Enzymatic synthesis of DHA-lysophosphatidylcholine and evaluation of its effect on the MDA-MB-231 human breast cancer cell line

This work studies the synthesis of DHA-lysophosphatidylcholine (LPC-DHA) by solvent-free lipase-catalyzed esterification and the ability of LPC-DHA to reduce cell viability of the human cancer cell line MDA-MB-231. Optimization of esterification parameters between glycerophosphatidylcholine (GPC) an...

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Main Author: Mohamad Ali, Dalal
Other Authors: Biologie des Organismes, Stress, Santé, Environnement Le Mans Université (BiOSSE), Le Mans Université (UM), Collectivités Locales Mayennaises, Le Mans Université, Lionel Ulmann, Gaëlle Pencreac'h, Laurent Poisson
Format: Doctoral or Postdoctoral Thesis
Language:English
Published: HAL CCSD 2022
Subjects:
Online Access:https://hal.science/tel-04102506
https://hal.science/tel-04102506/document
https://hal.science/tel-04102506/file/Dalal%20Mohamad%20Ali%20-%20manuscrit%20du%20th%C3%A9se%202022.pdf
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spelling ftccsdartic:oai:HAL:tel-04102506v1 2024-02-11T09:56:13+01:00 Enzymatic synthesis of DHA-lysophosphatidylcholine and evaluation of its effect on the MDA-MB-231 human breast cancer cell line Synthèse enzymatique de la DHA-lysophosphatidylcholine et évaluation de son effet sur la lignée cellulaire de cancer du sein humain MDA-MB 231 Mohamad Ali, Dalal Biologie des Organismes, Stress, Santé, Environnement Le Mans Université (BiOSSE) Le Mans Université (UM) Collectivités Locales Mayennaises Le Mans Université Lionel Ulmann Gaëlle Pencreac'h Laurent Poisson 2022-02-02 https://hal.science/tel-04102506 https://hal.science/tel-04102506/document https://hal.science/tel-04102506/file/Dalal%20Mohamad%20Ali%20-%20manuscrit%20du%20th%C3%A9se%202022.pdf en eng HAL CCSD NNT: 2022LEMA1003 tel-04102506 https://hal.science/tel-04102506 https://hal.science/tel-04102506/document https://hal.science/tel-04102506/file/Dalal%20Mohamad%20Ali%20-%20manuscrit%20du%20th%C3%A9se%202022.pdf info:eu-repo/semantics/OpenAccess https://hal.science/tel-04102506 Biochemistry, Molecular Biology. Le Mans Université, 2022. English. ⟨NNT : 2022LEMA1003⟩ DHA-lysophosphatidylcholine Solvent free esterification Immobilized lipase Design of experiments (RSM) MDA-MB-231 cell line Breast cancer Cell death mechanisms Docosahexaenoic ω3 polyunsaturated fatty acid Responce surface methodology Estérification sans solvant Plan d’expérience (RSM) Lignée cellulaire MDA-MB-231 Cancer du sein Mort cellulaire Synthèse enzymatique Méthode de réponse de surface [SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology [SDV.BC]Life Sciences [q-bio]/Cellular Biology [SDV.BIO]Life Sciences [q-bio]/Biotechnology info:eu-repo/semantics/doctoralThesis Theses 2022 ftccsdartic 2024-01-13T23:57:14Z This work studies the synthesis of DHA-lysophosphatidylcholine (LPC-DHA) by solvent-free lipase-catalyzed esterification and the ability of LPC-DHA to reduce cell viability of the human cancer cell line MDA-MB-231. Optimization of esterification parameters between glycerophosphatidylcholine (GPC) and docosahexaenoic acid (DHA) was performed using response surface methodology (RSM). Two responses were measured: the conversion yield of GPC and the concentration of LPC-DHA in the medium. A GPC conversion yield of 67% is obtained under the following reaction conditions: a DHA/GPC molar ratio of 17, a reaction temperature of 36°C and a Novozym® 435 (immobilized lipase B from Candida antarctica) load of 15%. The maximum concentration of LPC-DHA obtained is 245 mM under the following conditions: a DHA/GPC molar ratio of 4, temperature of 36°C and a Novozym® 435 load of 15%. NMR characterization confirmed that the synthesized compound is pure and unoxidized sn-1 LPC-DHA In vitro study of the effect of different LPCs and different lipid vectors of DHA on MDA-MB-231 showed that LPC-DHA was the most effective in reducing cell viability, with IC50 for LPC-DHA, PC-DHA, MAG-DHA, and free DHA of 19 µM, 50 µM, 170 µM, and 347 µM, respectively. LPC-DHA and PC-DHA reduce cell viability primarily by inducing oxidative stress and plasma membrane damage. DHA and MAG-DHA also induced oxidative stress. In conclusion, this work led to the synthesis of LPC-DHA under favorable conditions and demonstrated the very interesting effect of LPC-DHA in reducing the viability of MDA-MB-231 breast cancer cells. Ce travail étudie la synthèse de DHA-lysophosphatidylcholine (LPC-DHA) par estérification enzymatique, catalysée par une lipase et sans solvant, ainsi que la capacité de la LPC-DHA à réduire la viabilité cellulaire de la lignée cancéreuse humaine MDA-MB-231. Une optimisation des paramètres de l’estérification entre la glycerophosphatidylcholine (GPC) et l’acide docosahexaénoïque (DHA, C22 :6 ω-3) a été réalisée selon la méthodologie des ... Doctoral or Postdoctoral Thesis Antarc* Antarctica Archive ouverte HAL (Hyper Article en Ligne, CCSD - Centre pour la Communication Scientifique Directe)
institution Open Polar
collection Archive ouverte HAL (Hyper Article en Ligne, CCSD - Centre pour la Communication Scientifique Directe)
op_collection_id ftccsdartic
language English
topic DHA-lysophosphatidylcholine
Solvent free esterification
Immobilized lipase
Design of experiments (RSM)
MDA-MB-231 cell line
Breast cancer
Cell death mechanisms
Docosahexaenoic ω3 polyunsaturated fatty acid
Responce surface methodology
Estérification sans solvant
Plan d’expérience (RSM)
Lignée cellulaire MDA-MB-231
Cancer du sein
Mort cellulaire
Synthèse enzymatique
Méthode de réponse de surface
[SDV.BBM]Life Sciences [q-bio]/Biochemistry
Molecular Biology
[SDV.BC]Life Sciences [q-bio]/Cellular Biology
[SDV.BIO]Life Sciences [q-bio]/Biotechnology
spellingShingle DHA-lysophosphatidylcholine
Solvent free esterification
Immobilized lipase
Design of experiments (RSM)
MDA-MB-231 cell line
Breast cancer
Cell death mechanisms
Docosahexaenoic ω3 polyunsaturated fatty acid
Responce surface methodology
Estérification sans solvant
Plan d’expérience (RSM)
Lignée cellulaire MDA-MB-231
Cancer du sein
Mort cellulaire
Synthèse enzymatique
Méthode de réponse de surface
[SDV.BBM]Life Sciences [q-bio]/Biochemistry
Molecular Biology
[SDV.BC]Life Sciences [q-bio]/Cellular Biology
[SDV.BIO]Life Sciences [q-bio]/Biotechnology
Mohamad Ali, Dalal
Enzymatic synthesis of DHA-lysophosphatidylcholine and evaluation of its effect on the MDA-MB-231 human breast cancer cell line
topic_facet DHA-lysophosphatidylcholine
Solvent free esterification
Immobilized lipase
Design of experiments (RSM)
MDA-MB-231 cell line
Breast cancer
Cell death mechanisms
Docosahexaenoic ω3 polyunsaturated fatty acid
Responce surface methodology
Estérification sans solvant
Plan d’expérience (RSM)
Lignée cellulaire MDA-MB-231
Cancer du sein
Mort cellulaire
Synthèse enzymatique
Méthode de réponse de surface
[SDV.BBM]Life Sciences [q-bio]/Biochemistry
Molecular Biology
[SDV.BC]Life Sciences [q-bio]/Cellular Biology
[SDV.BIO]Life Sciences [q-bio]/Biotechnology
description This work studies the synthesis of DHA-lysophosphatidylcholine (LPC-DHA) by solvent-free lipase-catalyzed esterification and the ability of LPC-DHA to reduce cell viability of the human cancer cell line MDA-MB-231. Optimization of esterification parameters between glycerophosphatidylcholine (GPC) and docosahexaenoic acid (DHA) was performed using response surface methodology (RSM). Two responses were measured: the conversion yield of GPC and the concentration of LPC-DHA in the medium. A GPC conversion yield of 67% is obtained under the following reaction conditions: a DHA/GPC molar ratio of 17, a reaction temperature of 36°C and a Novozym® 435 (immobilized lipase B from Candida antarctica) load of 15%. The maximum concentration of LPC-DHA obtained is 245 mM under the following conditions: a DHA/GPC molar ratio of 4, temperature of 36°C and a Novozym® 435 load of 15%. NMR characterization confirmed that the synthesized compound is pure and unoxidized sn-1 LPC-DHA In vitro study of the effect of different LPCs and different lipid vectors of DHA on MDA-MB-231 showed that LPC-DHA was the most effective in reducing cell viability, with IC50 for LPC-DHA, PC-DHA, MAG-DHA, and free DHA of 19 µM, 50 µM, 170 µM, and 347 µM, respectively. LPC-DHA and PC-DHA reduce cell viability primarily by inducing oxidative stress and plasma membrane damage. DHA and MAG-DHA also induced oxidative stress. In conclusion, this work led to the synthesis of LPC-DHA under favorable conditions and demonstrated the very interesting effect of LPC-DHA in reducing the viability of MDA-MB-231 breast cancer cells. Ce travail étudie la synthèse de DHA-lysophosphatidylcholine (LPC-DHA) par estérification enzymatique, catalysée par une lipase et sans solvant, ainsi que la capacité de la LPC-DHA à réduire la viabilité cellulaire de la lignée cancéreuse humaine MDA-MB-231. Une optimisation des paramètres de l’estérification entre la glycerophosphatidylcholine (GPC) et l’acide docosahexaénoïque (DHA, C22 :6 ω-3) a été réalisée selon la méthodologie des ...
author2 Biologie des Organismes, Stress, Santé, Environnement Le Mans Université (BiOSSE)
Le Mans Université (UM)
Collectivités Locales Mayennaises
Le Mans Université
Lionel Ulmann
Gaëlle Pencreac'h
Laurent Poisson
format Doctoral or Postdoctoral Thesis
author Mohamad Ali, Dalal
author_facet Mohamad Ali, Dalal
author_sort Mohamad Ali, Dalal
title Enzymatic synthesis of DHA-lysophosphatidylcholine and evaluation of its effect on the MDA-MB-231 human breast cancer cell line
title_short Enzymatic synthesis of DHA-lysophosphatidylcholine and evaluation of its effect on the MDA-MB-231 human breast cancer cell line
title_full Enzymatic synthesis of DHA-lysophosphatidylcholine and evaluation of its effect on the MDA-MB-231 human breast cancer cell line
title_fullStr Enzymatic synthesis of DHA-lysophosphatidylcholine and evaluation of its effect on the MDA-MB-231 human breast cancer cell line
title_full_unstemmed Enzymatic synthesis of DHA-lysophosphatidylcholine and evaluation of its effect on the MDA-MB-231 human breast cancer cell line
title_sort enzymatic synthesis of dha-lysophosphatidylcholine and evaluation of its effect on the mda-mb-231 human breast cancer cell line
publisher HAL CCSD
publishDate 2022
url https://hal.science/tel-04102506
https://hal.science/tel-04102506/document
https://hal.science/tel-04102506/file/Dalal%20Mohamad%20Ali%20-%20manuscrit%20du%20th%C3%A9se%202022.pdf
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_source https://hal.science/tel-04102506
Biochemistry, Molecular Biology. Le Mans Université, 2022. English. ⟨NNT : 2022LEMA1003⟩
op_relation NNT: 2022LEMA1003
tel-04102506
https://hal.science/tel-04102506
https://hal.science/tel-04102506/document
https://hal.science/tel-04102506/file/Dalal%20Mohamad%20Ali%20-%20manuscrit%20du%20th%C3%A9se%202022.pdf
op_rights info:eu-repo/semantics/OpenAccess
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