Arsenic trioxide induces depolymerization of microtubules in an acute promyelocytic leukemia cell line.
10.5045/kjh.2012.47.2.105
- Author:
Jin Ho BAEK
1
;
Chang Hoon MOON
;
Seung Joo CHA
;
Hee Soon LEE
;
Eui Kyu NOH
;
Hawk KIM
;
Jong Ho WON
;
Young Joo MIN
Author Information
1. Division of Hematology and Oncology, Department of Internal Medicine, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea. yjmin@uuh.ulsan.kr
- Publication Type:Original Article
- Keywords:
Acute promyelocytic leukemia;
Arsenic trioxide;
Tubulin;
Apoptosis;
Antimitotic agents
- MeSH:
Antimitotic Agents;
Apoptosis;
Arsenic;
Arsenicals;
Cell Line;
Fluorescence;
Humans;
Immunohistochemistry;
Leukemia, Promyelocytic, Acute;
Microtubules;
Oxides;
Paclitaxel;
Polymerization;
Polymers;
Protein Processing, Post-Translational;
Tubulin;
Vincristine
- From:Korean Journal of Hematology
2012;47(2):105-112
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: Arsenic trioxide (As2O3) is a well-known and effective treatment that can result in clinical remission for patients diagnosed with acute promyelocytic leukemia (APL). The biologic efficacy of As2O3 in APL and solid tumor cells has been explained through its actions on anti-proliferation, anti-angiogenesis, and apoptotic signaling pathways. We theorize that As2O3 activates a pathway that disrupts microtubule dynamics forming abnormal, nonfunctioning mitotic spindles, thus preventing cellular division. In this study, we investigated how As2O3 induces apoptosis by causing microtubule dysfunction. METHODS: Cultured NB4 cells were treated with As2O3, paclitaxel, and vincristine. Flow cytometric analysis was then performed. An MTT assay was used to determine drug-mediated cytotoxicity. For tubulin polymerization assay, each polymerized or soluble tubulin was measured. Microtubule assembly-disassembly was measured using a tubulin polymerization kit. Cellular microtubules were also observed with fluorescence microscopy. RESULTS: As2O3 treatment disrupted tubulin assembly resulting in dysfunctional microtubules that cause death in APL cells. As2O3 markedly enhanced the amount of depolymerized microtubules. The number of microtubule posttranslational modifications on an individual tubulin decreased with As2O3 concentration. Immunocytochemistry revealed changes in the cellular microtubule network and formation of polymerized microtubules in As2O3-treated cells. CONCLUSION: The microtubules alterations found with As2O3 treatment suggest that As2O3 increases the depolymerized forms of tubulin in cells and that this is potentially due to arsenite's negative effects on spindle dynamics.
