MLchartDataset catalogue

Albumin-binding Cisplatin Prodrug BTP-114

Term · Oncology and biomedicine · MLC-T-ONC-009753

A proprietary, albumin-binding platinum (Pt)-based complex containing a prodrug form of the platinum compound cisplatin and a maleimide moiety, with an ability to strongly and selectively bind human serum albumin (HSA), and with potential antineoplastic activity. Upon intravenous administration, the maleimide group of BTP-114 rapidly conjugates with HSA in the bloodstream; this prolongs the blood circulation, enhances the half-life, and alters the biodistribution of BTP-114, as compared to cisplatin alone. Thus, BTP-114 demonstrates enhanced extravasation to the tumor, an increased accumulation in the tumor tissue and enhanced uptake by cancer cells. The prodrug form is reduced in the hypoxic tumor cell environment, which releases the highly cytotoxic active metabolite cisplatin. Once inside the tumor cell, cisplatin binds to nucleophilic groups, such as GC-rich sites, in DNA and induces intrastrand and interstrand DNA cross-links, resulting in apoptosis and cell growth inhibition. Compared to cisplatin alone, BTP-114 has improved selectivity towards tumor tissue, thereby enhancing efficacy while reducing systemic toxicities.

Table 1. Record
IdentifierMLC-T-ONC-009753
FieldOncology and biomedicine
Synonymsalbumin-conjugating platinum-prodrug BTP-114; platinum-prodrug BTP-114; cisplatin prodrug BTP-114; cisplatin/maleimide-based complex BTP-114; prodrug BTP 114
ReferencesNational Cancer Institute Thesaurus (CC BY 4.0)
Record as JSON
{
  "id": "MLC-T-ONC-009753",
  "term": "Albumin-binding Cisplatin Prodrug BTP-114",
  "field": "Oncology and biomedicine",
  "definition": "A proprietary, albumin-binding platinum (Pt)-based complex containing a prodrug form of the platinum compound cisplatin and a maleimide moiety, with an ability to strongly and selectively bind human serum albumin (HSA), and with potential antineoplastic activity. Upon intravenous administration, the maleimide group of BTP-114 rapidly conjugates with HSA in the bloodstream; this prolongs the blood circulation, enhances the half-life, and alters the biodistribution of BTP-114, as compared to cisplatin alone. Thus, BTP-114 demonstrates enhanced extravasation to the tumor, an increased accumulation in the tumor tissue and enhanced uptake by cancer cells. The prodrug form is reduced in the hypoxic tumor cell environment, which releases the highly cytotoxic active metabolite cisplatin. Once inside the tumor cell, cisplatin binds to nucleophilic groups, such as GC-rich sites, in DNA and induces intrastrand and interstrand DNA cross-links, resulting in apoptosis and cell growth inhibition. Compared to cisplatin alone, BTP-114 has improved selectivity towards tumor tissue, thereby enhancing efficacy while reducing systemic toxicities.",
  "synonyms": [
    "albumin-conjugating platinum-prodrug BTP-114",
    "platinum-prodrug BTP-114",
    "cisplatin prodrug BTP-114",
    "cisplatin/maleimide-based complex BTP-114",
    "prodrug BTP 114"
  ],
  "references": [
    "National Cancer Institute Thesaurus"
  ],
  "url": "https://mlchart.com/terminology/oncology/albumin-binding-cisplatin-prodrug-btp-114/"
}

Record 599 of 17,721 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.