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 in | Advanced materials (Weinheim) Vol. 33; no. 43; pp. e2007778 - n/a |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
Wiley Subscription Services, Inc
01.10.2021
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Subjects | |
Online Access | Get full text |
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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. |
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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. |
Author_xml | – sequence: 1 givenname: Xiaolu surname: Guo fullname: Guo, Xiaolu organization: Nanjing Tech University (NanjingTech) – sequence: 2 givenname: Naidi surname: Yang 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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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 |
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