Polyphenol-Rich Date Palm Fruit Seed (<i>Phoenix Dactylifera</i> L.) Extract Inhibits Labile Iron, Enzyme, and Cancer Cell Activities, and DNA and Protein Damage

Date palm fruit seed (<i>Phoenix dactylifera</i> L.) extract (DSE), an under-utilized resource, is a rich source of polyphenols with high potency for disease prevention and antioxidative activities. For the first time, the present study demonstrated that DSE inhibits labile iron activity...

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Main Authors: Hosam M. Habib, Esmail M. El-Fakharany, Usama D. Souka, Fatma M. Elsebaee, Mohamed G. El-Ziney, Wissam H. Ibrahim
Format: Article
Language:English
Published: MDPI AG 2022-08-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/14/17/3536
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author Hosam M. Habib
Esmail M. El-Fakharany
Usama D. Souka
Fatma M. Elsebaee
Mohamed G. El-Ziney
Wissam H. Ibrahim
author_facet Hosam M. Habib
Esmail M. El-Fakharany
Usama D. Souka
Fatma M. Elsebaee
Mohamed G. El-Ziney
Wissam H. Ibrahim
author_sort Hosam M. Habib
collection DOAJ
description Date palm fruit seed (<i>Phoenix dactylifera</i> L.) extract (DSE), an under-utilized resource, is a rich source of polyphenols with high potency for disease prevention and antioxidative activities. For the first time, the present study demonstrated that DSE inhibits labile iron activity and DNA and BSA damage and inhibits acetylcholinesterase and tyrosinase activities. Moreover, DSE reduces the proliferation of hepatic, colorectal, and breast cancer cells dose-dependently through apoptotic mechanisms. Furthermore, DSE significantly suppressed the expression of both BCl-2 and P21 genes and increased the P53 expression level when compared with the untreated cells and the 5-FU treated cells. These findings suggest a strong potential for DSE in protecting against the iron-catalyzed ferroptosis that results in programmed cell death. The results also confirm the efficacy of DSE against cancer cells. Therefore, DSE constitutes a valuable candidate for developing functional foods and for natural compound-based chemotherapy for the pharmaceutical and nutraceutical industries.
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spelling doaj.art-35b9616c92564764b0d043920252d1292023-11-23T13:52:04ZengMDPI AGNutrients2072-66432022-08-011417353610.3390/nu14173536Polyphenol-Rich Date Palm Fruit Seed (<i>Phoenix Dactylifera</i> L.) Extract Inhibits Labile Iron, Enzyme, and Cancer Cell Activities, and DNA and Protein DamageHosam M. Habib0Esmail M. El-Fakharany1Usama D. Souka2Fatma M. Elsebaee3Mohamed G. El-Ziney4Wissam H. Ibrahim5Functional Foods and Nutraceuticals Laboratory (FFNL), Dairy Science and Technology Department, Faculty of Agriculture, Alexandria University, Alexandria P.O. Box 21545, EgyptProtein Research Department, Genetic Engineering and Biotechnology Research Institute GEBRI, City for Scientific Research and Technology Applications, New Borg EL Arab, Alexandria P.O. Box 21934, EgyptDepartment of Nutrition and Health, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain P.O. Box 15551, United Arab EmiratesDepartment of Home Economics, Faculty of Specific Education, Fayoum University, Fayoum P.O. Box 63514, EgyptFunctional Foods and Nutraceuticals Laboratory (FFNL), Dairy Science and Technology Department, Faculty of Agriculture, Alexandria University, Alexandria P.O. Box 21545, EgyptDepartment of Nutrition and Health, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain P.O. Box 15551, United Arab EmiratesDate palm fruit seed (<i>Phoenix dactylifera</i> L.) extract (DSE), an under-utilized resource, is a rich source of polyphenols with high potency for disease prevention and antioxidative activities. For the first time, the present study demonstrated that DSE inhibits labile iron activity and DNA and BSA damage and inhibits acetylcholinesterase and tyrosinase activities. Moreover, DSE reduces the proliferation of hepatic, colorectal, and breast cancer cells dose-dependently through apoptotic mechanisms. Furthermore, DSE significantly suppressed the expression of both BCl-2 and P21 genes and increased the P53 expression level when compared with the untreated cells and the 5-FU treated cells. These findings suggest a strong potential for DSE in protecting against the iron-catalyzed ferroptosis that results in programmed cell death. The results also confirm the efficacy of DSE against cancer cells. Therefore, DSE constitutes a valuable candidate for developing functional foods and for natural compound-based chemotherapy for the pharmaceutical and nutraceutical industries.https://www.mdpi.com/2072-6643/14/17/3536date seed extractlabile iron inhibitionDNA and BSA damageenzyme inhibitionanticancer
spellingShingle Hosam M. Habib
Esmail M. El-Fakharany
Usama D. Souka
Fatma M. Elsebaee
Mohamed G. El-Ziney
Wissam H. Ibrahim
Polyphenol-Rich Date Palm Fruit Seed (<i>Phoenix Dactylifera</i> L.) Extract Inhibits Labile Iron, Enzyme, and Cancer Cell Activities, and DNA and Protein Damage
Nutrients
date seed extract
labile iron inhibition
DNA and BSA damage
enzyme inhibition
anticancer
title Polyphenol-Rich Date Palm Fruit Seed (<i>Phoenix Dactylifera</i> L.) Extract Inhibits Labile Iron, Enzyme, and Cancer Cell Activities, and DNA and Protein Damage
title_full Polyphenol-Rich Date Palm Fruit Seed (<i>Phoenix Dactylifera</i> L.) Extract Inhibits Labile Iron, Enzyme, and Cancer Cell Activities, and DNA and Protein Damage
title_fullStr Polyphenol-Rich Date Palm Fruit Seed (<i>Phoenix Dactylifera</i> L.) Extract Inhibits Labile Iron, Enzyme, and Cancer Cell Activities, and DNA and Protein Damage
title_full_unstemmed Polyphenol-Rich Date Palm Fruit Seed (<i>Phoenix Dactylifera</i> L.) Extract Inhibits Labile Iron, Enzyme, and Cancer Cell Activities, and DNA and Protein Damage
title_short Polyphenol-Rich Date Palm Fruit Seed (<i>Phoenix Dactylifera</i> L.) Extract Inhibits Labile Iron, Enzyme, and Cancer Cell Activities, and DNA and Protein Damage
title_sort polyphenol rich date palm fruit seed i phoenix dactylifera i l extract inhibits labile iron enzyme and cancer cell activities and dna and protein damage
topic date seed extract
labile iron inhibition
DNA and BSA damage
enzyme inhibition
anticancer
url https://www.mdpi.com/2072-6643/14/17/3536
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