Drug intelligence / Profile preview

cisplatin + etoposide + interferon gamma

Development stage
Unknown
Lead developer
Michigan State University
Modality
Recombinant Proteins and Enzymes, Small Molecules
Administration
Intravenous, Subcutaneous
01

Overview

This is a combination regimen consisting of three agents: - **Cisplatin** is a platinum-based chemotherapeutic classified as an alkylating agent. It exerts its antineoplastic effects by cross-linking DNA, thereby inhibiting DNA replication and transcription, leading to cell death. Cisplatin is cell cycle-nonspecific and disrupts DNA function through multiple mechanisms including direct cross-linking of guanine bases[5]. - **Etoposide** is an epipodophyllotoxin derivative that inhibits the enzyme DNA topoisomerase II, resulting in double-strand breaks in DNA and inhibition of cell division. Etoposide acts primarily during the S and G2 phases of the cell cycle[7]. - **Interferon gamma (IFN-γ)** is a type II interferon cytokine with immunomodulatory, antiproliferative, pro-apoptotic, antiangiogenic, and antitumor properties. It enhances antigen presentation on tumor cells via upregulation of MHC molecules and stimulates immune effector functions such as cytotoxic T lymphocyte activity[6][8][9]. This combination has been investigated in clinical trials for cancer therapy—most notably for non-small cell lung cancer—where IFN-gamma was used as an immunomodulatory adjunct to standard chemotherapy with cisplatin and etoposide[1][4]. The rationale was to enhance antitumor immunity alongside direct cytotoxic effects.

Other names
cisplatin and etoposide with interferon gammacisplatin plus etoposide plus IFN-gamma
02

Targets

TOP2A (DNA topoisomerase II)DNAIFNGR1 (Interferon gamma receptor 1)

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