Differential in vitro sensitivity to patupilone versus paclitaxel in uterine and ovarian carcinosarcoma cell lines is linked to tubulin-beta-III expression

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• 作者：Luisa Carrara^b ; Federica Guzzo^c ; Dana M. Roque^a ; Stefania Bellone^a ; Cocco Emiliano^a ; Enrico Sartori^b ; Sergio Pecorelli^b ; Peter E. Schwartz^a ; Thomas J. Rutherford^a ; Alessandro D. Santin^a ; ^{alessandro.santin@yale.edu}
• 关键词：Endometrial neoplasms ; Uterine serous tumors ; HER-2/neu ; Patupilone ; Paclitaxel
• 刊名：Gynecologic Oncology
• 出版年：2012
• 期刊代码：295_00908258
• 类别：med
• 出版时间：April, 2012
• 卷：125
• 期：1
• 页码：231-236
• 文件大小：418 K

摘要

Objective

To compare the in vitro sensitivity/resistance to patupilone versus paclitaxel in uterine and ovarian carcinosarcomas (CS).

Methods

Five primary carcinosarcoma cell lines, two from uterine and three of ovarian origin, were evaluated for growth rate and tested for their in vitro sensitivity/resistance to patupilone versus paclitaxel by MTS assays. To identify potential mechanisms underlying the differential sensitivity/resistance to patupilone, expression levels of 尾-tubulin III (TUBB3) were determined with quantitative-real-time-polymerase-chain-reaction (q-RT-PCR) in primary uterine and ovarian CS cell lines and in 26 uterine and 9 ovarian CS fresh-frozen-tissues.

Results

No appreciable difference in sensitivity to patupilone versus paclitaxel was noted in ovarian CS cell lines, or when uterine and ovarian CS cell lines were compared in their response to paclitaxel. In contrast, uterine CS cell lines were found to be significantly more sensitive to patupilone than to paclitaxel (P < 0.002) and demostrated lower IC_50s to patupilone (range 0.76-0.93 nM) when compared to ovarian CS (range 1.9-3.4 nM, p < 0.05). Higher levels of TUBB3 were detected in uterine CS cell lines and fresh frozen tissues when compared to ovarian CS (P < 0.05).

Conclusions

Uterine CS cell lines are significantly more sensitive than ovarian CS cell lines to patupilone versus paclitaxel. High expression of TUBB3 is associated with sensitivity to patupilone in primary CS cell lines and may act as a genetic marker to predict chemotherapy efficacy. Patupilone may represent a promising drug in the treatment of this subset of rare but highly aggressive gynecological tumors.