ReviewFrontiers in oncology2026
Targeted phytotherapy: essential oils, multi-target cancer action & nanodelivery.
Review in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Biochemical components of essential oils (EOs) are an innovative but largely underexplored type of precision phytotherapy (PT) in oncology owing to their anticancer activity against many types of tumors. This article discusses the important multitargeted molecular mechanisms of EOs (apoptosis, cell cycle arrest, angiogenesis, metastasis, tumor microenvironment) and their role as antitumor agents. In particular, an effort has been made to emphasize on the most notable volatile EOs such as thymol, eugenol, limonene, β-caryophyllene, and their interaction with oncogenic signaling pathways (NF-κB, PI3K/AKT/mTOR, MAPK, STAT3). Additionally, the ability of EO constituents to act in synergy with standard chemotherapeutic regimens and immune checkpoint inhibitors are also emphasized. In order to help provide evidence for the anticancer activity of EOs by identifying and examining new nanotechnology-based strategies for drug delivery that address the physicochemical challenges of EOs, this article evaluates advanced nanoformulation techniques, such as lipid-based nanoparticles, polymeric micelles, nanoemulsions, and mesoporous silica carriers. This is discussed in order to define how passive (diffusion) or active (specific targeting) methods can be utilized to improve delivery/absorption. Moreover, this article also discusses EO-derived phytocompounds that can be used in combination with existing chemotherapy or immunotherapy to provide a mechanism(s) to ultimately reverse multidrug resistance. Finally, recent translational bottlenecks before integrating EOs-based PT into precision oncology, such as standardization, regulatory framework, and clinical trials are also addressed.
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What Socratic holds
Registered trials
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.