Evidence map›Paper›PMID 39327561›Full record

ArticleBMC oral health2024

The anticancer potential of tetrahydrocurcumin-phytosomes against oral carcinoma progression.

Nehal Raouf, Zeinab Elsayed Darwish, Omneya Ramadan, Hebatallah S Barakat, Shimaa A Elbanna, Marwa M Essawy

Abstract read
In one paragraph

Article in BMC oral health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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.

Nehal RaoufDepartment of Oral Pathology, Faculty of Dentistry, Alexandria University, Champollion Street, Elazarita, Alexandria, 21563, Egypt. nehal.allam.dent@alexu.edu.eg.ORCID https://orcid.org/0009-0000-4864-9915
Zeinab Elsayed DarwishDepartment of Oral Pathology, Faculty of Dentistry, Alexandria University, Champollion Street, Elazarita, Alexandria, 21563, Egypt.
Omneya RamadanDepartment of Oral Pathology, Faculty of Dentistry, Alexandria University, Champollion Street, Elazarita, Alexandria, 21563, Egypt.
Hebatallah S BarakatDepartment of Pharmaceutics, Faculty of Pharmacy, Alexandria University, Alexandria, Egypt.
Shimaa A ElbannaDepartment of Pharmaceutics, Faculty of Pharmacy, Alexandria University, Alexandria, Egypt.
Marwa M EssawyDepartment of Oral Pathology, Faculty of Dentistry, Alexandria University, Champollion Street, Elazarita, Alexandria, 21563, Egypt. marwa.morsy@alexu.edu.eg.ORCID https://orcid.org/0000-0002-4781-4293

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHerbal medicine combined with nanotechnology offers an alternative to the increasing burden of surgery and/or chemotherapy, the main therapeutics of oral carcinoma. Phytosomes are nano-vesicular systems formed by the interaction between phospholipids and phyto-active components via hydrogen bonding, exhibiting superior efficacy over pure phytocomponents in drug delivery.

methodsTetrahydrocurcumin (THC)-phytosomes were prepared by thin film hydration method. After characterization, in vitro cytotoxicity, antiproliferative capacity, antioxidant potential and full apoptotic workup were paneled on oral squamous cell carcinoma (SCC4) in comparison with native THC-solution and cisplatin (3.58 µg/mL intravenous injection), as positive controls. In addition, we tested the three medications on normal oral keratinocytes and gingival fibroblasts to attest to their tissue-selectivity.

resultsSuccessful preparation of THC-phytosomes using 1:1 molar ratio of THC to phospholipid exhibited significantly increased aqueous solubility, good colloidal properties, and complete drug release after one hour. On SCC4 cells, THC-phytosomes, at their dose-/time-dependency at ~ 60.06 µg/mL escalated cell percentages in the S-phase with 32.5 ± 6.22% increase, as well as a startling 29.69 ± 2.3% increase in apoptotic population. Depletion of the cell colonies survival to 0.29 ± 0.1% together with restraining the migratory rate by -6.4 ± 6.8% validated THC-phytosomes' antiproliferative capacity. Comparatively, the corresponding results of THC-solution and cisplatin revealed 12.9 ± 0.9% and 25.8 ± 1.1% for apoptosis and 0.9 ± 0.1% and 0.7 ± 0.08% for colony survival fraction, respectively. Furthermore, the nanoformulation exhibited the strongest immuno-positivity to caspase-3, which positively correlated with intense mitochondrial fluorescence by Mitotracker Red, suggesting its implication in the mitochondrial pathway of apoptosis, a finding further explained by the enormously high Bax and caspase-8 expression by RT-qPCR. Finally, the THC groups showed the lowest oxidative stress index, marking their highest free radical-scavenging potential among the test groups.

conclusionsTHC-phytosomes are depicted to be an efficient nanoformulation that enhanced the anticancer efficacy over the free drug counterpart and the conventional chemotherapeutic. Additionally, being selective to cancer cells and less cytotoxic to normal cells makes THC-phytosomes a potential candidate for tissue-targeted therapy.

Indexed as

ApoptosisCarcinoma, Squamous CellCurcuminMouth NeoplasmsAntineoplastic AgentsAntioxidantsCell Line, TumorCell ProliferationCisplatinDisease ProgressionFibroblastsHumansKeratinocytesPhospholipidsPhytosomesAntineoplastic AgentsAntioxidantsCisplatinCurcuminPhospholipidsPhytosomestetrahydrocurcuminBaxCaspaseMitotracker RedS-phaseSquamous cell carcinoma

Identifiers

PMID39327561
PMCPMC11430579

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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.