Evidence map›Paper›PMID 42256398›Full record

ReviewFrontiers in pharmacology2026

Exploiting signal transduction pathways for cancer therapy: insights from natural products in preclinical models.

Sarad Pawar Naik Bukke, Balakrishna Vuyyala, Chandrashekar Thalluri, Ananda Kumar Chettupalli, Neha Gupta, Muhammad Ali Abdullah Almoyad, Safa A Abdalla, Vinod Kumar Yata, Alrazi Eisa Shogar, Bayapa Reddy Narapureddy and 3 more

Abstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Sarad Pawar Naik BukkeDepartment of Pharmaceutics and Pharmaceutical Technology, Kampala International University, Kampala, Uganda.
Balakrishna VuyyalaDepartment of Pharmacology, Gurunanak College of Pharmacy, Gurunanak Institutions Technical Campus, Hyderabad, Telangana, India.
Chandrashekar ThalluriFaculty of Pharmaceutical Science, Assam Down Town University (AdtU), Guwahati, Assam, India.
Ananda Kumar ChettupalliDepartment of Pharmaceutical Technology, School of Health and Medical Sciences, Adamas University, Barbaria, West Bengal, India.
Neha GuptaDepartment of Pharmaceutics, Aligarh College of Pharmacy, Aligarh, Uttar Pradesh, India.
Muhammad Ali Abdullah AlmoyadDepartment of Basic Medical Sciences, College of Applied Medical Sciences, Khamis Mushyt, King Khalid University, Abha, Saudi Arabia.
Safa A AbdallaDepartment of Clinical Pharmacy and Pharmacy Practice, Kampala International University, Kampala, Uganda.
Vinod Kumar YataDepartment of Biotechnology, School of Allied and Healthcare Sciences, Malla Reddy University, Hyderabad, Telangana, India.
Alrazi Eisa ShogarDepartment of Clinical Pharmacy and Pharmacy Practice, Kampala International University, Kampala, Uganda.
Bayapa Reddy NarapureddyDepartment of Public Health, College of Applied Medical Sciences, King Khalid University, Abha, Saudi Arabia.
Zohre EftekhariDepartment of Biotechnology, Pasteur Institute of Iran (IPI), Tehran Province, Tehran, Iran.
Patrick Maduabuchi AjaDepartment of Biochemistry, Faculty of Biomedical Sciences, Kampala International University, Kampala, Uganda.
Tadele Mekuriya YadesaDepartment of Clinical Pharmacy and Pharmacy Practice, Kampala International University, Kampala, Uganda.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic or epigenetic changes that lead to abnormal development of signalling through cellular pathways such as MAPK, PI3K/AKT/mTOR, Wnt/β-catenin play an important role in driving cancer. These signalling pathways control how cells grow, divide and die (apoptosis). Thus, the continued activation of these pathways represents a characteristic of oncogenesis as well as a suitable target for treatment. This review will highlight how natural products have been shown to modify the molecular pathways involved with these signalling cascades in preclinical cancer models. Data derived from an array of preclinical studies showcase how the bioactive phytochemicals that comprise these products are implemented in the form of targeting cancer cells through specific inhibition of signalling pathways, induction of apoptosis, inhibition of tumour growth and alteration of oncogenic crosstalk. Despite the significant body of evidence, there are still several limitations that exist in regards to variability between studies in terms of the methods used for validation of the mechanism by which these compounds function, differences in their bioavailability and overall robustness of those studies. Using a pathway-centered understanding of the mechanisms by which natural compounds exert their therapeutic effects will support the development of targeted phytopharmaceutical approaches and promote the integration of these therapies into evidence-based oncology practices.

Indexed as

cancer metabolismmutationsnatural productspreclinical modelssignal transduction pathways

Identifiers

PMID42256398
PMCPMC13237534

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.