Anticancer Activity of Plant Tocotrienols, Fucoxanthin, Fucoidan, and Polyphenols in Dietary Supplements
Plants and algae harbor diverse molecules with antioxidant activity and have been demonstrated to directly inhibit cancer cell growth and mitigate the oxidative damage associated with certain antitumor therapies. While antioxidant supplementation, either alone or in combination with chemotherapy, ha...
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creator | Lara-Hernández, Gabriel Ramos-Silva, José Alberto Pérez-Soto, Elvia Figueroa, Mario Flores-Berrios, Ericka Patricia Sánchez-Chapul, Laura Andrade-Cabrera, José Luis Luna-Angulo, Alexandra Landa-Solís, Carlos Avilés-Arnaut, Hamlet |
description | Plants and algae harbor diverse molecules with antioxidant activity and have been demonstrated to directly inhibit cancer cell growth and mitigate the oxidative damage associated with certain antitumor therapies. While antioxidant supplementation, either alone or in combination with chemotherapy, has shown promise in improving quality of life, further research is needed to explore the effects of antioxidant combinations on specific cancer cell lines.
In this study, the in vitro cytotoxic and apoptotic properties of natural compounds derived from plants and algae, as well as certain dietary supplements, were investigated against various human cancer cell lines, including bone, leukemia, colorectal, breast, and prostate cancers.
Apple polyphenols, fucoxanthin, and plant-derived tocotrienols exhibited cytotoxic effects across all lines; however, tocotrienols demonstrated the most potent, time-dependent cytotoxic activity, with a half-inhibitory concentration (IC
) of 4.3 μg/mL in bone cancer cells. Analysis of dietary supplements 2.1, 4.0, and 10.0 revealed that supplement 10.0 exhibited specific cytotoxic activity against bone cancer line TIB-223 and colorectal cancer cell line Caco2, with IC
values of 126 μg/mL and 158 μg/mL, respectively. Both tocotrienols and supplement 10.0 induced morphological changes in TIB-223 cells, inhibited cell migration (anti-metastatic activity), and promoted apoptosis, as evidenced by caspase 3/7 activation in both bone and colorectal cancer cells.
These findings provide valuable insights for the development of targeted dietary supplements to enhance the anticancer effect of conventional chemotherapy in specific cancer types. |
doi_str_mv | 10.3390/nu16244274 |
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In this study, the in vitro cytotoxic and apoptotic properties of natural compounds derived from plants and algae, as well as certain dietary supplements, were investigated against various human cancer cell lines, including bone, leukemia, colorectal, breast, and prostate cancers.
Apple polyphenols, fucoxanthin, and plant-derived tocotrienols exhibited cytotoxic effects across all lines; however, tocotrienols demonstrated the most potent, time-dependent cytotoxic activity, with a half-inhibitory concentration (IC
) of 4.3 μg/mL in bone cancer cells. Analysis of dietary supplements 2.1, 4.0, and 10.0 revealed that supplement 10.0 exhibited specific cytotoxic activity against bone cancer line TIB-223 and colorectal cancer cell line Caco2, with IC
values of 126 μg/mL and 158 μg/mL, respectively. Both tocotrienols and supplement 10.0 induced morphological changes in TIB-223 cells, inhibited cell migration (anti-metastatic activity), and promoted apoptosis, as evidenced by caspase 3/7 activation in both bone and colorectal cancer cells.
These findings provide valuable insights for the development of targeted dietary supplements to enhance the anticancer effect of conventional chemotherapy in specific cancer types.</description><identifier>ISSN: 2072-6643</identifier><identifier>EISSN: 2072-6643</identifier><identifier>DOI: 10.3390/nu16244274</identifier><identifier>PMID: 39770896</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Algae ; Antineoplastic Agents - pharmacology ; Antioxidants ; Antioxidants - pharmacology ; Apoptosis ; Apoptosis - drug effects ; Bone cancer ; Breast cancer ; Caco-2 Cells ; Cancer ; Cancer therapies ; Cell Line, Tumor ; Chemotherapy ; Colorectal cancer ; Cytotoxicity ; Dietary Supplements ; Gas flow ; Humans ; Leukemia ; Metastasis ; Morphology ; Mortality ; Plant Extracts - pharmacology ; Polyphenols ; Polyphenols - pharmacology ; Polysaccharides - pharmacology ; Prostate cancer ; Side effects ; Tocotrienols - pharmacology ; Tumors ; Xanthophylls - pharmacology</subject><ispartof>Nutrients, 2024-12, Vol.16 (24), p.4274</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c307t-e9d648595a77ee4ee5ba661861416d1e4ad3c6c59b0513faad949e5bea3e89a53</cites><orcidid>0000-0002-0680-8516 ; 0000-0002-5673-0825 ; 0000-0002-4268-2279 ; 0000-0001-7004-0591</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39770896$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lara-Hernández, Gabriel</creatorcontrib><creatorcontrib>Ramos-Silva, José Alberto</creatorcontrib><creatorcontrib>Pérez-Soto, Elvia</creatorcontrib><creatorcontrib>Figueroa, Mario</creatorcontrib><creatorcontrib>Flores-Berrios, Ericka Patricia</creatorcontrib><creatorcontrib>Sánchez-Chapul, Laura</creatorcontrib><creatorcontrib>Andrade-Cabrera, José Luis</creatorcontrib><creatorcontrib>Luna-Angulo, Alexandra</creatorcontrib><creatorcontrib>Landa-Solís, Carlos</creatorcontrib><creatorcontrib>Avilés-Arnaut, Hamlet</creatorcontrib><title>Anticancer Activity of Plant Tocotrienols, Fucoxanthin, Fucoidan, and Polyphenols in Dietary Supplements</title><title>Nutrients</title><addtitle>Nutrients</addtitle><description>Plants and algae harbor diverse molecules with antioxidant activity and have been demonstrated to directly inhibit cancer cell growth and mitigate the oxidative damage associated with certain antitumor therapies. While antioxidant supplementation, either alone or in combination with chemotherapy, has shown promise in improving quality of life, further research is needed to explore the effects of antioxidant combinations on specific cancer cell lines.
In this study, the in vitro cytotoxic and apoptotic properties of natural compounds derived from plants and algae, as well as certain dietary supplements, were investigated against various human cancer cell lines, including bone, leukemia, colorectal, breast, and prostate cancers.
Apple polyphenols, fucoxanthin, and plant-derived tocotrienols exhibited cytotoxic effects across all lines; however, tocotrienols demonstrated the most potent, time-dependent cytotoxic activity, with a half-inhibitory concentration (IC
) of 4.3 μg/mL in bone cancer cells. Analysis of dietary supplements 2.1, 4.0, and 10.0 revealed that supplement 10.0 exhibited specific cytotoxic activity against bone cancer line TIB-223 and colorectal cancer cell line Caco2, with IC
values of 126 μg/mL and 158 μg/mL, respectively. Both tocotrienols and supplement 10.0 induced morphological changes in TIB-223 cells, inhibited cell migration (anti-metastatic activity), and promoted apoptosis, as evidenced by caspase 3/7 activation in both bone and colorectal cancer cells.
These findings provide valuable insights for the development of targeted dietary supplements to enhance the anticancer effect of conventional chemotherapy in specific cancer types.</description><subject>Algae</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antioxidants</subject><subject>Antioxidants - pharmacology</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Bone cancer</subject><subject>Breast cancer</subject><subject>Caco-2 Cells</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Cell Line, Tumor</subject><subject>Chemotherapy</subject><subject>Colorectal cancer</subject><subject>Cytotoxicity</subject><subject>Dietary Supplements</subject><subject>Gas flow</subject><subject>Humans</subject><subject>Leukemia</subject><subject>Metastasis</subject><subject>Morphology</subject><subject>Mortality</subject><subject>Plant Extracts - pharmacology</subject><subject>Polyphenols</subject><subject>Polyphenols - pharmacology</subject><subject>Polysaccharides - pharmacology</subject><subject>Prostate cancer</subject><subject>Side effects</subject><subject>Tocotrienols - pharmacology</subject><subject>Tumors</subject><subject>Xanthophylls - pharmacology</subject><issn>2072-6643</issn><issn>2072-6643</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNptkU1PxCAQhonRqFEv_gBD4sUYV6FQKMfN-pmYaKKeG5ZOXUwLtVDj_ntZ1-8IB4bJM8PwvgjtUnLMmCInbqAi4zyTfAVtZkRmIyE4W_0Rb6CdEJ7IYkkiBVtHG0xJSQolNtFs7KI12hno8dhE-2LjHPsa3zbaRXzvjY-9BeebcITPB-NfU3pm3fJiK50i7Sp865t5N3vnsHX41ELU_RzfDV3XQAsuhm20VusmwM7HuYUezs_uJ5ej65uLq8n4emQYkXEEqhK8yFWupQTgAPlUC0ELQTkVFQWuK2aEydWU5JTVWleKqwSBZlAonbMtdLDs2_X-eYAQy9YGA036D_ghlIzmrJCEEZbQ_T_okx96l6ZLFFcyowUvvqlH3UBpXZ0U0WbRtBwXGVVJfrF49vgfKu0KWmu8g9qm_K-Cw2WB6X0IPdRl19s2iVZSUi6cLb-dTfDex6TDtIXqC_30kb0BVLicag</recordid><startdate>20241211</startdate><enddate>20241211</enddate><creator>Lara-Hernández, Gabriel</creator><creator>Ramos-Silva, José Alberto</creator><creator>Pérez-Soto, Elvia</creator><creator>Figueroa, Mario</creator><creator>Flores-Berrios, Ericka Patricia</creator><creator>Sánchez-Chapul, Laura</creator><creator>Andrade-Cabrera, José Luis</creator><creator>Luna-Angulo, Alexandra</creator><creator>Landa-Solís, Carlos</creator><creator>Avilés-Arnaut, Hamlet</creator><general>MDPI AG</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0680-8516</orcidid><orcidid>https://orcid.org/0000-0002-5673-0825</orcidid><orcidid>https://orcid.org/0000-0002-4268-2279</orcidid><orcidid>https://orcid.org/0000-0001-7004-0591</orcidid></search><sort><creationdate>20241211</creationdate><title>Anticancer Activity of Plant Tocotrienols, Fucoxanthin, Fucoidan, and Polyphenols in Dietary Supplements</title><author>Lara-Hernández, Gabriel ; 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While antioxidant supplementation, either alone or in combination with chemotherapy, has shown promise in improving quality of life, further research is needed to explore the effects of antioxidant combinations on specific cancer cell lines.
In this study, the in vitro cytotoxic and apoptotic properties of natural compounds derived from plants and algae, as well as certain dietary supplements, were investigated against various human cancer cell lines, including bone, leukemia, colorectal, breast, and prostate cancers.
Apple polyphenols, fucoxanthin, and plant-derived tocotrienols exhibited cytotoxic effects across all lines; however, tocotrienols demonstrated the most potent, time-dependent cytotoxic activity, with a half-inhibitory concentration (IC
) of 4.3 μg/mL in bone cancer cells. Analysis of dietary supplements 2.1, 4.0, and 10.0 revealed that supplement 10.0 exhibited specific cytotoxic activity against bone cancer line TIB-223 and colorectal cancer cell line Caco2, with IC
values of 126 μg/mL and 158 μg/mL, respectively. Both tocotrienols and supplement 10.0 induced morphological changes in TIB-223 cells, inhibited cell migration (anti-metastatic activity), and promoted apoptosis, as evidenced by caspase 3/7 activation in both bone and colorectal cancer cells.
These findings provide valuable insights for the development of targeted dietary supplements to enhance the anticancer effect of conventional chemotherapy in specific cancer types.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>39770896</pmid><doi>10.3390/nu16244274</doi><orcidid>https://orcid.org/0000-0002-0680-8516</orcidid><orcidid>https://orcid.org/0000-0002-5673-0825</orcidid><orcidid>https://orcid.org/0000-0002-4268-2279</orcidid><orcidid>https://orcid.org/0000-0001-7004-0591</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Algae Antineoplastic Agents - pharmacology Antioxidants Antioxidants - pharmacology Apoptosis Apoptosis - drug effects Bone cancer Breast cancer Caco-2 Cells Cancer Cancer therapies Cell Line, Tumor Chemotherapy Colorectal cancer Cytotoxicity Dietary Supplements Gas flow Humans Leukemia Metastasis Morphology Mortality Plant Extracts - pharmacology Polyphenols Polyphenols - pharmacology Polysaccharides - pharmacology Prostate cancer Side effects Tocotrienols - pharmacology Tumors Xanthophylls - pharmacology |
title | Anticancer Activity of Plant Tocotrienols, Fucoxanthin, Fucoidan, and Polyphenols in Dietary Supplements |
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