A Brief Overview of the Antitumoral Actions of Leelamine
Identifieur interne : 000B51 ( Main/Exploration ); précédent : 000B50; suivant : 000B52A Brief Overview of the Antitumoral Actions of Leelamine
Auteurs : Myriam Merarchi [France, Singapour] ; Young Yun Jung [Corée du Sud] ; Lu Fan [Singapour] ; Gautam Sethi [Singapour] ; Kwang Seok Ahn [Corée du Sud]Source :
- Biomedicines [ 2227-9059 ] ; 2019.
Abstract
For the last couple of decades, natural products, either applied singly or in conjunction with other cancer therapies including chemotherapy and radiotherapy, have allowed us to combat different types of human cancers through the inhibition of their initiation and progression. The principal sources of these useful compounds are isolated from plants that were described in traditional medicines for their curative potential. Leelamine, derived from the bark of pine trees, was previously reported as having a weak agonistic effect on cannabinoid receptors and limited inhibitory effects on pyruvate dehydrogenase kinases (PDKs). It has been reported to possess a strong lysosomotropic property; this feature enables its assembly inside the acidic compartments within a cell, such as lysosomes, which may eventually hinder endocytosis. In this review, we briefly highlight the varied antineoplastic actions of leelamine that have found implications in pharmacological research, and the numerous intracellular targets affected by this agent that can effectively negate the oncogenic process.
Url:
DOI: 10.3390/biomedicines7030053
PubMed: 31330969
PubMed Central: 6783843
Affiliations:
- Corée du Sud, France, Singapour
- Région capitale de Séoul, Île-de-France
- Paris, Séoul
- Université nationale de Singapour
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Merarchi</name><affiliation wicri:level="3"><nlm:aff id="af1-biomedicines-07-00053">Faculty of Pharmacy, University of Paris Descartes, 75006 Paris, France</nlm:aff><country xml:lang="fr">France</country><wicri:regionArea>Faculty of Pharmacy, University of Paris Descartes, 75006 Paris</wicri:regionArea><placeName><region type="region" nuts="2">Île-de-France</region><settlement type="city">Paris</settlement></placeName></affiliation><affiliation wicri:level="4"><nlm:aff id="af2-biomedicines-07-00053">Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117600, Singapore</nlm:aff><country xml:lang="fr">Singapour</country><wicri:regionArea>Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117600</wicri:regionArea><orgName type="university">Université nationale de Singapour</orgName></affiliation></author><author><name sortKey="Jung, Young Yun" sort="Jung, Young Yun" uniqKey="Jung Y" first="Young Yun" last="Jung">Young Yun Jung</name><affiliation wicri:level="1"><nlm:aff id="af3-biomedicines-07-00053">College of Korean Medicine, Kyung Hee University, 24 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Korea</nlm:aff><country xml:lang="fr">Corée du Sud</country><wicri:regionArea>College of Korean Medicine, Kyung Hee University, 24 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447</wicri:regionArea><placeName><settlement type="city">Séoul</settlement><region type="capital">Région capitale de Séoul</region></placeName></affiliation></author><author><name sortKey="Fan, Lu" sort="Fan, Lu" uniqKey="Fan L" first="Lu" last="Fan">Lu Fan</name><affiliation wicri:level="4"><nlm:aff id="af2-biomedicines-07-00053">Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117600, Singapore</nlm:aff><country xml:lang="fr">Singapour</country><wicri:regionArea>Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117600</wicri:regionArea><orgName type="university">Université nationale de Singapour</orgName></affiliation></author><author><name sortKey="Sethi, Gautam" sort="Sethi, Gautam" uniqKey="Sethi G" first="Gautam" last="Sethi">Gautam Sethi</name><affiliation wicri:level="4"><nlm:aff id="af2-biomedicines-07-00053">Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117600, Singapore</nlm:aff><country xml:lang="fr">Singapour</country><wicri:regionArea>Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117600</wicri:regionArea><orgName type="university">Université nationale de Singapour</orgName></affiliation></author><author><name sortKey="Ahn, Kwang Seok" sort="Ahn, Kwang Seok" uniqKey="Ahn K" first="Kwang Seok" last="Ahn">Kwang Seok Ahn</name><affiliation wicri:level="1"><nlm:aff id="af3-biomedicines-07-00053">College of Korean Medicine, Kyung Hee University, 24 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Korea</nlm:aff><country xml:lang="fr">Corée du Sud</country><wicri:regionArea>College of Korean Medicine, Kyung Hee University, 24 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447</wicri:regionArea><placeName><settlement type="city">Séoul</settlement><region type="capital">Région capitale de Séoul</region></placeName></affiliation></author></analytic><series><title level="j">Biomedicines</title><idno type="eISSN">2227-9059</idno><imprint><date when="2019">2019</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>For the last couple of decades, natural products, either applied singly or in conjunction with other cancer therapies including chemotherapy and radiotherapy, have allowed us to combat different types of human cancers through the inhibition of their initiation and progression. The principal sources of these useful compounds are isolated from plants that were described in traditional medicines for their curative potential. Leelamine, derived from the bark of pine trees, was previously reported as having a weak agonistic effect on cannabinoid receptors and limited inhibitory effects on pyruvate dehydrogenase kinases (PDKs). It has been reported to possess a strong lysosomotropic property; this feature enables its assembly inside the acidic compartments within a cell, such as lysosomes, which may eventually hinder endocytosis. In this review, we briefly highlight the varied antineoplastic actions of leelamine that have found implications in pharmacological research, and the numerous intracellular targets affected by this agent that can effectively negate the oncogenic process.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Jung, Y Y" uniqKey="Jung Y">Y.Y. 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Lee</name></author></analytic></biblStruct></listBibl></div1></back></TEI><affiliations><list><country><li>Corée du Sud</li><li>France</li><li>Singapour</li></country><region><li>Région capitale de Séoul</li><li>Île-de-France</li></region><settlement><li>Paris</li><li>Séoul</li></settlement><orgName><li>Université nationale de Singapour</li></orgName></list><tree><country name="France"><region name="Île-de-France"><name sortKey="Merarchi, Myriam" sort="Merarchi, Myriam" uniqKey="Merarchi M" first="Myriam" last="Merarchi">Myriam Merarchi</name></region></country><country name="Singapour"><noRegion><name sortKey="Merarchi, Myriam" sort="Merarchi, Myriam" uniqKey="Merarchi M" first="Myriam" last="Merarchi">Myriam Merarchi</name></noRegion><name sortKey="Fan, Lu" sort="Fan, Lu" uniqKey="Fan L" first="Lu" last="Fan">Lu Fan</name><name sortKey="Sethi, Gautam" sort="Sethi, Gautam" uniqKey="Sethi G" first="Gautam" last="Sethi">Gautam Sethi</name></country><country name="Corée du Sud"><region name="Région capitale de Séoul"><name sortKey="Jung, Young Yun" sort="Jung, Young Yun" uniqKey="Jung Y" first="Young Yun" last="Jung">Young Yun Jung</name></region><name sortKey="Ahn, Kwang Seok" sort="Ahn, Kwang Seok" uniqKey="Ahn K" first="Kwang Seok" last="Ahn">Kwang Seok Ahn</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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