OKADAIC ACID IN EUKARYOTIC CELLS: MECHANISMS, IMPACTS ON HUMAN HEALTH, AND CHALLENGES FOR MONITORING
Abstract
Harmful algal blooms (HABs) are characterized by the proliferation of microalgae capable of generating severe impacts on aquatic ecosystems and human health, especially through the consumption of contaminated filter-feeding organisms. Okadaic acid (OA) is one of the main marine toxins associated with these events, being the causative agent of Diarrhetic Shellfish Poisoning (DSP). Currently, there is growing evidence of its toxic effects across various biological models. This review article analyzes the literature published between 2019 and 2025 to elucidate the most recent evidence regarding OA toxicity. The study focuses on its mechanisms of action, clinical manifestations, chronic and ecotoxicological effects, in addition to evaluating current detection methods and risk management strategies. Finally, the review highlights knowledge gaps and recommends priorities for research and surveillance, aiming to mitigate risks to public health and aquaculture.
Author Biographies
Master's student in Environmental Engineering at the Instituto Federal Fluminense (IFF).
Ph.D. student in Modeling and Technology for Environment Applied to Water Resources at IFF. Professor at the Municipality of Araruama.
Ph.D. in Experimental Clinical Pathophysiology from the Rio de Janeiro State University (UERJ). Professor in the Graduate Program in Plant Biology at UERJ.
Ph.D. in Experimental Clinical Pathophysiology from the Rio de Janeiro State University (UERJ). Professor in the Graduate Program in Plant Biology at UERJ.
Ph.D. in Human Rights from the University of Coimbra. Professor in the Graduate Program in Environmental Engineering at IFF.
Ph.D. in Biological Sciences (Biophysics) from UERJ. Professor of Biology at IFF.
Ph.D. in Biological Sciences (Nuclear Biosciences) from UERJ. Professor in the Graduate Program in Plant Biology at UERJ.
Ph.D. in Biological Sciences (Nuclear Biosciences) from UERJ. Professor in the Graduate Program in Environmental Engineering at IFF.
References
Alarcan, J., Barbé, S., Kopp, B., Hessel-Pras, S., Braeuning, A., Lampen, A., Le Hégarat, L., & Fessard, V. (2019). Combined effects of okadaic acid and pectenotoxin-2, 13-desmethylspirolide C or yessotoxin in human intestinal Caco-2 cells. Chemosphere, 228, 139–148. https://doi.org/10.1016/j.chemosphere.2019.04.018 DOI: https://doi.org/10.1016/j.chemosphere.2019.04.018
Almeida, E. A., Bainy, A. C. D., Loureiro, A. P. M., Martinez, G. R., Miyamoto, S., Onuki, J., Barbosa, L. F., Garcia, C. C. M., Prado, F. M., Ronsein, G. E., Sigolo, C. A., Brochini, C. B., Martins, A. M. G., Medeiros, M. H. G., & Di Mascio, P. (2007). Oxidative stress in Perna perna and other bivalves as indicators of environmental stress in the Brazilian marine environment: Antioxidants, lipid peroxidation and DNA damage. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 146(4), 588–600. https://doi.org/10.1016/j.cbpa.2006.02.040 DOI: https://doi.org/10.1016/j.cbpa.2006.02.040
Bacchiocchi, S., Siracusa, M., Barchiesi, F., Maresca, C., Ferroni, L., Calandri, E., Tavoloni, T., Giuliani, M. E., Accoroni, S., Stramenga, A., & Piersanti, A. (2025). Long term study (2012−2021) on okadaic acid and yessotoxins in Northwestern Adriatic Sea mussels (Italy): The role of inland rainfall in the dynamics of contamination events. Marine Pollution Bulletin, 221, 118558. https://doi.org/10.1016/j.marpolbul.2025.118558 DOI: https://doi.org/10.1016/j.marpolbul.2025.118558
Bian, Y., Feng, X. S., Zhang, Y., Du, C., & Wen, Y. Q. (2024). Marine toxins in environment: Recent updates on depuration techniques. Ecotoxicology and Environmental Safety, 284, 116990. https://doi.org/10.1016/j.ecoenv.2024.116990 DOI: https://doi.org/10.1016/j.ecoenv.2024.116990
Camacho-Muñoz, D., Lawton, L. A., & Edwards, C. (2020). Degradation of okadaic acid in seawater by UV/TiO2 photocatalysis – Proof of concept. Science of The Total Environment, 733, 139346. https://doi.org/10.1016/j.scitotenv.2020.139346 DOI: https://doi.org/10.1016/j.scitotenv.2020.139346
Carvalho Pinto-Silva, C. R., Ferreira, J. F., Costa, R. H. R., Belli Filho, P., Creppy, E. E., & Matias, W. G. (2003). Micronucleus induction in mussels exposed to okadaic acid. Toxicon, 41(1), 93–97. https://doi.org/10.1016/s0041-0101(02)00214-3 DOI: https://doi.org/10.1016/S0041-0101(02)00214-3
Cavion, F., Sosa, S., Kilcoyne, J., D'Arelli, A., Ponti, C., Carlin, M., Tubaro, A., & Pelin, M. (2025). Effects of dinoflagellate toxins okadaic acid and dinophysistoxin-1 and -2 on the microcrustacean Artemia franciscana. Toxins, 17(2), 80. https://doi.org/10.3390/toxins17020080 DOI: https://doi.org/10.3390/toxins17020080
Chen, Y. M., Lee, T. H., Lee, S. J., Huang, H. B., Huang, R., & Chou, H. N. (2006). Comparison of protein phosphatase inhibition activities and mouse toxicities of microcystins. Toxicon, 47(7), 742–746. https://doi.org/10.1016/j.toxicon.2006.01.026 DOI: https://doi.org/10.1016/j.toxicon.2006.01.026
Corriere, M., Soliño, L., & Costa, P. R. (2021). Effects of the marine biotoxins okadaic acid and dinophysistoxins on fish. Journal of Marine Science and Engineering, 9(3), 293. https://doi.org/10.3390/jmse9030293 DOI: https://doi.org/10.3390/jmse9030293
Cristóbal, I., Manso, R., Rincón, R., Caramés, C., Senin, C., Borrero, A., Martínez-Useros, J., Rodriguez, M., Zazo, S., Aguilera, O., Madoz-Gúrpide, J., Rojo, F., & García-Foncillas, J. (2014). PP2A inhibition is a common event in colorectal cancer and its restoration using FTY720 shows promising therapeutic potential. Molecular Cancer Therapeutics, 13(4), 938–947. https://doi.org/10.1158/1535-7163.MCT-13-0150 DOI: https://doi.org/10.1158/1535-7163.MCT-13-0150
Devillier, V. M., Hall, E. R., Lovko, V., Pierce, R., Anderson, D. M., & Lewis, K. A. (2024). Mesocosm study of PAC-modified clay effects on Karenia brevis cells and toxins, chemical dynamics, and benthic invertebrate physiology. Harmful Algae, 134, 102609. https://doi.org/10.1016/j.hal.2024.102609 DOI: https://doi.org/10.1016/j.hal.2024.102609
European Food Safety Authority. (2021). Evaluation of the shucking of certain species of scallops contaminated with lipophilic toxins with a view to the production of edible parts meeting the safety requirements foreseen in the Union legislation. EFSA Journal, 19(3), Artigo e06422. https://doi.org/10.2903/j.efsa.2021.6422 DOI: https://doi.org/10.2903/j.efsa.2021.6422
Flórez-Barrós, F., Prado-Alvarez, M., Méndez, J., & Fernández-Tajes, J. (2011). Evaluation of genotoxicity in gills and hemolymph of clam Ruditapes decussatus fed with the toxic dinoflagellate Prorocentrum lima. Journal of Toxicology and Environmental Health, Part A, 74(15-16), 971–979. https://doi.org/10.1080/15287394.2011.582025 DOI: https://doi.org/10.1080/15287394.2011.582025
Food and Agriculture Organization of the United Nations. (2025). Fishery and aquaculture statistics: Yearbook 2023. https://doi.org/10.4060/cd6788en DOI: https://doi.org/10.4060/cd6788en
Fu, L. L., Zhao, X. Y., Ji, L. D., & Xu, J. (2019). Okadaic acid (OA): Toxicity, detection and detoxification. Toxicon, 160, 1–7. https://doi.org/10.1016/j.toxicon.2018.12.007 DOI: https://doi.org/10.1016/j.toxicon.2018.12.007
Fujiki, H., & Suganuma, M. (1993). Tumor promotion by inhibitors of protein phosphatases 1 and 2A: The okadaic acid class of compounds. In G. F. Vande Woude & G. Klein (Eds.), Advances in cancer research (Vol. 61, pp. 143–194). Academic Press. https://doi.org/10.1016/S0065-230X(08)60307-0 DOI: https://doi.org/10.1016/S0065-230X(08)60958-6
Fujiki, H., Suganuma, M., Okabe, S., Sueoka, E., Suga, K., Imai, K., & Nakachi, K. (2000). A new concept of tumor promotion by tumor necrosis factor-alpha, and cancer preventive agents (-)-epigallocatechin gallate and green tea—a review. Cancer Detection and Prevention, 24(1), 91–99. https://pubmed.ncbi.nlm.nih.gov/10757128/
Fujiki, H., Sueoka, E., Watanabe, T., & Suganuma, M. (2018). The concept of the okadaic acid class of tumor promoters is revived in endogenous protein inhibitors of protein phosphatase 2A, SET and CIP2A, in human cancers. Journal of Cancer Research and Clinical Oncology, 144(12), 2339–2349. https://doi.org/10.1007/s00432-018-2765-7 DOI: https://doi.org/10.1007/s00432-018-2765-7
Fujiki, H., Sueoka, E., Watanabe, T., Komori, A., & Suganuma, M. (2023). Cancer progression by the okadaic acid class of tumor promoters and endogenous protein inhibitors of PP2A, SET and CIP2A. Journal of Cancer Research and Clinical Oncology, 149(11), 9425–9433. https://doi.org/10.1007/s00432-023-04800-4 DOI: https://doi.org/10.1007/s00432-023-04800-4
Hao, X., Zhang, H., & Lian, Z. (2024). Sensitive detection of okadaic acid in marine sediment using magnetic imprinted fluorescent nanoprobe. Microchemical Journal, 207, 111952. https://doi.org/10.1016/j.microc.2024.111952 DOI: https://doi.org/10.1016/j.microc.2024.111952
Huang, H. J., Liu, Y., Li, D. W., Wang, X., Feng, N. X., Li, H. Y., Mo, C. H., & Yang, W. D. (2025). Polystyrene microplastics can aggravate the damage of the intestinal microenvironment caused by okadaic acid: A prevalent algal toxin. Marine Drugs, 23(3), 129. https://doi.org/10.3390/md23030129 DOI: https://doi.org/10.3390/md23030129
Huang, L., Gong, J., Hu, Y., Tan, Q.-L., Liu, B., Yu, X.-W., Hao, X.-L., & Guo, Q.-N. (2022). Long-term exposure to low levels of okadaic acid accelerates cell cycle progression in colonic epithelial cells via p53 and Jak/Stat3 signaling pathways. Heliyon, 8(9), e10444. https://doi.org/10.1016/j.heliyon.2022.e10444 DOI: https://doi.org/10.1016/j.heliyon.2022.e10444
Huhn, J., Jeffrey, P. D., Larsen, K., Rundberget, T., Rise, F., Cox, N. R., Arcus, V., Shi, Y., & Miles, C. O. (2009). A structural basis for the reduced toxicity of dinophysistoxin-2. Chemical Research in Toxicology, 22(11), 1782–1786. https://doi.org/10.1021/tx900259b DOI: https://doi.org/10.1021/tx9001622
Ikehara, T., & Oshiro, N. (2024). A protein phosphatase 2A-based assay to detect okadaic acids and microcystins. Journal of Marine Science and Engineering, 12(2), 244. https://doi.org/10.3390/jmse12020244 DOI: https://doi.org/10.3390/jmse12020244
Jiménez-Cárcamo, D., García, C., & Contreras, H. R. (2020). Toxins of okadaic acid-group increase malignant properties in cells of colon cancer. Toxins, 12(3), 179. https://doi.org/10.3390/toxins12030179 DOI: https://doi.org/10.3390/toxins12030179
Lenzen, M., Li, M., & Murray, S. A. (2021). Impacts of harmful algal blooms on marine aquaculture in a low-carbon future. Harmful Algae, 110, 102143. https://doi.org/10.1016/j.hal.2021.102143 DOI: https://doi.org/10.1016/j.hal.2021.102143
Lin, P., Lu, Z., Zhang, Y., Ren, L., Sun, S., & Li, C. (2021). Do polystyrene nanoplastics aggravate the toxicity of single contaminants (okadaic acid)? Using AGS cells as a biological model. Environmental Science: Nano, 8(11), 3186–3201. https://doi.org/10.1039/d1en00688f DOI: https://doi.org/10.1039/D1EN00688F
Liu, Y., Yuan, T.-Q., Zheng, J.-W., Li, D.-W., Jiao, Y.-H., Li, H.-Y., Li, R.-M., & Yang, W.-D. (2023). Exposure to okadaic acid could disrupt the colonic microenvironment in rats. Ecotoxicology and Environmental Safety, 263, 115376. https://doi.org/10.1016/j.ecoenv.2023.115376 DOI: https://doi.org/10.1016/j.ecoenv.2023.115376
Louzao, M. C., Abal, P., Costas, C., Suzuki, T., Watanabe, R., Vilariño, N., Botana, A. M., Vieytes, M. R., & Botana, L. M. (2021). DSP toxin distribution across organs in mice after acute oral administration. Marine Drugs, 19(1), 23. https://doi.org/10.3390/md19010023 DOI: https://doi.org/10.3390/md19010023
Lushchak, V. I. (2011). Environmentally induced oxidative stress in aquatic animals. Aquatic Toxicology, 101(1), 13–30. https://doi.org/10.1016/j.aquatox.2010.10.006 DOI: https://doi.org/10.1016/j.aquatox.2010.10.006
Mafra, L. L., Jr., Nolli, P. K. W., Mota, L. E., Domit, C., Soeth, M., Luz, L. F. G., Sobrinho, B. F., Leal, J. G., & Di Domenico, M. (2019). Multi-species okadaic acid contamination and human poisoning during a massive bloom of Dinophysis acuminata complex in southern Brazil. Harmful Algae, 89, 101662. https://doi.org/10.1016/j.hal.2019.101662 DOI: https://doi.org/10.1016/j.hal.2019.101662
Ministry of Agriculture and Livestock of Brazil. (2023). Vigilância de contaminantes em moluscos bivalves [Surveillance of contaminants in bivalve mollusks]. MAPA.
Ministry of Health, Labour and Welfare of Japan. (2015). Notification Shokuan-hatsu 0306 Dai 1 Gō: On the handling of bivalves poisoned by paralytic shellfish toxins, etc. https://www.mhlw.go.jp/file/06-Seisakujouhou-11130500-Shokuhinanzenbu/0000078334.pdf
National Shellfish Sanitation Program. (2019). Guide for the control of molluscan shellfish: 2019 revision. U.S. Food and Drug Administration. http://www.fda.gov/Food/GuidanceRegulation/FederalStateFoodPrograms/ucm2006754.htm
Neves, R. A. F., Chaverra, A., Wieters, E., Foggo, A., & Knights, A. M. (2019). Impacts of the toxic benthic dinoflagellate Prorocentrum lima on the brown mussel Perna perna: Shell-valve closure response, immunology, and histopathology. Marine Environmental Research, 146, 35–45. https://doi.org/10.1016/j.marenvres.2019.03.003 DOI: https://doi.org/10.1016/j.marenvres.2019.03.006
Pal, M., Yesankar, P. J., Dwivedi, A., & Qureshi, A. (2020). Biotic control of harmful algal blooms (HABs): A brief review. Journal of Environmental Management, 268, 110687. https://doi.org/10.1016/j.jenvman.2020.110687 DOI: https://doi.org/10.1016/j.jenvman.2020.110687
Pinto-Silva, C. R. C., Creppy, E. E., & Matias, W. G. (2005). Micronucleus test in mussels Perna perna fed with the toxic dinoflagellate Prorocentrum lima. Archives of Toxicology, 79(7), 422–426. https://doi.org/10.1007/s00204-004-0648-5 DOI: https://doi.org/10.1007/s00204-004-0645-1
Pitt, S. J., & Gunn, A. (2024). The One Health concept. British Journal of Biomedical Science, 81, 12366. https://doi.org/10.3389/bjbs.2024.12366 DOI: https://doi.org/10.3389/bjbs.2024.12366
Pradhan, B., Kim, H., Abassi, S., & Ki, J. S. (2022). Toxic effects and tumor promotion activity of marine phytoplankton toxins: A review. Toxins, 14(6), 397. https://doi.org/10.3390/toxins14060397 DOI: https://doi.org/10.3390/toxins14060397
Prego-Faraldo, M. V., Vieira, L. R., Eirin-Lopez, J. M., Méndez, J., & Guilhermino, L. (2017). Transcriptional and biochemical analysis of antioxidant enzymes in the mussel Mytilus galloprovincialis during experimental exposures to the toxic dinoflagellate Prorocentrum lima. Marine Environmental Research, 129, 304–315. https://doi.org/10.1016/j.marenvres.2017.06.012 DOI: https://doi.org/10.1016/j.marenvres.2017.06.009
Qin, Y., Li, J., Song, S., Jiang, J., Kong, J., Zhang, Z., Zhang, C., Zheng, X., Han, B., & Han, B. N. (2022). Sensitive time-resolved fluoroimmunoassay for the quantitative detection of okadaic acid. Frontiers in Marine Science, 9, 893820. https://doi.org/10.3389/fmars.2022.893820 DOI: https://doi.org/10.3389/fmars.2022.961751
Qin, Y., Li, J., Song, S., Jiang, J., Kong, J., Zhang, Z., Zhang, C., Zheng, X., Han, B., & Han, B. N. (2023). Okadaic acid detection through a rapid and sensitive amplified luminescent proximity homogeneous assay. Toxins, 15(8), 501. https://doi.org/10.3390/toxins15080501 DOI: https://doi.org/10.3390/toxins15080501
Roberts, V. A., Vigar, M., Backer, L., Veytsel, G. E., Hilborn, E. D., Hamelin, E. I., Vanden Esschert, K. L., Lively, J. Y., Cope, J. R., Hlavsa, M. C., & Yoder, J. S. (2020). Surveillance for harmful algal bloom events and associated human and animal illnesses — One Health Harmful Algal Bloom System, United States, 2016–2018. Morbidity and Mortality Weekly Report, 69(50), 1889–1894. https://doi.org/10.15585/mmwr.mm6950a2 DOI: https://doi.org/10.15585/mmwr.mm6950a2
Rodríguez-Santos, L., Blanco, J., Botana, L. M., & Vilariño, N. (2024). Bioavailability profiling shows differences in OA, DTX1 and DTX2 toxins that justify their toxicity. Chemosphere, 366, 143419. https://doi.org/10.1016/j.chemosphere.2024.143419 DOI: https://doi.org/10.1016/j.chemosphere.2024.143419
Soliño, L., & Costa, P. R. (2020). Global impact of ciguatoxins and ciguatera fish poisoning on fish, fisheries and consumers. Environmental Research, 182, 109111. https://doi.org/10.1016/j.envres.2020.109111 DOI: https://doi.org/10.1016/j.envres.2020.109111
Song, H., Wang, J., Xue, S., Zhang, S., Zhang, Y., & Chang, Y. (2024). Short-term exposure to okadaic acid induces behavioral and physiological responses in sea urchin (Strongylocentrotus intermedius). Marine Environmental Research, 202, 106823. https://doi.org/10.1016/j.marenvres.2024.106823 DOI: https://doi.org/10.1016/j.marenvres.2024.106823
Song, M., Yin, Y., Chen, Z., Zhang, L., & Yang, W. (2022). De novo design of DNA aptamers that target okadaic acid (OA) by docking-then-assembling of single nucleotides. Biosensors and Bioelectronics, 215, 114562. https://doi.org/10.1016/j.bios.2022.114562 DOI: https://doi.org/10.1016/j.bios.2022.114562
Suganuma, M., Fujiki, H., Suguri, H., Yoshizawa, S., Hirota, M., Nakayasu, M., Ojika, M., Wakamatsu, K., Yamada, K., & Sugimura, T. (1988). Okadaic acid: An additional non-phorbol-12-tetradecanoate-13-acetate-type tumor promoter. Proceedings of the National Academy of Sciences, 85(6), 1768–1771. https://doi.org/10.1073/pnas.85.6.1768 DOI: https://doi.org/10.1073/pnas.85.6.1768
Suganuma, M., Fujiki, H., Okabe, S., Nishiwaki, S., Brautigan, D., Ingebritsen, T. S., & Rosner, M. R. (1992). Structurally different members of the okadaic acid class selectively inhibit protein serine/threonine but not tyrosine phosphatase activity. Toxicon, 30(8), 873–878. https://doi.org/10.1016/0041-0101(92)90386-s DOI: https://doi.org/10.1016/0041-0101(92)90385-I
Tan, K., Zheng, H., Zhang, H., Sun, Y., & Li, Q. (2023). Effects of harmful algal blooms on the physiological, immunity and resistance to environmental stress of bivalves: Special focus on paralytic shellfish poisoning and diarrhetic shellfish poisoning. Aquaculture, 563, 739000. https://doi.org/10.1016/j.aquaculture.2022.739000 DOI: https://doi.org/10.1016/j.aquaculture.2022.739000
Tian, Y., Wang, Z., Zhang, M., Zhao, S., & Li, P. (2022). Sensitive detection of the okadaic acid marine toxin in shellfish by Au@Pt NPs/horseradish peroxidase dual catalysis immunoassay. Analytical Methods, 14(12), 1261–1267. https://doi.org/10.1039/d2ay00095d DOI: https://doi.org/10.1039/D1AY01973B
Trottet, A., George, C., Shen, Y., Gu, J., & Wang, X. (2022). Aquaculture in coastal urbanized areas: A comparative review of the challenges posed by harmful algal blooms. Critical Reviews in Environmental Science and Technology, 52(16), 2888–2929. https://doi.org/10.1080/10643389.2021.1900764 DOI: https://doi.org/10.1080/10643389.2021.1897372
Turner, A. D., Dhanji-Rapkova, M., Coates, L., Bickerstaff, L., & Lewis, A. M. (2021). Marine invertebrate interactions with harmful algal blooms – Implications for One Health. Journal of Invertebrate Pathology, 186, 107555. https://doi.org/10.1016/j.jip.2021.107555 DOI: https://doi.org/10.1016/j.jip.2021.107555
Valdiglesias, V., Prego-Faraldo, M. V., Pásaro, E., Méndez, J., & Laffon, B. (2010). Assessment of okadaic acid effects on cytotoxicity, DNA damage and DNA repair in human cells. Mutation Research, 689(1), 74–79. https://doi.org/10.1016/j.mrfmmm.2010.05.004 DOI: https://doi.org/10.1016/j.mrfmmm.2010.05.004
Valdiglesias, V., Pásaro, E., Méndez, J., & Laffon, B. (2011a). Induction of oxidative DNA damage by the marine toxin okadaic acid depends on human cell type. Toxicon, 57(6), 882–888. https://doi.org/10.1016/j.toxicon.2011.03.005 DOI: https://doi.org/10.1016/j.toxicon.2011.03.005
Valdiglesias, V., Pásaro, E., Méndez, J., & Laffon, B. (2011b). Okadaic acid induces morphological changes, apoptosis and cell cycle alterations in different human cell types. Journal of Environmental Monitoring, 13(6), 1831–1840. https://doi.org/10.1039/c1em10074h DOI: https://doi.org/10.1039/c0em00771d
Valdiglesias, V., Prego-Faraldo, M. V., Pásaro, E., Méndez, J., & Laffon, B. (2013). Okadaic acid: More than a diarrheic toxin. Marine Drugs, 11(11), 4328–4349. https://doi.org/10.3390/md11114328 DOI: https://doi.org/10.3390/md11114328
Verbinnen, I., Ferreira, M., & Janssens, V. (2021). Protein Phosphatase 2A (PP2A) mutations in brain function, development, and neurologic disease. Biochemical Society Transactions, 49(4), 1567–1588. https://doi.org/10.1042/BST20200707 DOI: https://doi.org/10.1042/BST20201313
Vieira, A., Silva, M., Silva, R., Costa, P. R., & Louzao, M. C. (2013). Oral toxicity of okadaic acid in mice: Study of lethality, organ damage, distribution and effects on detoxifying gene expression. Toxins, 5(11), 2093–2108. https://doi.org/10.3390/toxins5112093 DOI: https://doi.org/10.3390/toxins5112093
Wang, X., Wang, Y., Sun, X., Zhang, Y., & Li, C. (2021). iTRAQ-based quantitative proteomic analysis reveals toxicity mechanisms in Chlamys farreri exposed to okadaic acid. Frontiers in Marine Science, 8, 792050. https://doi.org/10.3389/fmars.2021.792050 DOI: https://doi.org/10.3389/fmars.2021.792050
Wang, Y., Li, Z., Liu, H., Chen, Q., & Zhang, H. (2021). Aptamer-based microcantilever-array biosensor for ultra-sensitive and rapid detection of okadaic acid. Microchemical Journal, 160, 105644. https://doi.org/10.1016/j.microc.2020.105644 DOI: https://doi.org/10.1016/j.microc.2020.105644
Wang, Y., Zhang, X., Yang, W., & Li, H. (2024). Precautions for seafood consumers: An updated review of toxicity, bioaccumulation, and rapid detection methods of marine biotoxins. Ecotoxicology and Environmental Safety, 274, 116201. https://doi.org/10.1016/j.ecoenv.2024.116201 DOI: https://doi.org/10.1016/j.ecoenv.2024.116201
Wells, M. L., Karlson, B., Wulff, A., Kudela, R., Trick, C., Asakawa, V., Mantovani, E., & Davidson, K. (2020). Future HAB science: Directions and challenges in a changing climate. Harmful Algae, 91, 101632. https://doi.org/10.1016/j.hal.2020.101632 DOI: https://doi.org/10.1016/j.hal.2019.101632
Weng, Q., Chen, J., Wu, Y., & Zhao, Y. (2024). Occurrence and exposure assessment of lipophilic shellfish toxins in the Zhejiang Province, China. Marine Drugs, 22(6), 239. https://doi.org/10.3390/md22060239 DOI: https://doi.org/10.3390/md22060239
Wu, H., Zhang, Y., Sun, L., Li, X., & Wang, Q. (2020). Nontarget screening and toxicity evaluation of diol esters of okadaic acid and dinophysistoxins reveal intraspecies difference of Prorocentrum lima. Environmental Science & Technology, 54(19), 12366–12375. https://doi.org/10.1021/acs.est.0c03443 DOI: https://doi.org/10.1021/acs.est.0c03691
Wuerger, L. T. D., Lichtner, M., & Braeuning, A. (2023a). Okadaic acid activates JAK/STAT signaling to affect xenobiotic metabolism in HepaRG cells. Cells, 12(5), 770. https://doi.org/10.3390/cells12050770 DOI: https://doi.org/10.3390/cells12050770
Wuerger, L. T. D., Lichtner, M., & Braeuning, A. (2023b). Proteomic analysis of hepatic effects of okadaic acid in HepaRG human liver cells. EXCLI Journal, 22, 1135–1145. https://doi.org/10.17179/excli2023-6444
Wuerger, L. T. D., Lichtner, M., & Braeuning, A. (2024). A multi-omics approach to elucidate okadaic acid-induced changes in human HepaRG hepatocarcinoma cells. Archives of Toxicology, 98(9), 2919–2935. https://doi.org/10.1007/s00204-024-03762-1 DOI: https://doi.org/10.1007/s00204-024-03796-1
Yang, Y., Liu, X., Wang, Q., Li, J., & Zhang, S. (2023). Effects of lipophilic phycotoxin okadaic acid on the early development and transcriptional expression of marine medaka Oryzias melastigma. Aquatic Toxicology, 260, 106576. https://doi.org/10.1016/j.aquatox.2023.106576 DOI: https://doi.org/10.1016/j.aquatox.2023.106576
Yuan, K. K., Li, H. Y., & Yang, W. D. (2024). Marine algal toxins and public health: Insights from shellfish and fish, the main biological vectors. Marine Drugs, 22(11), 510. https://doi.org/10.3390/md22110510 DOI: https://doi.org/10.3390/md22110510
Zohdi, E., & Abbaspour, M. (2019). Harmful algal blooms (red tide): A review of causes, impacts and approaches to monitoring and prediction. International Journal of Environmental Science and Technology, 16(3), 1789–1806. https://doi.org/10.1007/s13762-018-2108-x DOI: https://doi.org/10.1007/s13762-018-2108-x
