Modulation of septin and molecular motor recruitment in the microtubule environment of the Taxol-resistant human breast cancer cell line MDA-MB-231

被引:32
作者
Froidevaux-Klipfel, Laurence [1 ]
Poirier, Florence
Boursier, Celine
Crepin, Ronan [1 ]
Poues, Christian [1 ,2 ]
Baudin, Bruno [1 ,3 ]
Baillet, Anita [1 ]
机构
[1] Univ Paris 11, EA4530, IFR IPSIT 141, Fac Pharm, F-92296 Chatenay Malabry, France
[2] Hop Antoine Beclere, AP HP, Lab Biochim Hormonol, Clamart, France
[3] Hop Saint Antoine, AP HP, Biochim A, Paris, France
关键词
Cell biology; Dynein; Kinesin; Microtubule; Septin; Taxol resistance; BETA-TUBULIN ISOTYPES; HEAT-SHOCK-PROTEIN; MAMMALIAN SEPTIN; PACLITAXEL TAXOL; DRUG-RESISTANCE; EXPRESSION; PROTEOMICS; KINESIN; CHEMORESISTANCE; CYTOKINESIS;
D O I
10.1002/pmic.201000789
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Cell resistance to low doses of paclitaxel (Taxol) involves a modulation of microtubule (MT) dynamics. We applied a proteomic approach based on 2-DE coupled with MS to identify changes in the MT environment of Taxol-resistant breast cancer cells. Having established a proteomic pattern of the microtubular proteins extracted from MDA-MB-231 cells, we verified by Western blotting that in resistant cells, alpha- and beta-tubulins (more specifically the beta III and beta IV isotypes) increased. Interestingly, four septins (SEPT2, 8, 9 and 11), which are GTPases involved in cytokinesis and in MT/actin cytoskeleton organization, were overexpressed and enriched in the MT environment of Taxol-resistant cells compared to their sensitive counterpart. Changes in the MT proteome of resistant cells also comprised increased kinesin-1 heavy chain expression and recruitment on MTs while dynein light chain-1 was down-regulated. Modulation of motor protein recruitment around MTs might reflect their important role in controlling MT dynamics via the organization of signaling pathways. The identification of proteins previously unknown to be linked to taxane-resistance could also be valuable to identify new biological markers of resistance.
引用
收藏
页码:3877 / 3886
页数:10
相关论文
共 66 条
[1]
Alli E, 2002, CANCER RES, V62, P6864
[2]
SEPT9_V1 protein expression is associated with human cancer cell resistance to microtubule disrupting agents [J].
Arnir, Sharon ;
Mabjeesh, Nicola J. .
CANCER BIOLOGY & THERAPY, 2007, 6 (12) :1926-1931
[3]
Microtubule stabilizing agents: Their molecular signaling consequences and the potential for enhancement by drug combination [J].
Bergstralh, Daniel T. ;
Ting, Jenny P. -Y. .
CANCER TREATMENT REVIEWS, 2006, 32 (03) :166-179
[4]
Do β-tubulin mutations have a role in resistance to chemotherapy? [J].
Berrieman, HK ;
Lind, MJ ;
Cawkwell, L .
LANCET ONCOLOGY, 2004, 5 (03) :158-164
[5]
Investigation of doxorubicin resistance in MCF-7 breast cancer cells using shot-gun comparative proteomics with proteolytic 18O labeling [J].
Brown, KJ ;
Fenselau, C .
JOURNAL OF PROTEOME RESEARCH, 2004, 3 (03) :455-462
[6]
Phylogenetic and evolutionary analysis of the septin protein family in metazoan [J].
Cao, Lihuan ;
Ding, Xiangming ;
Yu, Wenbo ;
Yang, Xianmei ;
Shen, Suqin ;
Yu, Long .
FEBS LETTERS, 2007, 581 (28) :5526-5532
[7]
Chuthapisith S, 2007, INT J ONCOL, V30, P1545
[8]
Crossett Ben, 2008, V141, P271
[9]
Kinesin-1 Regulates Microtubule Dynamics via a c-Jun N-terminal Kinase-dependent Mechanism [J].
Daire, Vanessa ;
Giustiniani, Julien ;
Leroy-Gori, Ingrid ;
Quesnoit, Melanie ;
Drevensek, Stephanie ;
Dimitrov, Ariane ;
Perez, Franck ;
Poues, Christian .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (46) :31992-32001
[10]
Overexpression of Kinesins Mediates Docetaxel Resistance in Breast Cancer Cells [J].
De, Sarmishtha ;
Cipriano, Rocky ;
Jackson, Mark W. ;
Stark, George R. .
CANCER RESEARCH, 2009, 69 (20) :8035-8042