Targeting sub-cellular organelles for boosting precision photodynamic therapy

被引:9
作者
Attar, Gopal Singh [1 ]
Kumar, Manoj [1 ]
Bhalla, Vandana [1 ]
机构
[1] Guru Nanak Dev Univ, Ctr Adv Studies 1, Dept Chem UGC Sponsored, Amritsar 143005, Punjab, India
关键词
ENDOPLASMIC-RETICULUM STRESS; IMMUNOGENIC CELL-DEATH; OXYGEN SPECIES BURST; IRIDIUM(III) COMPLEXES; DRUG-DELIVERY; LIVING CELLS; CANCER-THERAPY; GENE DELIVERY; IN-VITRO; MITOCHONDRIA;
D O I
10.1039/d4cc02702g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Among various cancer treatment methods, photodynamic therapy has received significant attention due to its non-invasiveness and high efficiency in inhibiting tumour growth. Recently, specific organelle targeting photosensitizers have received increasing interest due to their precise accumulation and ability to trigger organelle-mediated cell death signalling pathways, which greatly reduces the drug dosage, minimizes toxicity, avoids multidrug resistance, and prevents recurrence. In this review, recent advances and representative photosensitizers used in targeted photodynamic therapy on organelles, specifically including the endoplasmic reticulum, Golgi apparatus, mitochondria, nucleus, and lysosomes, have been comprehensively reviewed with a focus on organelle structure and organelle-mediated cell death signalling pathways. Furthermore, a perspective on future research and potential challenges in precision photodynamic therapy has been presented at the end. In this review, recent advances and representative photosensitizers used in organelle targeted photodynamic therapy have been reviewed with a focus on organelle targeting strategies and organelle-mediated cell death signalling pathways.
引用
收藏
页码:11610 / 11624
页数:15
相关论文
共 240 条
[51]   Elimination of the chemotherapy resistant subpopulation of 4T1 mouse breast cancer by haploidentical NK cells cures the vast majority of mice [J].
Frings, Peter W. H. ;
Van Elssen, Catharina H. M. J. ;
Wieten, Lotte ;
Matos, Catarina ;
Hupperets, Pierre S. J. G. ;
Schouten, Harry C. ;
Bos, Gerard M. J. ;
van Gelder, Michel .
BREAST CANCER RESEARCH AND TREATMENT, 2011, 130 (03) :773-781
[52]   Targeting apoptosis for anticancer therapy [J].
Fulda, Simone .
SEMINARS IN CANCER BIOLOGY, 2015, 31 :84-88
[53]   Boosting Cancer Therapy with Organelle-Targeted Nanomaterials [J].
Gao, Peng ;
Pan, Wei ;
Li, Na ;
Tang, Bo .
ACS APPLIED MATERIALS & INTERFACES, 2019, 11 (30) :26529-26558
[54]   Nanoparticles for Cancer Therapy: Current Progress and Challenges [J].
Gavas, Shreelaxmi ;
Quazi, Sameer ;
Karpinski, Tomasz M. .
NANOSCALE RESEARCH LETTERS, 2021, 16 (01)
[55]   SAA1/TLR2 axis directs chemotactic migration of hepatic stellate cells responding to injury [J].
Getachew, Anteneh ;
Abbas, Nasir ;
You, Kai ;
Yang, Zhen ;
Hussain, Muzammal ;
Huang, Xinping ;
Cheng, Ziqi ;
Tan, Shenglin ;
Tao, Jiawang ;
Yu, Xiaorui ;
Chen, Yan ;
Yang, Fan ;
Pan, Tingcai ;
Xu, Yingying ;
Xu, Guosheng ;
Zhuang, Yuanqi ;
Wu, FeiMa ;
Li, Yinxiong .
ISCIENCE, 2021, 24 (05)
[56]   Nanotechnology Meets Stem Cell Therapy for Treating Glioblastomas: A Review [J].
Ghosh, Anup Kumar ;
Ghosh, Aparajita ;
Das, Prasanta Kumar .
ACS APPLIED NANO MATERIALS, 2024, 7 (03) :2430-2460
[57]   The cristal membrane of mitochondria is the principal site of oxidative phosphorylation [J].
Gilkerson, RW ;
Selker, JML ;
Capaldi, RA .
FEBS LETTERS, 2003, 546 (2-3) :355-358
[58]   Finding the Golgi: Golgin Coiled-Coil Proteins Show the Way [J].
Gillingham, Alison K. ;
Munro, Sean .
TRENDS IN CELL BIOLOGY, 2016, 26 (06) :399-408
[59]   Transport between the cell nucleus and the cytoplasm [J].
Görlich, D ;
Kutay, U .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1999, 15 :607-660
[60]   Exploring the Mechanism of Plasmid DNA Nuclear Internalization with Polymer-Based Vehicles [J].
Grandinetti, Giovanna ;
Reineke, Theresa M. .
MOLECULAR PHARMACEUTICS, 2012, 9 (08) :2256-2267