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. 2010 Oct;119(1):140-5.
doi: 10.1016/j.ygyno.2010.06.024. Epub 2010 Jul 31.

Higher sensitivity to patupilone versus paclitaxel chemotherapy in primary uterine serous papillary carcinoma cell lines with high versus low HER-2/neu expression in vitro

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Higher sensitivity to patupilone versus paclitaxel chemotherapy in primary uterine serous papillary carcinoma cell lines with high versus low HER-2/neu expression in vitro

Daniel Paik et al. Gynecol Oncol. 2010 Oct.

Abstract

Objective: To compare the in vitro sensitivity/resistance to patupilone versus paclitaxel in uterine serous papillary carcinoma (USPC) with high versus low HER-2/neu expression.

Methods: Six primary USPC cell lines, half of which overexpress HER-2/neu at a 3+ level, were evaluated for growth rate and tested for their in vitro sensitivity/resistance to patupilone versus paclitaxel by MTS assays. Quantitative RT-PCR was used to identify potential mechanisms underlying the differential sensitivity/resistance to patupilone versus paclitaxel in primary USPC cell lines.

Results: Cell lines overexpressing HER-2/neu showed higher proliferation when compared to low HER-2/neu-expressing cell lines. Compared to low-expressing cell lines, high HER-2/neu expressors were significantly more sensitive to patupilone than to paclitaxel (P<0.0002). In contrast, there was no appreciable difference in sensitivity to patupilone versus paclitaxel in primary USPC cell lines with low HER-2/neu expression. Higher levels of β-tubulin III (TUBB3) and P-glycoprotein (ABCB1) were detected in USPC cell lines with high versus low HER-2/neu expression (P<0.05).

Conclusions: USPC overexpressing HER-2/neu display greater in vitro sensitivity to patupilone and higher levels of the patupilone molecular target TUBB3 when compared to low HER-2/neu expressors. Due to the adverse prognosis associated with HER-2/neu overexpression in USPC patients, patupilone may represent a promising novel drug to combine to platinum compounds in this subset of aggressive endometrial tumors.

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Figures

Figure 1
Figure 1. Growth curves of primary USPC cell lines
High HER-2/neu expressors (USPC-ARK-1, USPC-ARK-2, USPC-ARK-3) versus Low HER-2/neu expressors (USPC-ARK-4, USPC-ARK-5, USPC-ARK-6).
Figure 2
Figure 2. Representative dose-response curves following exposure to patupilone versus paclitaxel of USPC primary cell lines with High versus Low HER-2/neu expression
Survival was assessed by MTS assay as described in the Methods section. Each point on the cell line graph represents the mean of 3 estimations + SE.
Figure 3
Figure 3. IC50s of Patupilone and Paclitaxel in six USPC cell lines
Symbols (error bars) denote means (standard deviations) of IC50s. Text to the left of the symbols denotes the cell line, its paclitaxel/patupilone ratio of IC50s, and the ratio’s P value. Note that the individual ratios are significant (at P<0.05) for the cell lines that show HER-2/neu amplification by FISH, but not significant in the cell lines that don’t. As a class, the three HER-2/neuamplified lines taken together showed significantly lower IC50s for patupilone compared to paclitaxel (P=0.0002), whereas the three unamplified lines taken together did not (P=0.54).
Figure 4
Figure 4. P-glycoprotein (ABCB1) and β-tubulin class III (TUBB3) expression by RT-PCR in high versus low HER-2/neu expressor cell lines
Upper panel: ABCB1; Lower panel: TUBB3. Symbols (error bars) denote the geometric means (SDs) of relative expression in USPC-ARK-1 through ARK-6 ordered from left to right-respectively; symbol shapes and figure brackets denote groupings of cell lines into high and low HER-2/neu expressor groups as indicated by the legends. In each panel, the text between expressor groups reports the geometric mean fold change and P value between high and low expressor groups.

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