Cancer is one of the leading causes of death worldwide, affecting millions of people each year. Fortunately, the last decades have been marked by considerable advances in the field of cancer therapy. Researchers have discovered many natural substances, some of which are isolated from plants that have promising anti-tumor activity. Among these, essential oils (EOs) and their constituents have been widely studied and shown potent anticancer activities, both in vitro and in vivo. However, despite the promising results, the precise mechanisms of action of EOs and their bioactive compounds are still poorly understood. Further research is needed to better understand these mechanisms, as well as their effectiveness and safety in use. Furthermore, the use of EOs as anticancer drugs is complex, as it requires absolute pharmacodynamic specificity and selectivity, as well as an appropriate formulation for effective administration. In this study, we present a synthesis of recent work on the mechanisms of anticancer action of EOs and their bioactive compounds, examining the results of various in vitro and in vivo studies. We also review future research prospects in this exciting field, as well as potential implications for the development of new cancer drugs.

The chemical composition of the essential oils of two plants (Tagetes minuta L. and Lavandula coronopifolia L.) harvested from the Day region (in the north of Djibouti) is the subject of this study. The extraction of essential oils was carried out by hydrodistillation, and the average yield was obtained at a rate of approximately 0.25% for Tagetes minuta L. and 0.42% for Lavandula coronopifolia L. The analyses of these essential oils by gas chromatography coupled with mass spectrometry identified 13 compounds in the essential oil of Tagetes minuta L., including dihydrotagetone (20.8%), artemisia (17.9%), (Z)-tagetenone (12.4%), (-)-spathulenol (11.0%) and estragole (9.5%), were obtained as majority compounds, with a percentage of 71.6%. The essential oil of Lavandula coronopifolia L. is characterized by the presence of 42 compounds, including cis-caryophyllene (18.9%), dehydronerolidol (12.8%), isolongifolanone (11.2%), caryophyllene oxide (8.2%), 10-epi-β-eudesmol (7.7%) and humulene (5.1%), were obtained as the majority chemical constituents, with a percentage of 63.9%. The antimicrobial activities of the essential oils at concentrations of 5% were measured against 12 bacterial strains (Gram positive: Staphylococcus aureus (ATCC 29213), Enterococcus faecalis (ATCC 29212), Streptococcus agalactiae (ATCC 27956), Staphylococcus epidermidis and Corynebacterium sp.; Gram Negative: Pseudomonas aeruginosa (ATCC 27853), Escherichia coli (ATCC 25922), Klebsiella pneumoniae (ATCC 700603), Acinetobacter baumannii (ATCC 19606), Shigella sonnei (ATCC 9290), Salmonella enterica sv. Typhimurium (ATCC 13311) and Enterobacter cloacae), and the results of in vitro experiments showed inhibitory effects against most strains tested except Staphylococcus aureus, Enterococcus faecalis and Streptococcus agalactiae. Additionally, both oils were tested for their ability to selectively kill 13 human cancer cells (K562, A549, HCT116, PC3, U87-MG, MIA-Paca2, HEK293, NCI-N87, RT4, U2OS, A2780, MRC-5 and JIMT-T1), and the results obtained, according to the values of IC₅₀, show the significant activity of two essential oils, particularly on the HCT116 and A2780 lines, which present values between 0.25 µg/mL and 0.45 µg/mL, respectively.

Ocimum plants are of great interest to traditional medicine in the history of several civilizations, particularly in terms of chronic human diseases. Essential oils obtained from this genus have also been used as therapeutic agents. In this present work, two plants of the Ocimum species from Djibouti, Ocimum basilicum L. and Ocimum americanum L., were subjected to hydrodistillation to obtain their essential oils. Gas chromatography-mass spectrometry was performed to determine the chemical composition of both essential oils. Linalool (41.2%) and estragole (30.1%) are the major compounds among the 37 compounds that have been identified in the essential oil of Ocimum basilicum L. (EOOB), and carvotanacetol (38.4%) and estragole (27.5%) are the main compounds among the 42 compounds that have been identified in the essential oil of Ocimum americanum L. (EOOA). Morever, the cytotoxic activity of EOs was evaluated against 13 human cancer cell lines (K562, A549, HCT116, PC3, U87-MG, MIA-Paca2, HEK293, NCI-N87, RT4, U2OS, A2780, MRC -5 and JIMT-T1) using a luminescence spectrophotometric method; hence, the oils showed significant cytotoxic activities. The antibacterial activities of the oils were assayed on five Gram-positive bacteria (Staphylococcus aureus, Enterococcus faecalis, Streptococcus agalactiae, Staphylococcus epidermidis and Corynebacterium sp.) and seven Gram-negative bacteria (Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae, Acinetobacter baumannii, Shigella sonnei, Salmonella enterica sv. Typhimurium and Enterobacter cloacae) by agar disc diffusion methods. Both essential oils exhibited moderate activities against Streptococcus agalactiae, and thus each has an activity against Pseudomonas aeruginosa for EOOB and against Enterobacter cloacae for EOOA, while the others are negative. The findings of this work showed the promising anticancer effects of both oils against total cell lines with a potential for use as natural alternatives to synthetic drugs; however, there was only an antibacterial effect against Streptococcus agalactiae.

This work investigates olive pomace from olive mill factories as an adsorbent for the removal of total phenols from olive mill effluent (OME). This pathway of valorization of olive pomace reduces the environmental impact of OME while providing a sustainable and cost-effective wastewater treatment approach for the olive oil industry. Olive pomace was pretreated with water washing, drying (60 °C) and sieving (<2 mm) to obtain the raw olive pomace (OPR) adsorbent material. Olive pomace biochar (OPB) was obtained via carbonization of OPR at 450 °C in a muffle furnace. The adsorbent materials OPR and OPB were characterized using several basic analyzes (Scanning Electron Microscopy–Energy-Dispersive X-ray SEM/EDX, X-ray Diffraction XRD, thermal analysis DTA and TGA, Fourier transform infrared FTIR and Brunauer, Emmett and Teller surface BET). The materials were subsequently tested in a series of experimental tests to optimize the sorption of polyphenols from OME, investigating the effects of pH and adsorbent dose. Adsorption kinetics showed good correlation with a pseudo-second-order kinetic model as well as Langmuir isotherms. Maximum adsorption capacities amounted to 21.27 mg·g⁻¹ for OPR and 66.67 mg·g⁻¹ for OPB, respectively. Thermodynamic simulations indicated spontaneous and exothermic reaction. The rates of total phenol removal were within the range of 10–90% following 24 h batch adsorption in OME diluted at 100 mg/L total phenols, with the highest removal rates observed at pH = 10. Furthermore, solvent regeneration with 70% ethanol solution yielded partial regeneration of OPR at 14% and of OPB at 45% following the adsorption, implying a significant rate of recovery of phenols in the solvent. The results of this study suggest that adsorbents derived from olive pomace may be used as economical materials for the treatment and potential capture of total phenols from OME, also suggesting potential further applications for pollutants in industrial wastewaters, which can have significant implications in the field of environmental technologies.

The aim of this research was to evaluate the essential oils of two medicinal plants from Djibouti: Cymbopogon schoenanthus (L.) Spreng. and Nepeta azurea R.Br. ex Benth. in cytotoxic activity against thirteen (13) cancer cell lines (A2780, A549, HCT116, HEK-293, JIMT-T1, K562, MIA-Paca2, MRC5, NCI-N87, PC3, RT4, U2OS and U87-MG) and antibacterial activity against seven (7) Gram (−) strains (Acinetobacter baumannii, Enterobacter cloacae, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Salmonella enterica sv. Typhimurium and Shigella sonnei) and five (5) Gram (+) strains (Corynebacterium sp., Enterococcus faecalis, Staphylococcus aureus, Staphylococcus epidermidis and Streptococcus agalactiae). The plants were extracted by hydrodistillation and were analyzed by GC-MS. The main components of Cymbopogon schoenanthus essential oil (CSEO) were 3-isopropenyl-5-methyl-1-cyclohexene (32.3%) and D-Limonene (11.3%), and the main component of Nepeta azurea essential oil (NAEO) was methyl (2E)-2-nonenoate (53.2%). The two essential oils showed inhibitory cytotoxicity activities of all the cancer cells tested; on the other hand, the antibacterial activities are only well-noticed for the CSEO oil at a concentration of 5% against Klebsiella pneumoniae, Pseudomonas aeruginosa, Corynebacterium sp., Enterococcus faecalis and Staphylococcus aureus. Our results demonstrated that the two essential oils could be effective natural anticancer agents, in addition to an antibacterial character for Cymbopogon schoenanthus essential oil.