乳腺癌分子亚型与体外三磷酸腺苷化学敏感性试验的相关性。

Journal of the Korean Surgical Society Pub Date : 2013-06-01 Epub Date: 2013-05-28 DOI:10.4174/jkss.2013.84.6.313
Jina Chang, Anbok Lee, Jihyun Lee, Woosung Lim, Sun Hee Sung, Byung-In Moon
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引用次数: 6

摘要

目的:一种化疗方案的经验性使用在个体乳腺癌患者的治疗中显示出不同的结果。最近的研究显示了基于三磷酸腺苷的化疗反应测定(ATP-CRA)的有效性。然而,人们对化疗敏感性与乳腺癌分子亚型之间的关系知之甚少。因此,我们研究了ATP-CRA的结果是否与乳腺癌的分子亚型相关。方法:2007年9月至2010年12月在梨花女子大学木洞医院接受ATP-CRA治疗的287例乳腺癌患者入组研究。分析患者的激素受体状态、HER2/neu表达及化疗敏感性试验结果。结果:在所有四种亚型中,两种药物联合使用的平均细胞死亡率明显高于单一药物。在本研究的乳腺癌细胞系中,每位患者的化疗敏感性反应范围非常广泛且各不相同。因此,乳腺癌的分子亚型在选择有效的化疗药物方面尚无定论,而在治疗前进行体外化疗敏感性试验可能是为每位患者制定化疗计划的有用方法。结论:乳腺癌患者对抗癌药物的化疗敏感性存在个体差异。乳腺癌的分子亚型对选择有效的化疗药物尚无定论,治疗前的体外化疗敏感性试验可能对每位患者的化疗计划更有帮助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Correlation between the molecular subtype of breast cancer and the in vitro adenosine triphosphate-based chemosensitivity assay.

Correlation between the molecular subtype of breast cancer and the in vitro adenosine triphosphate-based chemosensitivity assay.

Correlation between the molecular subtype of breast cancer and the in vitro adenosine triphosphate-based chemosensitivity assay.

Correlation between the molecular subtype of breast cancer and the in vitro adenosine triphosphate-based chemosensitivity assay.

Purpose: The empirical use of a chemotherapy regimen shows different results in individual breast cancer patient treatment. Recent studies showed the effectiveness of the adenosine triphosphate-based chemotherapy response assay (ATP-CRA). However, little is known about the correlation between chemosensitivity and breast cancer molecular subtypes. Therefore, we investigated whether the result of ATP-CRA is associated with a molecular subtype of breast cancer.

Methods: Two hundred eighty-seven patients diagnosed with breast cancer and receiving ATP-CRA at Mokdong Hospital, Ewha Womans University between September 2007 and December 2010 were enrolled in this study. Hormone receptor status, HER2/neu expression, and results of chemosensitivity tests of the patients was analyzed.

Results: In all of four subtypes, the combination of two agents showed significant higher mean cell death rate than a single agent. Within the breast cancer cell lines in this study, the range of chemosensitivity response was very wide and varied for each patient. For this reason, the molecular subtype of breast cancer is inconclusive in choosing an effective chemotherapeutic agent and in vitro chemosensitivity test, prior to therapy, could be a useful method for planning chemotherapy for each patient.

Conclusion: Chemosensitivity response to anticancer agents was found to vary depending on the individual breast cancer patients. The molecular subtype of breast cancer is inconclusive to choose the effective chemotherapeutic agent and the in vitro chemosensitivity test, prior to therapy, could be more useful for planning chemotherapy for each patient.

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