Evidence map›Paper›PMID 39686635›Full record

ReviewCurrent medicinal chemistry2025

An Updated Review Deciphering Apigenin Nanostructures as Promising Therapeutic Efficiency in Human Carcinomas.

Fahad Khan, Mir Waqas Alam, Seema Ramniwas, Indra Rautela, Sorabh Lakhanpal, Pratibha Pandey

Abstract readReview
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In one paragraph

Review in Current medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Fahad KhanCenter for Global Health Research Saveetha Medical College, Saveetha Institute of Medical and Technical Sciences, Chennai, India.
Mir Waqas AlamDepartment of Physics, College of Science, King Faisal University, Al Ahsa, 31982, Saudi Arabia.
Seema RamniwasUniversity Centre of Research and Development, University Institute of Biotechnology, Chandigarh University Gharuan, Mohali, Punjab, India.
Indra RautelaSchool of Applied and Life Sciences, Uttaranchal University, Dehradun, India.
Sorabh LakhanpalSchool of Pharmaceutical Sciences, Lovely Professional University, Phagwara, Punjab, India.
Pratibha PandeyCentre for Research Impact and Outcome, Chitkara University Institute of Engineering and Technology, Chitkara University, Rajpura, 140401, India.

Funding

Deanship of Scientific Research, Vice Presidency for Graduate Studies and Scientific Research, King Faisal University, Saudi Arabia KFU242033
6 · The paper itself

Abstract

Apigenin (APG) is being investigated for its potential in treating different forms of cancer. It can regulate many cellular processes, such as cell proliferation, apoptosis, cell cycle arrest, invasion, metastasis, and autophagy, via controlling multiple cellular signaling pathways. In addition, this chemical demonstrates a significant preference for cancer cells over healthy cells. This is a crucial factor when compared to other treatments for cancer. However, apigenin is distinguished by its limited ability to dissolve in water, sluggish absorption when taken orally, rapid metabolism, and strong affinity for binding to plasma proteins. Therefore, oral dosing generally results in low plasma concentrations. Nanotechnology is being developed to address the constraints of pharmacokinetics and physicochemical properties. It offers a precise and regulated method for delivering drugs, enhancing oral absorption, improving their solubility in water, and reducing side effects. The mechanism of action of apigenin has persuaded the scientific community to acknowledge it as an anticancer drug, hence supporting the utility of apigenin nano formulations as a contemporary therapeutic tool. Nonetheless, diverse nanocarriers for apigenin have effectively addressed inadequate water solubility and non-specificity towards target tissues. This review summarizes diverse biological aspects of apigenin and elaborates on the issues associated with using apigenin nanocarriers to enhance its efficacy in human carcinomas. Subsequent in vivo tests showed its capacity to decrease tumor size, prompting further experimentation with human subjects.

Indexed as

Antineoplastic AgentsApigeninCarcinomaNanostructuresNeoplasmsAnimalsCell ProliferationDrug CarriersHumansAntineoplastic AgentsApigeninDrug CarriersApigenindrug delivery.human carcinomasnanoparticlenanotechnologypharmacokinetics

Identifiers

What OpenQuestion holds

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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.