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Gold (III) Derivatives in Colon Cancer Treatment
Cancer is one of the leading causes of morbidity and mortality worldwide. Colorectal cancer (CRC) is the third most frequently diagnosed cancer in men and the second in women. Standard patterns of antitumor therapy, including cisplatin, are ineffective due to their lack of specificity for tumor cell...
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Published in: | International journal of molecular sciences 2022-01, Vol.23 (2), p.724 |
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description | Cancer is one of the leading causes of morbidity and mortality worldwide. Colorectal cancer (CRC) is the third most frequently diagnosed cancer in men and the second in women. Standard patterns of antitumor therapy, including cisplatin, are ineffective due to their lack of specificity for tumor cells, development of drug resistance, and severe side effects. For this reason, new methods and strategies for CRC treatment are urgently needed. Current research includes novel platinum (Pt)- and other metal-based drugs such as gold (Au), silver (Ag), iridium (Ir), or ruthenium (Ru). Au(III) compounds are promising drug candidates for CRC treatment due to their structural similarity to Pt(II). Their advantage is their relatively good solubility in water, but their disadvantage is an unsatisfactory stability under physiological conditions. Due to these limitations, work is still underway to improve the formula of Au(III) complexes by combining with various types of ligands capable of stabilizing the Au(III) cation and preventing its reduction under physiological conditions. This review summarizes the achievements in the field of stable Au(III) complexes with potential cytotoxic activity restricted to cancer cells. Moreover, it has been shown that not nucleic acids but various protein structures such as thioredoxin reductase (TrxR) mediate the antitumor effects of Au derivatives. The state of the art of the in vivo studies so far conducted is also described. |
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Colorectal cancer (CRC) is the third most frequently diagnosed cancer in men and the second in women. Standard patterns of antitumor therapy, including cisplatin, are ineffective due to their lack of specificity for tumor cells, development of drug resistance, and severe side effects. For this reason, new methods and strategies for CRC treatment are urgently needed. Current research includes novel platinum (Pt)- and other metal-based drugs such as gold (Au), silver (Ag), iridium (Ir), or ruthenium (Ru). Au(III) compounds are promising drug candidates for CRC treatment due to their structural similarity to Pt(II). Their advantage is their relatively good solubility in water, but their disadvantage is an unsatisfactory stability under physiological conditions. Due to these limitations, work is still underway to improve the formula of Au(III) complexes by combining with various types of ligands capable of stabilizing the Au(III) cation and preventing its reduction under physiological conditions. This review summarizes the achievements in the field of stable Au(III) complexes with potential cytotoxic activity restricted to cancer cells. Moreover, it has been shown that not nucleic acids but various protein structures such as thioredoxin reductase (TrxR) mediate the antitumor effects of Au derivatives. The state of the art of the in vivo studies so far conducted is also described.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms23020724</identifier><identifier>PMID: 35054907</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Aging ; Animals ; Antineoplastic Agents - chemistry ; Antineoplastic Agents - pharmacology ; Antineoplastic Agents - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Antitumor activity ; Bioavailability ; Biomarkers ; Cancer therapies ; Chemotherapy ; Cisplatin ; Clinical Studies as Topic ; Colon ; Colon cancer ; Colonic Neoplasms - diagnosis ; Colonic Neoplasms - drug therapy ; Colonic Neoplasms - etiology ; Colonic Neoplasms - metabolism ; Colorectal cancer ; Colorectal carcinoma ; Combined Modality Therapy ; Coordination Complexes - chemistry ; Coordination Complexes - pharmacology ; Coordination Complexes - therapeutic use ; Cytotoxicity ; Disease ; Disease Management ; Disease Susceptibility ; Dose-Response Relationship, Drug ; Drug development ; Drug Development - methods ; Drug Evaluation, Preclinical ; Drug resistance ; Gold ; Gold - chemistry ; Humans ; In vivo methods and tests ; Industrialized nations ; Metals ; Metastasis ; Molecular Structure ; Morbidity ; Mutation ; Nanoparticles ; Neoplasm Metastasis ; Neoplasm Staging ; Nucleic acids ; Physiology ; Reductases ; Review ; Ruthenium ; Signal Transduction - drug effects ; Silver ; Structure-Activity Relationship ; Surgery ; Thioredoxin ; Tumor cells ; Tumors</subject><ispartof>International journal of molecular sciences, 2022-01, Vol.23 (2), p.724</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-25b7747a5f8a930e2a279c887e439edc4c852fb95799a6b41ee7dde7402440a3</citedby><cites>FETCH-LOGICAL-c412t-25b7747a5f8a930e2a279c887e439edc4c852fb95799a6b41ee7dde7402440a3</cites><orcidid>0000-0002-8443-4417 ; 0000-0003-2874-8056 ; 0000-0002-5192-6415</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2621326378/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2621326378?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25744,27915,27916,37003,44581,53782,53784,74887</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35054907$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gurba, Agata</creatorcontrib><creatorcontrib>Taciak, Przemysław</creatorcontrib><creatorcontrib>Sacharczuk, Mariusz</creatorcontrib><creatorcontrib>Młynarczuk-Biały, Izabela</creatorcontrib><creatorcontrib>Bujalska-Zadrożny, Magdalena</creatorcontrib><creatorcontrib>Fichna, Jakub</creatorcontrib><title>Gold (III) Derivatives in Colon Cancer Treatment</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Cancer is one of the leading causes of morbidity and mortality worldwide. Colorectal cancer (CRC) is the third most frequently diagnosed cancer in men and the second in women. Standard patterns of antitumor therapy, including cisplatin, are ineffective due to their lack of specificity for tumor cells, development of drug resistance, and severe side effects. For this reason, new methods and strategies for CRC treatment are urgently needed. Current research includes novel platinum (Pt)- and other metal-based drugs such as gold (Au), silver (Ag), iridium (Ir), or ruthenium (Ru). Au(III) compounds are promising drug candidates for CRC treatment due to their structural similarity to Pt(II). Their advantage is their relatively good solubility in water, but their disadvantage is an unsatisfactory stability under physiological conditions. Due to these limitations, work is still underway to improve the formula of Au(III) complexes by combining with various types of ligands capable of stabilizing the Au(III) cation and preventing its reduction under physiological conditions. This review summarizes the achievements in the field of stable Au(III) complexes with potential cytotoxic activity restricted to cancer cells. Moreover, it has been shown that not nucleic acids but various protein structures such as thioredoxin reductase (TrxR) mediate the antitumor effects of Au derivatives. The state of the art of the in vivo studies so far conducted is also described.</description><subject>Aging</subject><subject>Animals</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Antitumor activity</subject><subject>Bioavailability</subject><subject>Biomarkers</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Cisplatin</subject><subject>Clinical Studies as Topic</subject><subject>Colon</subject><subject>Colon cancer</subject><subject>Colonic Neoplasms - diagnosis</subject><subject>Colonic Neoplasms - drug therapy</subject><subject>Colonic Neoplasms - etiology</subject><subject>Colonic Neoplasms - metabolism</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Combined Modality Therapy</subject><subject>Coordination Complexes - 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Colorectal cancer (CRC) is the third most frequently diagnosed cancer in men and the second in women. Standard patterns of antitumor therapy, including cisplatin, are ineffective due to their lack of specificity for tumor cells, development of drug resistance, and severe side effects. For this reason, new methods and strategies for CRC treatment are urgently needed. Current research includes novel platinum (Pt)- and other metal-based drugs such as gold (Au), silver (Ag), iridium (Ir), or ruthenium (Ru). Au(III) compounds are promising drug candidates for CRC treatment due to their structural similarity to Pt(II). Their advantage is their relatively good solubility in water, but their disadvantage is an unsatisfactory stability under physiological conditions. Due to these limitations, work is still underway to improve the formula of Au(III) complexes by combining with various types of ligands capable of stabilizing the Au(III) cation and preventing its reduction under physiological conditions. This review summarizes the achievements in the field of stable Au(III) complexes with potential cytotoxic activity restricted to cancer cells. Moreover, it has been shown that not nucleic acids but various protein structures such as thioredoxin reductase (TrxR) mediate the antitumor effects of Au derivatives. The state of the art of the in vivo studies so far conducted is also described.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35054907</pmid><doi>10.3390/ijms23020724</doi><orcidid>https://orcid.org/0000-0002-8443-4417</orcidid><orcidid>https://orcid.org/0000-0003-2874-8056</orcidid><orcidid>https://orcid.org/0000-0002-5192-6415</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aging Animals Antineoplastic Agents - chemistry Antineoplastic Agents - pharmacology Antineoplastic Agents - therapeutic use Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use Antitumor activity Bioavailability Biomarkers Cancer therapies Chemotherapy Cisplatin Clinical Studies as Topic Colon Colon cancer Colonic Neoplasms - diagnosis Colonic Neoplasms - drug therapy Colonic Neoplasms - etiology Colonic Neoplasms - metabolism Colorectal cancer Colorectal carcinoma Combined Modality Therapy Coordination Complexes - chemistry Coordination Complexes - pharmacology Coordination Complexes - therapeutic use Cytotoxicity Disease Disease Management Disease Susceptibility Dose-Response Relationship, Drug Drug development Drug Development - methods Drug Evaluation, Preclinical Drug resistance Gold Gold - chemistry Humans In vivo methods and tests Industrialized nations Metals Metastasis Molecular Structure Morbidity Mutation Nanoparticles Neoplasm Metastasis Neoplasm Staging Nucleic acids Physiology Reductases Review Ruthenium Signal Transduction - drug effects Silver Structure-Activity Relationship Surgery Thioredoxin Tumor cells Tumors |
title | Gold (III) Derivatives in Colon Cancer Treatment |
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