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The Blood Flow Shutdown Induced by Combretastatin A4 Impairs Gemcitabine Delivery in a Mouse Hepatocarcinoma
- Source :
- Frontiers in Pharmacology, Frontiers in Pharmacology, Vol. 7, p. 506 [1-8] (2016)
- Publication Year :
- 2016
- Publisher :
- Frontiers Media SA, 2016.
-
Abstract
- In recent clinical studies, vascular disrupting agents (VDAs) are mainly used in combination with chemotherapy. However, an often overlooked concern in treatment combination is the VDA-induced impairment of chemotherapy distribution in the tumor. The work presented here investigated the impact of blood flow shutdown induced by Combretastatin A4 (CA4) on gemcitabine uptake into mouse hepatocarcinoma. At 2 hours after CA4 treatment, using DCE-MRI, a significant decrease in the perfusion-relevant parameters Ktrans and Vp were observed in treated group compared with the control group. The blood flow shutdown was indeed confirmed by a histology study. In a third experiment, the total gemcitabine uptake was found to be significantly lower in treated tumors, as assessed in a separate experiment using ex vivo fluorine nuclear magnetic resonance spectroscopy. The amount of active metabolite gemcitabine triphosphate was also lower in treated tumors. In conclusion, the blood flow shutdown induced by VDAs can impact negatively on the delivery of small cytotoxic agents in tumors. The present study outlines the importance of monitoring the tumor vascular function when designing drug combinations.
- Subjects :
- 0301 basic medicine
Tumor perfusion
DCE-MRI
Shutdown
medicine.medical_treatment
Pharmacology
03 medical and health sciences
0302 clinical medicine
Vascular disrupting agent
tumor perfusion
medicine
Distribution (pharmacology)
19F NMR
Pharmacology (medical)
Active metabolite
Original Research
Chemotherapy
business.industry
Blood flow
Gemcitabine
030104 developmental biology
030220 oncology & carcinogenesis
Drug delivery
drug delivery
vascular disrupting agent
business
Ex vivo
medicine.drug
Subjects
Details
- ISSN :
- 16639812
- Volume :
- 7
- Database :
- OpenAIRE
- Journal :
- Frontiers in Pharmacology
- Accession number :
- edsair.doi.dedup.....b319f42ed7cf66fa72297d481bcb2dbb
- Full Text :
- https://doi.org/10.3389/fphar.2016.00506