Mito‐Bomb: Targeting Mitochondria for Cancer Therapy

Cancer has been one of the most common life‐threatening diseases for a long time. Traditional cancer therapies such as surgery, chemotherapy (CT), and radiotherapy (RT) have limited effects due to drug resistance, unsatisfactory treatment efficiency, and side effects. In recent years, photodynamic t...

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Published inAdvanced materials (Weinheim) Vol. 33; no. 43; pp. e2007778 - n/a
Main Authors Guo, Xiaolu, Yang, Naidi, Ji, Wenhui, Zhang, Hang, Dong, Xiao, Zhou, Zhiqiang, Li, Lin, Shen, Han‐Ming, Yao, Shao Q., Huang, Wei
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 01.10.2021
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Abstract Cancer has been one of the most common life‐threatening diseases for a long time. Traditional cancer therapies such as surgery, chemotherapy (CT), and radiotherapy (RT) have limited effects due to drug resistance, unsatisfactory treatment efficiency, and side effects. In recent years, photodynamic therapy (PDT), photothermal therapy (PTT), and chemodynamic therapy (CDT) have been utilized for cancer treatment owing to their high selectivity, minor resistance, and minimal toxicity. Accumulating evidence has demonstrated that selective delivery of drugs to specific subcellular organelles can significantly enhance the efficiency of cancer therapy. Mitochondria‐targeting therapeutic strategies are promising for cancer therapy, which is attributed to the essential role of mitochondria in the regulation of cancer cell apoptosis, metabolism, and more vulnerable to hyperthermia and oxidative damage. Herein, the rational design, functionalization, and applications of diverse mitochondria‐targeting units, involving organic phosphine/sulfur salts, quaternary ammonium (QA) salts, peptides, transition‐metal complexes, guanidinium or bisguanidinium, as well as mitochondria‐targeting cancer therapies including PDT, PTT, CDT, and others are summarized. This review aims to furnish researchers with deep insights and hints in the design and applications of novel mitochondria‐targeting agents for cancer therapy. The concept of “Mito‐Bomb Tumor Therapy” is proposed from an interdisciplinary perspective of “biology–chemistry–materials,” and the biological functions of mitochondria, mitochondria‐targeting functional units, and various cancer treatment strategies that target mitochondria, including but not limited to photothermal therapy, photodynamic therapy, and chemodynamic therapy are summarized in detail.
AbstractList Cancer has been one of the most common life‐threatening diseases for a long time. Traditional cancer therapies such as surgery, chemotherapy (CT), and radiotherapy (RT) have limited effects due to drug resistance, unsatisfactory treatment efficiency, and side effects. In recent years, photodynamic therapy (PDT), photothermal therapy (PTT), and chemodynamic therapy (CDT) have been utilized for cancer treatment owing to their high selectivity, minor resistance, and minimal toxicity. Accumulating evidence has demonstrated that selective delivery of drugs to specific subcellular organelles can significantly enhance the efficiency of cancer therapy. Mitochondria‐targeting therapeutic strategies are promising for cancer therapy, which is attributed to the essential role of mitochondria in the regulation of cancer cell apoptosis, metabolism, and more vulnerable to hyperthermia and oxidative damage. Herein, the rational design, functionalization, and applications of diverse mitochondria‐targeting units, involving organic phosphine/sulfur salts, quaternary ammonium (QA) salts, peptides, transition‐metal complexes, guanidinium or bisguanidinium, as well as mitochondria‐targeting cancer therapies including PDT, PTT, CDT, and others are summarized. This review aims to furnish researchers with deep insights and hints in the design and applications of novel mitochondria‐targeting agents for cancer therapy.
Cancer has been one of the most common life‐threatening diseases for a long time. Traditional cancer therapies such as surgery, chemotherapy (CT), and radiotherapy (RT) have limited effects due to drug resistance, unsatisfactory treatment efficiency, and side effects. In recent years, photodynamic therapy (PDT), photothermal therapy (PTT), and chemodynamic therapy (CDT) have been utilized for cancer treatment owing to their high selectivity, minor resistance, and minimal toxicity. Accumulating evidence has demonstrated that selective delivery of drugs to specific subcellular organelles can significantly enhance the efficiency of cancer therapy. Mitochondria‐targeting therapeutic strategies are promising for cancer therapy, which is attributed to the essential role of mitochondria in the regulation of cancer cell apoptosis, metabolism, and more vulnerable to hyperthermia and oxidative damage. Herein, the rational design, functionalization, and applications of diverse mitochondria‐targeting units, involving organic phosphine/sulfur salts, quaternary ammonium (QA) salts, peptides, transition‐metal complexes, guanidinium or bisguanidinium, as well as mitochondria‐targeting cancer therapies including PDT, PTT, CDT, and others are summarized. This review aims to furnish researchers with deep insights and hints in the design and applications of novel mitochondria‐targeting agents for cancer therapy. The concept of “Mito‐Bomb Tumor Therapy” is proposed from an interdisciplinary perspective of “biology–chemistry–materials,” and the biological functions of mitochondria, mitochondria‐targeting functional units, and various cancer treatment strategies that target mitochondria, including but not limited to photothermal therapy, photodynamic therapy, and chemodynamic therapy are summarized in detail.
Cancer has been one of the most common life-threatening diseases for a long time. Traditional cancer therapies such as surgery, chemotherapy (CT), and radiotherapy (RT) have limited effects due to drug resistance, unsatisfactory treatment efficiency, and side effects. In recent years, photodynamic therapy (PDT), photothermal therapy (PTT), and chemodynamic therapy (CDT) have been utilized for cancer treatment owing to their high selectivity, minor resistance, and minimal toxicity. Accumulating evidence has demonstrated that selective delivery of drugs to specific subcellular organelles can significantly enhance the efficiency of cancer therapy. Mitochondria-targeting therapeutic strategies are promising for cancer therapy, which is attributed to the essential role of mitochondria in the regulation of cancer cell apoptosis, metabolism, and more vulnerable to hyperthermia and oxidative damage. Herein, the rational design, functionalization, and applications of diverse mitochondria-targeting units, involving organic phosphine/sulfur salts, quaternary ammonium (QA) salts, peptides, transition-metal complexes, guanidinium or bisguanidinium, as well as mitochondria-targeting cancer therapies including PDT, PTT, CDT, and others are summarized. This review aims to furnish researchers with deep insights and hints in the design and applications of novel mitochondria-targeting agents for cancer therapy.Cancer has been one of the most common life-threatening diseases for a long time. Traditional cancer therapies such as surgery, chemotherapy (CT), and radiotherapy (RT) have limited effects due to drug resistance, unsatisfactory treatment efficiency, and side effects. In recent years, photodynamic therapy (PDT), photothermal therapy (PTT), and chemodynamic therapy (CDT) have been utilized for cancer treatment owing to their high selectivity, minor resistance, and minimal toxicity. Accumulating evidence has demonstrated that selective delivery of drugs to specific subcellular organelles can significantly enhance the efficiency of cancer therapy. Mitochondria-targeting therapeutic strategies are promising for cancer therapy, which is attributed to the essential role of mitochondria in the regulation of cancer cell apoptosis, metabolism, and more vulnerable to hyperthermia and oxidative damage. Herein, the rational design, functionalization, and applications of diverse mitochondria-targeting units, involving organic phosphine/sulfur salts, quaternary ammonium (QA) salts, peptides, transition-metal complexes, guanidinium or bisguanidinium, as well as mitochondria-targeting cancer therapies including PDT, PTT, CDT, and others are summarized. This review aims to furnish researchers with deep insights and hints in the design and applications of novel mitochondria-targeting agents for cancer therapy.
Author Ji, Wenhui
Li, Lin
Dong, Xiao
Shen, Han‐Ming
Huang, Wei
Guo, Xiaolu
Yang, Naidi
Zhang, Hang
Zhou, Zhiqiang
Yao, Shao Q.
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  surname: Guo
  fullname: Guo, Xiaolu
  organization: Nanjing Tech University (NanjingTech)
– sequence: 2
  givenname: Naidi
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  fullname: Yang, Naidi
  organization: Nanjing Tech University (NanjingTech)
– sequence: 3
  givenname: Wenhui
  surname: Ji
  fullname: Ji, Wenhui
  organization: Nanjing Tech University (NanjingTech)
– sequence: 4
  givenname: Hang
  surname: Zhang
  fullname: Zhang, Hang
  organization: Nanjing Tech University (NanjingTech)
– sequence: 5
  givenname: Xiao
  surname: Dong
  fullname: Dong, Xiao
  organization: National University of Singapore
– sequence: 6
  givenname: Zhiqiang
  surname: Zhou
  fullname: Zhou, Zhiqiang
  organization: Nanjing Tech University (NanjingTech)
– sequence: 7
  givenname: Lin
  surname: Li
  fullname: Li, Lin
  email: iamlli@njtech.edu.cn
  organization: Nanjing Tech University (NanjingTech)
– sequence: 8
  givenname: Han‐Ming
  surname: Shen
  fullname: Shen, Han‐Ming
  organization: University of Macau
– sequence: 9
  givenname: Shao Q.
  surname: Yao
  fullname: Yao, Shao Q.
  email: chmyaosq@nus.edu.sg
  organization: National University of Singapore
– sequence: 10
  givenname: Wei
  orcidid: 0000-0001-7004-6408
  surname: Huang
  fullname: Huang, Wei
  email: iamwhuang@njtech.edu.cn
  organization: Northwestern Polytechnical University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/34510563$$D View this record in MEDLINE/PubMed
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2003; 3
2020; 49
2010; 397
1995; 322
2016; 116
2020; 44
2018; 77
2014; 50
2012; 337
2008; 60
2001; 14
2014; 6
2007; 26
2003; 88
2014; 53
2014; 289
2021; 9
2007; 129
2015; 6
2015; 5
2015; 4
2015; 3
2013; 49
2013; 46
2019; 76
2013; 45
2013; 42
2017; 23
2020; 105
2016; 1866
2017; 29
2020; 101
2015; 9
2004; 91
2015; 8
2015; 7
2020; 229
2016; 240
2004; 98
2011; 102
2014; 505
2019; 85
2020; 231
2017; 17
2013; 34
2018; 552
2020; 70
2017; 10
2017; 13
2020; 115
2020; 232
2016; 138
2017; 18
2020; 66
2009; 4
2009; 3
2003; 421
2018; 54
2014; 71
2001; 478
1956; 123
2018; 57
2015; 79
2013; 3
2013; 4
2020; 203
2014; 26
2014; 24
2020; 99
2020; 322
2018; 45
2013; 5
2003; 552
2014; 136
2018; 47
2013; 9
2018; 9
2010; 21
2009; 14
2018; 8
2018; 3
2018; 2
2018; 5
2009; 10
2007; 9
2007; 2
1998; 94
2003; 43
2014; 11
1989; 3
2019; 8
2019; 7
2015; 56
2018; 29
2010; 31
2019; 9
2018; 28
2019; 6
2010; 39
2015; 53
2005; 117
2007; 96
2018; 23
2018; 22
2018; 26
2003; 32
2018; 19
2018; 18
2010; 43
2010; 49
2010; 47
2003; 348
2012; 112
2005; 120
2015; 60
2006; 49
2019; 213
2014; 35
2018; 12
2014; 30
2003; 103
2016; 291
2018; 10
2014; 384
2020; 318
2018; 16
2018; 14
2014; 31
2017; 5
2017; 6
2017; 7
2017; 8
2015; 36
2004; 126
2017; 3
2015; 31
2000; 7
2011; 13
2011; 12
2011; 17
2011; 16
2017; 9
2009; 53
2015; 44
2011; 22
2016; 84
2019; 119
2011; 23
2005; 39
2001; 98
2020; 418
2015; 12
2015; 15
2018; 144
2015; 14
2015; 16
2018; 140
1984; 81
2009; 20
2021; 500
2008; 19
2020; 181
2018; 148
2015; 10
2006; 7
2008; 12
2006; 5
2020; 189
1999; 2
2017; 176
2019; 141
2014; 114
2008; 283
2016; 55
2018; 153
2021; 14
2021; 13
2012; 393
2004; 11
2018; 155
2015; 26
2015; 25
2012; 2
2009; 30
2018; 157
2011; 50
2016; 62
2001; 3
2005; 50
1999; 434
2012; 5
2014; 103
2012; 8
2019; 132
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Zhan X. K. (e_1_2_10_280_1) 2018; 16
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Zini R. (e_1_2_10_282_1) 1999; 2
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Snippet Cancer has been one of the most common life‐threatening diseases for a long time. Traditional cancer therapies such as surgery, chemotherapy (CT), and...
Cancer has been one of the most common life-threatening diseases for a long time. Traditional cancer therapies such as surgery, chemotherapy (CT), and...
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SubjectTerms Animals
Antineoplastic Agents - chemistry
Antineoplastic Agents - pharmacology
Antineoplastic Agents - therapeutic use
Apoptosis
Cancer
Cancer therapies
cancer therapy
chemodynamic therapy
Coordination compounds
Humans
Hyperthermia
Mitochondria
Mitochondria - drug effects
Mitochondria - metabolism
Neoplasms - drug therapy
Neoplasms - metabolism
Neoplasms - pathology
Organelles
Peptides
Phosphines
Photochemotherapy - methods
Photodynamic therapy
photothermal therapy
Radiation therapy
Selectivity
Side effects
Toxicity
Title Mito‐Bomb: Targeting Mitochondria for Cancer Therapy
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fadma.202007778
https://www.ncbi.nlm.nih.gov/pubmed/34510563
https://www.proquest.com/docview/2585378362
https://www.proquest.com/docview/2572231654
Volume 33
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