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Published on: April 20, 2017
Modifications of cell-cycle induced by dpr, a new platinum-triamine complex containing procaine
M Viale1, G Melioli, W Pasquetti
1IST NAZL RIC CANC,SERV PATOL CLIN,I-16132 GENOA,ITALY. UNIV GENOA,IST ANAL & TECNOL FARMACEUT,I-16148 GENOA,ITALY.
cis-diamminechloro-[2-(diethylamino)ethyl 4-amino-benzoate, N4]-chlorideplatinum(II) monohydrochloride monohydrate (DPR) and cisplatin (cis-DDP) exhibit comparable cytotoxic activity and apoptosis induction in P388 leukemic cells. Both platinum compounds similarly affect cell cycle progression and programmed cell death.
Area of Science:
- Oncology
- Pharmacology
- Cell Biology
Background:
- Platinum-triamine complexes represent a novel class of anticancer agents.
- Procaine, a local anesthetic, is incorporated as a ligand in the novel platinum complex DPR.
- Understanding the cellular effects of novel platinum compounds is crucial for cancer therapy development.
Purpose of the Study:
- To compare the effects of DPR and cisplatin (cis-DDP) on P388 murine leukemic cells.
- To investigate the influence of these compounds on cell cycle phases and apoptosis induction.
- To evaluate the cytotoxic activity and DNA synthesis inhibition of DPR versus cis-DDP.
Main Methods:
- In vitro exposure of P388 leukemic cells to DPR and cis-DDP for 24 hours.
- Assessment of thymidine uptake to measure DNA synthesis inhibition.
- Trypan blue dye exclusion assay and flow cytometry to evaluate cytotoxicity and apoptosis.
Main Results:
- DPR and cis-DDP demonstrated comparable cytotoxic activity and inhibition of DNA synthesis.
- Both compounds induced similar modifications in cell cycle progression.
- Apoptosis was similarly induced by equivalent concentrations and exposure times of DPR and cis-DDP.
Conclusions:
- DPR exhibits comparable efficacy to cisplatin in P388 leukemic cells.
- The novel platinum-triamine complex DPR shows similar effects on cell cycle and apoptosis as cis-DDP.
- DPR represents a potential candidate for further investigation in cancer treatment.
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