Dithiocarbazate–Fe III , −Co III , −Ni II , and −Zn II Complexes: Design, Synthesis, Structure, and Anticancer Evaluation
Non-platinum-metal complexes show great potential as anticancer agents. Herein, a series of dithiocarbazate non-Pt-metal complexes, including [Fe (L) ]·Cl·2H O , [Co (L) ]·NO ·2.5H O , [Ni (L) ] , and [Zn (L) ] , have been designed and evaluated for their efficacy as antineoplastic agents. Among the...
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Published in | Journal of medicinal chemistry Vol. 65; no. 9; pp. 6677 - 6689 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
12.05.2022
|
Online Access | Get full text |
ISSN | 0022-2623 1520-4804 |
DOI | 10.1021/acs.jmedchem.1c02186 |
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Abstract | Non-platinum-metal complexes show great potential as anticancer agents. Herein, a series of dithiocarbazate non-Pt-metal complexes, including [Fe
(L)
]·Cl·2H
O
, [Co
(L)
]·NO
·2.5H
O
, [Ni
(L)
]
, and [Zn
(L)
]
, have been designed and evaluated for their efficacy as antineoplastic agents. Among them, complex
exhibited higher anticancer efficacy than complexes
,
,
, and
platin against several cancer cell lines. Hemolysis assays revealed that complex
showed comparable hemolysis with
platin.
anticancer evaluations showed that complex
could retard tumor xenograft growth effectively with low systemic toxicity. Further studies revealed that complex
suppressed cancer cells by triggering multiple mechanisms involving the simultaneous inhibition of mitochondria and glycolytic bioenergetics. Overall, our study provides new insights into the anticancer mechanism of Co complexes, which can be used as a good strategy to overcome the flexibility of cancer cells to chemotherapy adaptation. |
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AbstractList | Non-platinum-metal complexes show great potential as anticancer agents. Herein, a series of dithiocarbazate non-Pt-metal complexes, including [Fe
(L)
]·Cl·2H
O
, [Co
(L)
]·NO
·2.5H
O
, [Ni
(L)
]
, and [Zn
(L)
]
, have been designed and evaluated for their efficacy as antineoplastic agents. Among them, complex
exhibited higher anticancer efficacy than complexes
,
,
, and
platin against several cancer cell lines. Hemolysis assays revealed that complex
showed comparable hemolysis with
platin.
anticancer evaluations showed that complex
could retard tumor xenograft growth effectively with low systemic toxicity. Further studies revealed that complex
suppressed cancer cells by triggering multiple mechanisms involving the simultaneous inhibition of mitochondria and glycolytic bioenergetics. Overall, our study provides new insights into the anticancer mechanism of Co complexes, which can be used as a good strategy to overcome the flexibility of cancer cells to chemotherapy adaptation. |
Author | Jiang, Hao Wen Deng, Jun Gang Huang, Guo Jin Gou, Yi Hou, Li Xia Jia, Xiaoying Yang, Feng |
Author_xml | – sequence: 1 givenname: Yi orcidid: 0000-0002-2900-4983 surname: Gou fullname: Gou, Yi organization: Laboratory of Respiratory Disease, Affiliated Hospital of Guilin Medical University, Guilin 541001, Guangxi, China – sequence: 2 givenname: Xiaoying surname: Jia fullname: Jia, Xiaoying organization: State Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences, Guangxi Norma University, Guilin 541004, Guangxi, China – sequence: 3 givenname: Li Xia surname: Hou fullname: Hou, Li Xia organization: Laboratory of Respiratory Disease, Affiliated Hospital of Guilin Medical University, Guilin 541001, Guangxi, China – sequence: 4 givenname: Jun Gang surname: Deng fullname: Deng, Jun Gang organization: Laboratory of Respiratory Disease, Affiliated Hospital of Guilin Medical University, Guilin 541001, Guangxi, China – sequence: 5 givenname: Guo Jin surname: Huang fullname: Huang, Guo Jin organization: Laboratory of Respiratory Disease, Affiliated Hospital of Guilin Medical University, Guilin 541001, Guangxi, China – sequence: 6 givenname: Hao Wen surname: Jiang fullname: Jiang, Hao Wen organization: State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China, Hangzhou Institute for Advanced Study, UCAS, Hangzhou 310000, China – sequence: 7 givenname: Feng orcidid: 0000-0002-4201-1416 surname: Yang fullname: Yang, Feng organization: Laboratory of Respiratory Disease, Affiliated Hospital of Guilin Medical University, Guilin 541001, Guangxi, China, State Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences, Guangxi Norma University, Guilin 541004, Guangxi, China |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35446587$$D View this record in MEDLINE/PubMed |
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Snippet | Non-platinum-metal complexes show great potential as anticancer agents. Herein, a series of dithiocarbazate non-Pt-metal complexes, including [Fe
(L)
]·Cl·2H
O... |
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Title | Dithiocarbazate–Fe III , −Co III , −Ni II , and −Zn II Complexes: Design, Synthesis, Structure, and Anticancer Evaluation |
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