High expression of crystallin ?B represents an independent molecular marker for unfavourable ovarian cancer patient outcome and impairs TRAIL- and cisplatin-induced apoptosis in human ovarian cancer cells.

Volkmann, J; Reuning, U; Rudelius, M; Häfner, N; Schuster, T; Rose, AB; Weimer, J; Hilpert, F; Kiechle, M; Dürst, M; Arnold, N; Schmalfeldt, B; Meindl, A; Ramser, J

doi:10.1002/ijc.27975

User: Guest

Institut für Medizinische Statistik und Epidemiologie

Back
Back to start of result list
Permanent link for displayed object

Title:: High expression of crystallin ?B represents an independent molecular marker for unfavourable ovarian cancer patient outcome and impairs TRAIL- and cisplatin-induced apoptosis in human ovarian cancer cells.
Document type:: Journal Article
Author(s):: Volkmann, J; Reuning, U; Rudelius, M; Häfner, N; Schuster, T; Rose, AB; Weimer, J; Hilpert, F; Kiechle, M; Dürst, M; Arnold, N; Schmalfeldt, B; Meindl, A; Ramser, J
Abstract:: Dysregulated apoptotic pathways are regarded as major reasons for chemoresistance development as a particular challenge in ovarian cancer therapy. In search of molecular factors affecting human ovarian cancer cell apoptosis and, consequently, patient survival, we examined tumors of 103 platinum-/taxane-treated ovarian cancer patients by mRNA-array hybridization, qPCR, and immunohistochemistry. We identified high expression of crystallin ?B (CRYAB), a proposed negative regulator of tumor necrosis factor-related apoptosis inducing ligand (TRAIL)-mediated apoptosis. By Kaplan Meier analysis, this factor turned out to be significantly associated with poor patient outcome [overall survival (OS) p = 0.001, recurrence-free survival (RFS) p = 0.003]. Elevated hazard ratios (HR) were estimated with regard to OS (HR = 2.11, 95% CI 1.10-4.06) and RFS (HR = 1.92, 95% CI 1.07-3.47) in multivariable analyses. These associations were confirmed in independent, publicly available mRNA data comprising 431 patients for OS (p < 0.001) and 413 for RFS (p < 0.001). Our findings were validated by studying apoptotic events in cultured human ovarian cancer cells which were stably transfected to express elevated CRYAB levels. These data emphasized the crucial role of CRYAB in human ovarian cancer biology since TRAIL- as well as cisplatin-induced apoptosis was significantly impaired as a function of enhanced CRYAB expression. Taken together, we identified CRYAB as an independent biomarker for unfavourable outcome of human ovarian cancer patients. Since TRAIL is currently tested as anti-cancer drug and large proportions of the present patient cohort displayed low CRYAB levels in their tumors, CRYAB may enable the selection of patient subgroups benefiting most from TRAIL-containing therapy.
Journal title abbreviation:: Int J Cancer
Year:: 2013
Journal volume:: 132
Journal issue:: 12
Pages contribution:: 2820-32
Language:: eng
Fulltext / DOI:: doi:10.1002/ijc.27975
Pubmed ID:: http://view.ncbi.nlm.nih.gov/pubmed/23225306
Print-ISSN:: 0020-7136
TUM Institution:: Frauenklinik und Poliklinik; Institut für Medizinische Statistik und Epidemiologie
BibTeX