Evidence map›Paper›PMID 42655920›Full record

ReviewBrain and behavior2026

Natural Compounds Targeting Oncogenic Signaling Networks in Glioblastoma: Molecular Mechanisms, Translational Advances, and Clinical Perspectives.

Mehrukh Zehravi, Md Abul Hassan, Md Al Amin, Sherouk Hussein Sweilam, Jeetendra Kumar Gupta, Ramenani Hari Babu, Pericharla Venkata Narasimha Raju, Krishna Vamsi Kandimalla, Phanindra Erukulla, Patibandla Jahnavi and 4 more

Abstract readReview
In one paragraph

Review in Brain and behavior, 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

14 authors.

Mehrukh ZehraviDepartment of Clinical Pharmacy, College of Dentistry & Pharmacy, Buraydah Private Colleges, Buraydah, Saudi Arabia.
Md Abul HassanNational Research Center For Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Japan.
Md Al AminDepartment of Pharmacy, Faculty of Health and Life Sciences, Daffodil International University, Dhaka, Bangladesh.ORCID https://orcid.org/0009-0009-9924-8674
Sherouk Hussein SweilamDepartment of Pharmacognosy, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia.
Jeetendra Kumar GuptaInstitute of Pharmaceutical Research, GLA University, Mathura, Uttar Pradesh, India.
Ramenani Hari BabuAmity Institute of Pharmacy, Amity University, Gwalior, Madhya Pradesh, India.
Pericharla Venkata Narasimha RajuDepartment of Regulatory Affairs, Hikma Pharmaceuticals USA Inc., Cherry Hill, New Jersey, USA.
Krishna Vamsi KandimallaDepartment of Regulatory Affairs, InvaGen Pharmaceuticals, Central Islip, New York, USA.
Phanindra ErukullaDepartment of Regulatory Affairs, Ricon Pharma LLC, Denville, New Jersey, USA.
Patibandla JahnaviDepartment of Pharmaceutics, KVSR Siddhartha College of Pharmaceutical Sciences, Vijayawada, Andhra Pradesh, India.
Rajeshwar VodetiDepartment of Pharmaceutics, School of Pharmacy, Anurag University, Hyderabad, Telangana, India.
Abdul Ajeed Mohathasim BillahDepartment of Pharmacy Practice, Sri Ramachandra Faculty of Pharmacy, Sri Ramachandra Institute of Higher Education and Research, Chennai, Tamil Nadu, India.
Safia Obaidur RabDepartment of Clinical Laboratory Sciences, College of Applied Medical Science, King Khalid University, Abha, Saudi Arabia.
Sharuk L KhanDepartment of Pharmaceutical Chemistry, N.B.S Institute of Pharmacy, Latur, Maharashtra, India.

Funding

Deanship of Research and Graduate Studies, King Khalid University, Abha, Saudi Arabia R.G.P.2/136/47
6 · The paper itself

Abstract

purposeGlioblastoma (GBM), the most aggressive and common primary brain tumor in adults, has a poor prognosis, rapid growth, and resistance to treatment. Abnormal activation of signaling pathways like PI3K/AKT/mTOR, MAPK/ERK, JAK/STAT, Wnt/β-catenin, NF-κB, and Notch facilitates uncontrolled proliferation, angiogenesis, invasion, and immune evasion. Conventional treatments are insufficient in modifying complex networks, necessitating the urgent need for novel multitargeted treatments. Natural compounds are increasingly being considered as potential treatments for GBM due to their ability to control multiple oncogenic pathways simultaneously and their lower toxicity compared to synthetic medicines. This review provides an integrated and translational perspective on GBM, differing from past reviews that focused on the anticancer effects of individual phytochemicals or specific signaling pathways. We discussed the relationship between natural compounds and key oncogenic signaling networks, focusing on GBM pathogenesis, blood-brain barrier penetration, nanotechnology-assisted delivery, and strategies combining standard therapies. Furthermore, this review critically distinguished in vitro, in vivo, and clinical evidence, focusing on bioavailability challenges, ongoing clinical trials, and future opportunities in precision oncology.

methodTo ensure the inclusion of the most appropriate articles in this review, an in-depth search was carried out on prominent medical, biological, and chemical databases, including Scopus, PubMed, and Web of Science. The search strategy employed combinations of Medical Subject Headings and Boolean operators, focusing on terms related to glioblastoma, natural compounds, and various molecular mechanisms involved in drug delivery, clinical trials, and diagnosis. FINDING: These natural compounds demonstrated potential in preclinical GBM models for inducing apoptosis, suppressing angiogenesis, modulating oxidative stress, and enhancing chemosensitivity. Additionally, some natural compounds can cross the blood-brain barrier, thereby increasing their translational significance. The use of molecular diagnostics, including biomarkers, genetic profiling, and advanced imaging, has significantly improved early identification and patient stratification. Specific compounds with strong translational potential, such as curcumin, resveratrol, EGCG, quercetin, berberine, and luteolin, are highlighted along with their main molecular targets and therapeutic effects. The integration of natural compounds into precision-based therapy approaches has been made possible.

conclusionFuture research aims to combine molecular diagnostics with phytochemical therapies, validate clinical trial outcomes, and enhance bioavailability with nanotechnology delivery systems. The combination of natural compounds shows potential for creating safe, effective, and pathway-specific treatments for GBM.

Indexed as

Biological ProductsBrain NeoplasmsGlioblastomaPhytochemicalsSignal TransductionAnimalsAntineoplastic AgentsHumansAntineoplastic AgentsBiological ProductsPhytochemicalsglioblastomamolecular insightsnatural compoundssignaling pathway

Identifiers

PMID42655920
PMCPMC13519108

What OpenQuestion 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 OpenQuestion graph.