Targeted drug delivery systems for elemene in cancer therapy: The story thus far.

Huan Tian,Feng Zhao, Qing-Rui Qi, Bao-Sen Yue,Bing-Tao Zhai

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie(2023)

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摘要
Elemene (ELE) is a group of broad-spectrum anticancer active ingredients with low toxicity extracted from traditional Chinese medicines (TCMs), such as Curcumae Rhizoma and Curcuma Radix, which can exert antitumour activities by regulating various signal pathways and targets. However, the strong hydrophobicity, short half-life, low bioavailability and weak in vivo targeting ability of ELE restrict its use. Targeted drug delivery systems based on nanomaterials are among the most viable methods to overcome these shortcomings. In this review, we first summarize recent studies on the clinical uses of ELE as an adjunct antitumour drug. ELE-based combination strategies have great promise for enhancing efficacy, reducing adverse reactions, and improving patients' quality of life and immune function. Second, we summarize recent studies on the antitumour mechanisms of ELE and ELE-based combination strategies. The potential mechanisms include inducing pyroptosis and ferroptosis, promoting senescence, regulating METTL3-mediated mA modification, suppressing the Warburg effect, and inducing apoptosis and cell cycle arrest. Most importantly, we comprehensively summarize studies on the combination of targeted drug delivery systems with ELE, including passively and actively targeted drug delivery systems, stimuli-responsive drug delivery systems, and codelivery systems for ELE combined with other therapies, which have great promise in improving drug bioavailability, increasing drug targeting ability, controlling drug release, enhancing drug efficacy, reducing drug adverse effects and reversing MDR. Our summary will provide a reference for the combination of TCMs such as ELE with advanced targeted drug delivery systems in the future.
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ELE,TCMs,β-E,MDR,ORR,TACE,NSCLC,ROS,PEG,AsNDs@PEG,NIR,EPR effect,RES,DSPE-PEG2000,EE,mPEG-PCL,AUC,Re,PVP,t1/2,MRT,PEG-Lipo-β-E,SLN,PEG-SLN,SLN-β,BBB,NLC,β-E-NLC,CL,PBCA,β-E-PBCA-NP,Cmax,β-E-N,SEDDS,FRs,FA,FA-PEG-SLN,FA-PEG2000-DOPE,TfRs,Tf,TF-EC-ME,ALT,AST,UA,BUN,CREA,uPAR,uPA,ATF24-PEG-Lipo-β-E,CD44,HA,DOX,MSN,bMED NPs,EpcAM,PTX,SYL3C/EP-ME,SR-B1,HDL,Apo A1,SOR,AA-S-E-LP,CMP,Tf-ELE/CTX@LIP,Tf-ELE/CTX@BLIP,P-gp,Tm,HT,TLLE,PDA,D/MSN-ELE,DOPE,PAA,Ele/MSNs-PAA,DOX/ELE Hyd NLCs,SDT,DDP,β-ELE-DDP-LPs,DOX/ELE NLCs,EP-ME,MTO,MTO/βE SLNs,PEG-S-E-LP,EC-ME,pTA,Ele-PLGA-pTA NPs,IR780-Ele-LCL,SnNSs@PEG-E,LEAg,LAg,NDV,LEVAg,LVAg,TAM,NGO
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