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Biological and Environmental Research Ontology
| Id | http://purl.obolibrary.org/obo/NCIT_C107387
http://purl.obolibrary.org/obo/NCIT_C107387
|
|---|---|
| Preferred Name | BP-Cx1-Platinum Complex BP-C1 |
| Definitions |
A combination agent composed of the benzo-poly-carbonic-acid polymer BP-Cx1 chelated to platinum with potential antineoplastic activity. Upon intramuscular injection, the polymer moiety of BP-Cx1-Platinum Complex BP-C1 (BP-C1) alters the permeability of the cell membranes, which allows for increased penetration of platinum into tumor cells. In turn, platinum binds to nucleophilic groups such as GC-rich sites in DNA and induces intrastrand and interstrand DNA cross-links, as well as DNA-protein cross-links. These cross-links result in apoptosis and cell growth inhibition. In addition, the BP-Cx1 ligand is able to stimulate the innate immune system and upregulates a variety of cytokines including interferon, tumor necrosis factor-alpha (TNF-alpha), granulocyte macrophage-colony stimulating factor (GM-CSF), and various interleukins (ILs) such as IL-6 and IL-25. In comparison to cisplatin and other platinum-based compounds, treatment with BP-C1 allows for less platinum administration, which reduces platinum-associated systemic toxicity and side effects, and enhances the safety profile while maintaining or improving its efficacy.
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | A combination agent composed of the benzo-poly-carbonic-acid polymer BP-Cx1 chelated to platinum with potential antineoplastic activity. Upon intramuscular injection, the polymer moiety of BP-Cx1-Platinum Complex BP-C1 (BP-C1) alters the permeability of the cell membranes, which allows for increased penetration of platinum into tumor cells. In turn, platinum binds to nucleophilic groups such as GC-rich sites in DNA and induces intrastrand and interstrand DNA cross-links, as well as DNA-protein cross-links. These cross-links result in apoptosis and cell growth inhibition. In addition, the BP-Cx1 ligand is able to stimulate the innate immune system and upregulates a variety of cytokines including interferon, tumor necrosis factor-alpha (TNF-alpha), granulocyte macrophage-colony stimulating factor (GM-CSF), and various interleukins (ILs) such as IL-6 and IL-25. In comparison to cisplatin and other platinum-based compounds, treatment with BP-C1 allows for less platinum administration, which reduces platinum-associated systemic toxicity and side effects, and enhances the safety profile while maintaining or improving its efficacy. |
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| label | BP-Cx1-Platinum Complex BP-C1
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| prefLabel | BP-Cx1-Platinum Complex BP-C1
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| in_subset | |
| Preferred_Name | BP-Cx1-Platinum Complex BP-C1
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| Is_Value_For_GDC_Property | |
| Maps_To | BP-Cx1-Platinum Complex BP-C1
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| PDQ_Open_Trial_Search_ID | 751002
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| prefixIRI | NCIT:C107387
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| NCI_Drug_Dictionary_ID | 751002
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| subClassOf | |
| code | C107387
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| type | |
| PDQ_Closed_Trial_Search_ID | 751002
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| Semantic_Type | Pharmacologic Substance
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| NCI_META_CUI | CL449598
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