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Cytotoxic potentiation of vinblastine and paclitaxel by L-canavanine in human cervical cancer and hepatocellular carcinoma cells (article of Phytomedicine Vol.22 Iss.14, Dec 2015, p.1232-1237
Bibliografi
Author:
Nurcahyanti, Agustina Dwi Retno
;
Wink, Michael
Topik:
L-canavanine
;
Vinblastine
;
Paclitaxel
;
Microtubule
;
Argininosuccinate synthase
;
Synergy
;
JABFUNG-FKIK-ADRN-2022-01
Bahasa:
(EN )
Penerbit:
Elsevier
Tahun Terbit:
2015
Jenis:
Article - diterbitkan di jurnal ilmiah internasional
Fulltext:
B1 Publikasi Rev Bu Agustin.pdf
(4.07MB;
3 download
)
Abstract
Background
The non-protein amino acid L-canavanine (L-CAV), found in several plants of the family Fabaceae is an antimetabolite which shows anticancer activity due to its ability to be incorporated into protein in the place of its analogue, L-arginine (L-ARG), leading to the alteration of the 3D conformation of newly synthesised proteins and usually a loss of their function.
Purpose
In this study, the ability of L-CAV to potentiate the cytotoxicity of microtubule- targeting drugs used in the chemotherapy of cancer, vinblastine (VIN) and paclitaxel (PTX) was evaluated.
Material and methods
The following cancer cells grown in arginine-rich and arginine-free media were employed: HeLa, Hep G2 and SK-HEP-1. Drug combination experiment used a method based on the median-effect principle and mass-action law.
Results
We observed that L-CAV, which is hardly toxic alone, potentiated the cytotoxicity of VIN and PTX in HeLa and hepatocellular carcinoma cells.
Conclusion
This is the first study showing the cytotoxic potentiation of microtubule-targeting drugs by L-CAV. The mechanism of synergy and animal studies need to be investigated further to see whether L-CAV might become an adjuvant in cancer treatment.
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