| Literature DB >> 35323507 |
Ishtiaq Ahmed1,2, Muhammad Asgher3, Farooq Sher4, Syed Makhdoom Hussain5, Nadia Nazish6, Navneet Joshi7, Ashutosh Sharma8, Roberto Parra-Saldívar9, Muhammad Bilal10, Hafiz M N Iqbal9.
Abstract
This review highlights the underexplored potential and promises of marine bioactive peptides (MBPs) with unique structural, physicochemical, and biological activities to fight against the current and future human pathologies. A particular focus is given to the marine environment as a significant source to obtain or extract high-value MBPs from touched/untouched sources. For instance, marine microorganisms, including microalgae, bacteria, fungi, and marine polysaccharides, are considered prolific sources of amino acids at large, and peptides/polypeptides in particular, with fundamental structural sequence and functional entities of a carboxyl group, amine, hydrogen, and a variety of R groups. Thus, MBPs with tunable features, both structural and functional entities, along with bioactive traits of clinical and therapeutic value, are of ultimate interest to reinforce biomedical settings in the 21st century. On the other front, as the largest biome globally, the marine biome is the so-called "epitome of untouched or underexploited natural resources" and a considerable source with significant potentialities. Therefore, considering their biological and biomedical importance, researchers around the globe are redirecting and/or regaining their interests in valorizing the marine biome-based MBPs. This review focuses on the widespread bioactivities of MBPs, FDA-approved MBPs in the market, sustainable development goals (SDGs), and legislation to valorize marine biome to underlying the impact role of bioactive elements with the related pathways. Finally, a detailed overview of current challenges, conclusions, and future perspectives is also given to satisfy the stimulating demands of the pharmaceutical sector of the modern world.Entities:
Keywords: bioactivities; biomedical; marine bioactive peptides; marine biome; natural resources; pharmacology; therapeutic attributes
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Year: 2022 PMID: 35323507 PMCID: PMC8948685 DOI: 10.3390/md20030208
Source DB: PubMed Journal: Mar Drugs ISSN: 1660-3397 Impact factor: 5.118
Figure 1The literature screening results attained from the Scopus database. The letters A–C characterize the search terms: (A) bioactive compounds from marine sources; (B) bioactive peptides from marine sources; (C) biomedical applications of marine peptides. The letters [a1]–[c1] correspond to the number of articles from all years in that specific category of search term, [b2]–[c2] represents the number of articles published in different journals, and [a3]–[c3] represents the number of articles based on territory. Data were extracted from https://www.scopus.com, access on 25 April 2021.
The literature screening results attained from the PubMed database. Data were extracted from https://pubmed.ncbi.nlm.nih.gov/, access on 25 April 2021.
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| Bioactive compounds from marine sources | 995 | 74 | 172 | 147 | 97 | 101 | 404 |
| Bioactive peptides from marine sources | 307 | 15 | 41 | 52 | 36 | 34 | 129 |
| Biomedical applications of marine peptides | 76 | 3 | 10 | 15 | 11 | 6 | 31 |
Figure 2Various marine sources, along with their representative products or byproducts that have been either accepted or granted to enter the clinical trials.
Marine-based peptides (MBPs) with different bioactivities and applications.
| Peptide Name | Structure | Chemical Formula | Molar Mass (g/mol) | Class or Type of Chemical Compounds | Bioactivities and/or Proposed Applications | References |
|---|---|---|---|---|---|---|
| Astaxanthin |
| C40H52O4 | 596.84 | Terpenes | Nutraceutical and pharmaceutical applications | Messina et al. [ |
| Cyclopolypeptide, e.g., α-amanitin, rolloamide A |
| C39H54N10O14S | 918.97 | Cyclic octopeptide | Antibacterial activity, antifungal activity, anthelmintic activity | Dahiya et al. [ |
| Plitidepsin |
| C57H87N7O15 | 1110.357 | Cyclic depsipeptide | Effective against various cancers, e.g., breast, thyroid, lung, etc. | Leisch et al. [ |
| Borophycin |
| C44H68BO14 | 831.8 | Organic compounds | Various carcinoma types, e.g., epidermoid and human colorectal adenocarcinoma | Nowruzi et al. [ |
| Cryptophycin-52 |
| C35H43ClN2O8 | 655.2 | Depsipeptide | Tumor cell lines | Nowruzi et al. [ |
| Fucoxanthin |
| C42H58O6 | 658.920 | Carotenoids | Gastric cancer | Zhu et al. [ |
| Pardaxin | _ | C154H248N36O45 | 3323.8 | Cationic peptide | Oral squamous cell carcinoma | Han et al. [ |
| Hepcidin | _ | C113H170N34O31S9 | 2789.4 | Cationic amphipathic peptide | Human cervical carcinoma, hepatocellular carcinoma, breast adenocarcinoma cell line | Hassana et al. [ |
| Hemiasterlin | _ | C30H46N4O4 | 526.7 | Peptide | Inhibitory effect on microtubule assembly, cell cycle arrest, Apoptosis induction | Lai et al. [ |
| Aurilide |
| C44H75N5O10 | 834.1 | Depsipeptides | Human lung tumor, leukemia, renal, and prostate cancer cell lines | Sato et al. [ |
| Desmethoxymajusculamide C |
| C49H78N8O11 | 955.2 | Cyclic depsipeptide | Human colon HCT-116 | Simmons et al. [ |
| Diazonamide A |
| C40H34CI2N6O6 | 765.6 | Oxazoles | Human tumor cells | Lachia and Moody [ |
| PG155 | _ | _ | 15,500 | Polypeptide | Potent antiangiogenic activity | Zheng et al. [ |
| C-phycocyanin (e.g., Phycocyanobilin) |
| C33H38N4O6 | 586.7 | Phycobiliprotein | Apoptosis induction | Li et al. [ |
| Kahalalide F | _ | C75H124N14O16 | 1477.9 | Depsipeptide | Ovaries, breast, prostate, colon, and liver tumor cells | Sewell et al. [ |
| Vitilevuamide |
| C77H114N14O21S | 1603.9 | Cyclic peptide | Lymphocytic inhibition of tubulin polymerization | Edler et al. [ |
| Tachyplesin |
| C99H151N35O19S4 | 2263.8 | Cationic Peptides | Prostate, Melanoma, and endothelial cancer cell | Chen et al. [ |
| Thiocoraline |
| C48H56N10O12S6 | 1157.4 | Depsipeptides | Human colon cancer | Erba et al. [ |
Figure 3Anticancer potentialities of MBPs to abolish cancer cells and avoid metastasis via apoptosis mechanism. Created with BioRender.com and extracted under premium membership.
Selected FDA-approved MBPs.
| Compound Name | Formula | Molar Mass | CAS Number | Source | Natural/Derivative | Legal Status | Bioavailability 1 | Elimination Half-Life | Applications |
|---|---|---|---|---|---|---|---|---|---|
| Ziconotide (intrathecal ziconotide) | C102H172N36O32S7 | 2639.14 (g/mol) | 107452-89-1 | Cone Snail | Natural product | Prescription only | 50% | 2.9 to 6.5 h | Analgesics |
| Adcetris (Brentuximab vedotin) | C6476H9930N1690O2030S40 | 149.2–151.8 (kg/mol) | 914088-09-8 |
| Derivative | Prescription only | 50–80% | Approximately 4 to 6 days | Cancer treatment, treatment for patients with cutaneous T-cell lymphoma |
| Dactinomycin | C62H86N12O16 | 1255.438 (g/mol) | 50-76-0 |
| Derivative | Prescription only | Not Available | 36 h | Cancer treatment including for Gestational trophoblastic neoplasia, Wilms’ tumor, Rhabdomyosarcoma, Ewing’s sarcoma |
| Bacitracin (Baciim) | C66H103N17O16S | 1422.71 (g/mol) | 1405-87-4 |
| Natural product | Prescription-only for injection and OTC | Not Available | Not Available | Acute and chronic localized skin infections |
| Dutasteride (Avodart) | C27H30F6N2O2 | 528.539 (g/mol) | 164656-23-9 | _ | Synthetic | Prescription-only | 60% | 4–5 Weeks | Treat enlarged prostate, Prostate cancer, hormone therapy |
| Curacin A | C23H35NOS | 373.60 (g/mol) | 155233-30-0 |
| Natural product | Not Available | Not Available | Not Available | Cancer treatment |
| Eribulin (Halaven) | C40H59NO11 | 729.908 (g/mol) | 253128-41-5 | Marine Sponge | _ | Prescription-only | Not Available | 40 h | Cancer treatment |
| Trabectedin (Yondelis) | C39H43N3O11S | 761.84 (g/mol) | 114899-77-3 | Marine Tunicate | Prescription-only | Not Available | 180 h | Antitumor chemotherapy medication for the treatment of advanced soft-tissue sarcoma and ovarian cancer |
1: In pharmacology, bioavailability refers to absorption and is the fraction (%) of an administered drug that reaches the systemic circulation.