Avocado peel extract loaded on chitosan nanoparticles alleviates urethane toxicity that causes lung cancer in a mouse model

被引:8
作者
Sahyon, Heba A. [1 ]
El-Shafai, Nagi M. [2 ]
Elnajjar, Noha [3 ]
Althobaiti, Fayez [4 ]
Aldhahrani, Adil [5 ]
Alharbi, Nadaa S. [6 ,7 ]
Shoair, Abdel Ghany F. [8 ,9 ,10 ]
El-Mehasseb, Ibrahim M. [2 ]
机构
[1] Kafrelsheikh Univ, Fac Sci, Chem Dept, Kafrelsheikh 33516, Egypt
[2] Kafrelsheikh Univ, Fac Sci, Nanotechnol Ctr, Chem Dept, Kafrelsheikh 33516, Egypt
[3] Benha Univ, Fac Med, Forens Med & Clin Toxicol Dept, Benha, Banha, Egypt
[4] Taif Univ, Coll Sci, Dept Biotechnol, POB 11099, Taif 21944, Saudi Arabia
[5] Taif Univ, Turabah Univ Coll, Clin Lab Sci Dept, Taif 21995, Saudi Arabia
[6] Royal Coll Surgeons Ireland, Dublin, Ireland
[7] Minist Hlth, Riyadh, Saudi Arabia
[8] Taif Univ, Univ Coll Ranyah, Dept Sci & Technol, Taif, Saudi Arabia
[9] Damietta Univ, Fac Sci, Dept Chem, Kafr Saad 34517, Egypt
[10] Taif Univ, High Altitude Res Ctr, Prince Sultan Med Complex, Taif, Saudi Arabia
关键词
Avocado peel; Nano-combination; Chitosan; Lung cancer; P53; NF-?B p65; NF-KAPPA-B; THERAPEUTIC TARGET; S-PHASE; APOPTOSIS; ANTICANCER; CELLS; INFLAMMATION; EXPRESSION; MORTALITY; PATHWAY;
D O I
10.1016/j.ijbiomac.2023.123633
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lung cancer progresses without obvious symptoms and is detected in most patients at late stages, causing a high rate of mortality. Avocado peels (AVP) were thought to be biowaste, but they have antioxidant and anticancer properties in vitro. Chitosan nanoparticles (Cs-NPs) were loaded with various plant extracts, increasing their in vitro and in vivo anticancer activities. Our goal was to load AVP onto Cs-NPs and determine the role of AVP-extract or AVP-loaded Cs-NPs in controlling the progression of lung cancer caused by urethane toxicity. The AVP-loaded chitosan nano-combination (Cs@AVP NC) was synthesized and characterized. Our in vitro results show that Cs@AVP NC has higher anticancer activity than AVP against three human cancer cell lines. The in vivo study proved the activation of apoptosis in lung cancer cells with the Cs@AVP NC oral treatment more than the AVP treatment. Additionally, Cs@AVP NC-treated animals showed significantly higher p53 and Bax-expression levels and lower NF-kappa B p65 levels in their lung tissues than in positive control animals. In conclusion, our study demonstrated the superior anticancer potency of Cs@AVP NC over AVP extract and its ability to inhibit lung cancer proliferation. Therefore, oral consumption of Cs@AVP NC might be a promising treatment for lung cancer.
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页数:11
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