# Posidonia oceanica (L.) Delile in Focus: In Vitro and In Vivo Evidence for Biomedical Potential

**Authors:** Marzia Vasarri, Lucia De Marchi, Carlo Pretti, Donatella Degl’Innocenti

PMC · DOI: 10.3390/ijms27041727 · International Journal of Molecular Sciences · 2026-02-11

## TL;DR

This paper explores the biomedical potential of Posidonia oceanica, a Mediterranean seagrass, highlighting its bioactive compounds and their effects on health and disease.

## Contribution

The paper provides a comprehensive review of the bioactive properties and delivery technologies of Posidonia oceanica extracts for therapeutic applications.

## Key findings

- Posidonia oceanica contains polyphenols, peptides, and polysaccharides with antioxidant and anti-inflammatory effects.
- In vitro and in vivo studies show its potential in cancer, skin aging, and metabolic disorders.
- Advanced delivery systems enhance the stability and bioavailability of its extracts for pharmaceutical use.

## Abstract

Posidonia oceanica (L.) Delile, an endemic seagrass of the Mediterranean Sea, has been increasingly recognized not only for its ecological significance but also for its potential as a source of bioactive compounds in human health. Over the past decade, scientific studies have identified diverse constituents of P. oceanica, including polyphenols, peptides, and polysaccharides, which exhibit antioxidant, anti-inflammatory, cytotoxic, and metabolic regulatory activities. Evidence from in vitro and in vivo models demonstrates its ability to influence key cellular processes such as apoptosis, autophagy, and enzyme inhibition, suggesting therapeutic promise in cancer, skin aging, inflammatory conditions, and metabolic disorders like type 2 diabetes. Recent advances in delivery technologies, such as nanoparticles, micelles, and liposomes, have improved the stability and bioavailability of P. oceanica extracts, enhancing their potential application in pharmaceuticals and cosmeceuticals. Additionally, its antimicrobial and antibiofilm properties suggest applications in food preservation and infection control. By bridging traditional uses with modern scientific validation, P. oceanica exemplifies the emerging potential of marine phytotherapy. As interest grows in nature-derived therapeutics, further research is essential to translate these preclinical findings into clinical applications while ensuring sustainable management and the conservation of this valuable marine resource.

## Linked entities

- **Diseases:** cancer (MONDO:0004992), type 2 diabetes (MONDO:0005148)
- **Species:** Posidonia oceanica (taxon 55489)

## Full-text entities

- **Genes:** PRDX2 (peroxiredoxin 2) [NCBI Gene 7001] {aka HEL-S-2a, NKEF-B, NKEFB, PRP, PRX2, PRXII}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, Il17a (interleukin 17A) [NCBI Gene 16171] {aka Ctla-8, Ctla8, IL-17, IL-17A, Il17}, Pik3cb (phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit beta) [NCBI Gene 85243], EIF2AK3 (eukaryotic translation initiation factor 2 alpha kinase 3) [NCBI Gene 9451] {aka PEK, PERK, WRS}, BCHE (butyrylcholinesterase) [NCBI Gene 590] {aka BCHED, CHE1, CHE2, E1}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, KDR (kinase insert domain receptor) [NCBI Gene 3791] {aka CD309, FLK1, VEGFR, VEGFR2}, CLDN5 (claudin 5) [NCBI Gene 7122] {aka AWAL, BEC1, CPETRL1, TMDVCF, TMVCF}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}, IRS1 (insulin receptor substrate 1) [NCBI Gene 3667] {aka HIRS-1}, STING1 (stimulator of interferon response cGAMP interactor 1) [NCBI Gene 340061] {aka ERIS, MITA, MPYS, NET23, SAVI, STING}, ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}, MMP2 (matrix metallopeptidase 2) [NCBI Gene 4313] {aka CLG4, CLG4A, MMP-2, MMP-II, MONA, TBE-1}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 17709], TYR (tyrosinase) [NCBI Gene 7299] {aka ATN, CMM8, OCA1, OCA1A, OCAIA, SHEP3}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, SLC2A4 (solute carrier family 2 member 4) [NCBI Gene 6517] {aka GLUT4}, PRKCZ (protein kinase C zeta) [NCBI Gene 5590] {aka PKC-ZETA, PKC2}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, SLC5A1 (solute carrier family 5 member 1) [NCBI Gene 6523] {aka D22S675, NAGT, SGLT-1, SGLT1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, VCAM1 (vascular cell adhesion molecule 1) [NCBI Gene 7412] {aka CD106, INCAM-100}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, FASN (fatty acid synthase) [NCBI Gene 2194] {aka FAS, OA-519, SDR27X1}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, KMT2A (lysine methyltransferase 2A) [NCBI Gene 4297] {aka ALL-1, ALL1, CXXC7, GAS7, HRX, HTRX}, AKR1B10 (aldo-keto reductase family 1 member B10) [NCBI Gene 57016] {aka AKR1B11, AKR1B12, ALDRLn, ARL-1, ARL1, HIS}, MAPK8 (mitogen-activated protein kinase 8) [NCBI Gene 5599] {aka JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, Il23a (interleukin 23, alpha subunit p19) [NCBI Gene 83430] {aka IL-23, p19}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Mpo (myeloperoxidase) [NCBI Gene 17523] {aka mKIAA4033}, SLC2A2 (solute carrier family 2 member 2) [NCBI Gene 6514] {aka GLUT2}, Ptgs2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 19225] {aka COX2, Cox-2, PES-2, PGHS-2, PHS II, PHS-2}, MAPK14 (mitogen-activated protein kinase 14) [NCBI Gene 1432] {aka CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2}, ACHE (acetylcholinesterase (Yt blood group)) [NCBI Gene 43] {aka ACEE, ARACHE, N-ACHE, YT}, AKR1C1 (aldo-keto reductase family 1 member C1) [NCBI Gene 1645] {aka 2-ALPHA-HSD, 20-ALPHA-HSD, DD1, DD1/DD2, DDH, DDH1}, RENBP (renin binding protein) [NCBI Gene 5973] {aka RBP, RNBP}, Lcn2 (lipocalin 2) [NCBI Gene 16819] {aka 24p3, NRL, Sip24}, HMOX1 (heme oxygenase 1) [NCBI Gene 3162] {aka HMOX1D, HO-1, HSP32, bK286B10}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, Nos3 (nitric oxide synthase 3) [NCBI Gene 24600] {aka eNos}, Akt1 (Akt serine/threonine kinase 1) [NCBI Gene 11651] {aka Akt, LTR-akt, PKB, PKB/Akt, PKBalpha, Rac}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** neuroinflammation (MESH:D000090862), hyperkeratosis (MESH:D017488), edema (MESH:D004487), Cancer (MESH:D009369), Diabetes (MESH:D003920), NAFLD (MESH:D065626), fibrosarcoma (MESH:D005354), Alzheimer's disease (MESH:D000544), skin disorders (MESH:D012871), mitochondrial dysfunction (MESH:D028361), hyperpigmentation (MESH:D017495), inflammatory pain (MESH:D010146), melanoma (MESH:D008545), Inflammatory (MESH:D007249), neurodegeneration (MESH:D019636), injury to (MESH:D014947), photo-damage (MESH:D054039), pigmentary disorders (MESH:C535508), neuroblastoma (MESH:D009447), Psoriasis (MESH:D011565), acute (MESH:D000208), Metabolic Disorders (MESH:D008659), insulin resistance (MESH:D007333), cytotoxic (MESH:D064420), vascular dysfunction (MESH:D002561), immune-mediated systemic disease (MESH:D007154), infection (MESH:D007239), death (MESH:D003643), diabetic complications (MESH:D048909), chronic diseases (MESH:D002908), neuropathy (MESH:D009422), intestinal dysfunction (MESH:D007410), hepatocellular carcinoma (MESH:D006528), kidney damage (MESH:D007674), breast cancer (MESH:D001943), type 2 diabetes (MESH:D003924)
- **Chemicals:** rutin (MESH:D012431), carbon (MESH:D002244), ciprofloxacin (MESH:D002939), DPPH (MESH:C004931), prostaglandins (MESH:D011453), polysaccharides (MESH:D011134), gallic acid (MESH:D005707), vanillic acid (MESH:D014641), oxygen (MESH:D010100), sulfate (MESH:D013431), chitosan (MESH:D048271), caffeic acid methyl ester (MESH:C497945), blood glucose (MESH:D001786), NO (MESH:D009569), ethanol (MESH:D000431), sorafenib (MESH:D000077157), resveratrol (MESH:D000077185), p-hydroxybenzoic acid (MESH:C038193), procyanidin (MESH:C017674), catechin (MESH:D002392), quercetin 3-O-galactoside (MESH:C021304), phenolic acids (MESH:C017616), myricetin (MESH:C040015), ferulic acid (MESH:C004999), vanillin (MESH:C100058), galantamine (MESH:D005702), Polydatin (MESH:C058229), phenols (MESH:D010636), delphinidin-3-glucoside (MESH:C494120), alloxan (MESH:D000496), P. oceanica hydroalcoholic extract (-), ROS (MESH:D017382), flavonoids (MESH:D005419), chlorogenic acid (MESH:D002726), Glucose (MESH:D005947), IMQ (MESH:D000077271), caffeic acid (MESH:C040048), ellagic acid (MESH:D004610), p-coumaric acid (MESH:C495469), melanin (MESH:D008543), chicoric acid (MESH:C100435), Lipid (MESH:D008055), LPS (MESH:D008070), erlotinib (MESH:D000069347), polyphenol (MESH:D059808)
- **Species:** Klebsiella pneumoniae (species) [taxon 573], Aspergillus niger (species) [taxon 5061], Pseudomonas aeruginosa (species) [taxon 287], Mus musculus (house mouse, species) [taxon 10090], Agaricus bisporus (common mushroom, species) [taxon 5341], Escherichia coli (E. coli, species) [taxon 562], Enterococcus faecalis (species) [taxon 1351], Penicillium chrysogenum (species) [taxon 5076], Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus aureus (species) [taxon 1280], Rattus norvegicus (brown rat, species) [taxon 10116], Cercopithecidae (monkey, family) [taxon 9527], Posidonia oceanica (species) [taxon 55489]
- **Mutations:** T790M
- **Cell lines:** MeWo — Homo sapiens (Human), Cutaneous melanoma, Cancer cell line (CVCL_0445), HepG2 — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027), 46BR.1N — Homo sapiens (Human), DNA ligase I deficiency, Transformed cell line (CVCL_2289), MCF-7 — Homo sapiens (Human), Invasive breast carcinoma of no special type, Cancer cell line (CVCL_0031), RAW264.7 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_0493), HS-68 — Homo sapiens (Human), Canavan disease, Finite cell line (CVCL_0839), C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU), Caco-2 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0025), HT1080 — Homo sapiens (Human), Fibrosarcoma, Cancer cell line (CVCL_0317), CD-1 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_5731), Vero — Chlorocebus sabaeus (Green monkey), Spontaneously immortalized cell line (CVCL_0059), SH-SY5Y — Homo sapiens (Human), Neuroblastoma, Cancer cell line (CVCL_0019)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940555/full.md

## References

63 references — full list in the complete paper: https://tomesphere.com/paper/PMC12940555/full.md

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Source: https://tomesphere.com/paper/PMC12940555