Glutamine metabolism targeting liposomes for synergistic chemosensitization and starvation therapy in ovarian cancer

被引:12
|
作者
Cai, Xuzi [1 ,2 ]
Shi, Si [1 ]
Chen, Gui [3 ]
Zhong, Min [1 ]
Yang, Yuanyuan [4 ]
Mai, Ziyi [3 ]
Tian, Yang [1 ]
Tan, Jinxiu [1 ]
He, Lijuan [1 ]
Cui, Chunhui [5 ]
Yu, Zhiqiang [4 ]
Wang, Xuefeng [1 ]
机构
[1] Southern Med Univ, Dept Obstet & Gynecol, Affiliated Hosp 3, Guangzhou 510632, Peoples R China
[2] Guangzhou Women & Childrens Med Ctr, Dept Obstet & Gynecol, Guangzhou 510623, Peoples R China
[3] Southern Med Univ, Sch Pharmaceut Sci, Guangdong Prov Key Lab New Drug Screening, Guangzhou 510515, Peoples R China
[4] Southern Med Univ, Affiliated Dongguan Hosp, Dept Lab Med, Dongguan 523018, Peoples R China
[5] Southern Med Univ, Zhujiang Hosp, Dept Gen Surg, Guangzhou 510280, Peoples R China
关键词
Glutamine metabolism; Starvation therapy; Chemotherapy; Cisplatin sensitization; Ovarian cancer; IN-VITRO; PROLIFERATION; GLUTATHIONE; SYNTHETASE; COMPLEX;
D O I
10.1016/j.actbio.2022.12.052
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Platinum-based chemotherapy is a first-line therapeutic regimen against ovarian cancer (OC); however, the therapeutic potential is always reduced by glutamine metabolism. Herein, a valid strategy of inhibit-ing glutamine metabolism was proposed to cause tumor starvation and chemosensitization. Specifically, reactive oxygen species-responsive liposomes were developed to co-deliver cisplatin (CDDP) and bis-2-(5-phenylacetamido-1,3,4-thiadiazol-2-yl) ethyl sulfide (BPTES) [C@B LPs]. The C@B LPs induced effective tumor cell starvation and significantly sensitized OC cells to CDDP by reducing glutathione generation to prevent CDDP detoxification, suppressing ATP production to avoid CDDP efflux, hindering nucleotide syn-thesis to aggravate DNA damage induced by CDDP, and blocking mammalian target of rapamycin (mTOR) signaling to promote cell apoptosis. More importantly, C@B LPs remarkably inhibited tumor growth in vivo and reduced the side effects. Taken together, this study provided a successful strategy of synergistic chemosensitization and starvation therapy escalating the rate of therapeutic success in OCs.Statement of significance This work proposed a valid strategy of inhibiting glutamine metabolism to cause tumor starvation and chemosensitization. Specifically, ROS-responsive liposomes were developed to co-deliver cisplatin CDDP and BPTES [C@B LPs]. The C@B LPs induced effective tumor cell starvation and significantly sensitized OC cells to cisplatin by reducing glutathione generation to prevent cisplatin detoxification, suppressing ATP production to avoid cisplatin efflux, hindering nucleotide synthesis to aggravate DNA damage induced by cisplatin, and blocking mTOR signaling to promote cell apoptosis. More importantly, C@B LPs remarkably inhibited tumor growth in vivo and reduced the side effects. Taken together, this study provided a suc-cessful strategy of synergistic chemosensitization and starvation therapy escalating the rate of therapeutic success in OCs.(c) 2022 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:560 / 570
页数:11
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