Drug intelligence / Profile preview

bortezomib + oxaliplatin

Development stage
Unknown
Lead developer
Millennium Pharmaceuticals
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Intravenous, Subcutaneous
01

Overview

Bortezomib + oxaliplatin is an investigational combination therapy consisting of two small molecule chemotherapeutic agents: bortezomib, a reversible proteasome inhibitor, and oxaliplatin, a platinum-based DNA crosslinking agent. Bortezomib inhibits the 26S proteasome, disrupting protein degradation and leading to cell cycle arrest and apoptosis in cancer cells. Oxaliplatin forms DNA adducts that inhibit DNA replication and transcription, resulting in cytotoxicity. The rationale for combining these drugs is based on potential synergy—bortezomib may enhance the effects of platinum-induced DNA damage by interfering with cellular repair mechanisms. This combination has been studied primarily in patients with advanced solid tumors (including colorectal cancer) to assess safety, tolerability (notably neurotoxicity), pharmacokinetics, and preliminary efficacy[1][2][3].

02

Targets

DNAPSMB5 (Proteasome subunit beta Type-5)PSMB7 (Proteasome subunit beta type-7)

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