Genetic Engineering (IBGE), Islamabad 44090, Pakistan.ORCID 0000-0003-2209-7483
Assiya TurgambayevaDepartment of Public Health and Management, Astana Medical University, Astana 010000, Kazakhstan.
Gulnara KamalbekovaDepartment of Family Medicine, Astana Medical University, Astana 010000, Kazakhstan.ORCID 0000-0001-9883-6321
Roza SuleimenovaDepartment of Public Health and Hygiene, Astana Medical University, Astana 010000, Kazakhstan.
Natalya LatypovaDepartment of Family Medicine, Astana Medical University, Astana 010000, Kazakhstan.
Sholpan OspanovaDepartment of Public Health and Management, Astana Medical University, Astana 010000, Kazakhstan.
Dinara OspanovaFaculty of Medicine and Healthcare, Al-Farabi Kazakh National University, 71 Al-Farabi Ave, Almaty 050040, Kazakhstan.
Zhanat AbdikadyrDepartment of Biostatistics, Bioinformatics and Information Technologies, Astana Medical University, Astana 010000, Kazakhstan.
Sabit ZhussupovDepartment of Surgery, Semey Medical University, Semey 071400, Kazakhstan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is a therapeutically challenging and genomically complicated disease. Pioneering studies have uncovered multifaceted aspects of cancer, ranging from intra- and inter-tumor heterogeneity, drug resistance, and genetic/epigenetic mutations. Loss of apoptosis is another critical aspect that makes cancer cells resistant to death. A substantial fraction of mechanistic information gleaned from cutting-edge studies has enabled researchers to develop near-to-complete resolution of the apoptotic pathway. Within the exciting frontiers of apoptosis, TRAIL (tumor necrosis factor-related apoptosis-inducing ligand) has garnered phenomenal appreciation by interdisciplinary researchers principally because of its unique capability to target cancer cells. TRAIL-based monotherapies and combinatorial therapies have reached phase II and phase III clinical trials. Rapidly upgrading the list of clinical trials substantiates the clinically valuable role of TRAIL-based therapeutics in cancer therapy. However, there is a growing concern about the poor bioavailability and rapid clearance of TRAIL-based therapeutics. Excitingly, the charismatic field of nanotechnology offers solutions for different problems, and we have witnessed remarkable breakthroughs in the efficacy of TRAIL-based therapeutics using nanotechnological approaches. In this review, we have attempted to provide a summary about different nanotechnologically assisted delivery methods for TRAIL-based therapeutics in cell culture studies and animal model studies for the inhibition/prevention of cancer.

Indexed as

NeoplasmsTNF-Related Apoptosis-Inducing LigandAnimalsAntineoplastic AgentsApoptosisDisease Models, AnimalHumansNanoparticlesAntineoplastic AgentsTNF-Related Apoptosis-Inducing Ligandapoptosiscell signalingmetastasisnano-formulationsnanotechnologyTRAILxenografted mice

Identifiers

PMID39768856
PMCPMC11677168

What OpenQuestion holds

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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.