Class III β-tubulin is a marker of paclitaxel resistance in carcinomas of unknown primary site

被引:59
作者
Seve, Pascal [1 ]
Reiman, Tony
Lai, Raymond
Hanson, John
Santos, Cheryl
Johnson, Lorelei
Dabbagh, Laith
Sawyer, Michael
Dumontet, Charles
Mackey, John R.
机构
[1] Hospices Civils Lyon, Hotel Dieu, Dept Internal Med, F-69288 Lyon 02, France
[2] Univ Alberta, Dept Oncol, Edmonton, AB T6G 1Z2, Canada
[3] Univ Alberta, Dept Pathol, Edmonton, AB T6G 1Z2, Canada
[4] Hop Edouard Herriot, Lab Immunol Hemopathies, F-69437 Lyon, France
关键词
cancer of unknown primary; chemoresistance; paclitaxel; tubulin; tubulin III;
D O I
10.1007/s00280-006-0343-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose In this study, we determine the prevalence and the prognostic value of the class III beta-tubulin microtubule protein examined immunohistochemically, in tumors of 40 patients with carcinomas of unknown primary site treated with paclitaxel-based chemotherapy. Methods Immunohistochemical intensity of staining and percentage of cells were quantified. Clinical characteristics, response to chemotherapy, progression-free survival, and overall survival were assessed for relationships with the expression of class III beta-tubulin. Results The response rate was 17.9% (seven partial responses among 39 valuable patients), while eleven patients had a stable disease (28.2%) and 21 patients progressed on therapy (53.8%). Patients with high class III beta-tubulin expression were more resistant to taxane-based chemotherapy, defined as progression under treatment, while patient characteristics were not found to be correlated with response to chemotherapy. Patients whose tumors expressed high levels of class III beta-tubulin isotype had shorter overall survival, while there was a trend for an association with progression free survival. Multivariate analysis showed that class III beta-tubulin expression was independently correlated with progression free survival and overall survival. Conclusions These findings suggest that a high level of expression of class III beta-tubulin in tumor cells is associated with resistance to paclitaxel and decreased survival in patients with carcinomas of unknown primary receiving paclitaxel-based chemotherapy.
引用
收藏
页码:27 / 34
页数:8
相关论文
共 32 条
[1]  
BANERJEE A, 1990, J BIOL CHEM, V265, P1794
[2]   Cancer of unknown primary:: clinicopathologic correlations [J].
Blaszyk, H ;
Hartmann, A ;
Björnsson, J .
APMIS, 2003, 111 (12) :1089-1094
[3]   Carboplatin plus paclitaxel in unknown primary carcinoma: A phase II Hellenic Cooperative Oncology Group study [J].
Briasoulis, E ;
Kalofonos, H ;
Bafaloukos, D ;
Samantas, E ;
Fountzilas, G ;
Xiros, N ;
Skarlos, D ;
Christodoulou, C ;
Kosmidis, F ;
Pavlidis, N .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (17) :3101-3107
[4]   Summary of the Standards, Options and Recommendations for the management of patients with carcinoma of unknown primary site (2002) [J].
Bugat, R ;
Bataillard, A ;
Lesimple, T ;
Voigt, JJ ;
Culine, S ;
Lortholary, A ;
Merrouche, Y ;
Ganem, G ;
Kaminsky, MC ;
Negrier, S ;
Perol, M ;
Laforêt, C ;
Bedossa, P ;
Bertrand, G ;
Coindre, JM ;
Fizazi, K .
BRITISH JOURNAL OF CANCER, 2003, 89 (Suppl 1) :S59-S66
[5]  
BURKHART CA, 2001, BIOCHIM BIOPHYS ACTA, V1471, P1
[6]   Development and validation of a prognostic model to predict the length of survival in patients with carcinomas of an unknown primary site [J].
Culine, S ;
Kramar, A ;
Saghatchian, M ;
Bugat, R ;
Lesimple, T ;
Lortholary, A ;
Merrouche, Y ;
Laplanche, A ;
Fizazi, K .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (24) :4679-4683
[7]   Taxol differentially modulates the dynamics of microtubules assembled from unfractionated and purified beta-tubulin isotypes [J].
Derry, WB ;
Wilson, L ;
Khan, IA ;
Luduena, RF ;
Jordan, MA .
BIOCHEMISTRY, 1997, 36 (12) :3554-3562
[8]   Mechanisms of action of and resistance to antitubulin agents: Microtubule dynamics, drug transport, and cell death [J].
Dumontet, C ;
Sikic, BI .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (03) :1061-1070
[9]   Class III β-tubulin overexpression is a marker of poor clinical outcome in advanced ovarian cancer patients [J].
Ferrandina, G ;
Zannoni, GF ;
Martinelli, E ;
Paglia, A ;
Gallotta, V ;
Mozzetti, S ;
Scambia, G ;
Ferlini, C .
CLINICAL CANCER RESEARCH, 2006, 12 (09) :2774-2779
[10]   Paclitaxel-resistant human ovarian cancer cells have mutant beta-tubulins that exhibit impaired paclitaxel-driven polymerization [J].
Giannakakou, P ;
Sackett, DL ;
Kang, YK ;
Zhan, ZR ;
Buters, JTM ;
Fojo, T ;
Poruchynsky, MS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (27) :17118-17125