通过比较分析细胞活力和胸腺苷酸合成酶mRNA表达来评估结直肠癌细胞系化疗敏感性的实用方法。

Journal of the Korean Surgical Society Pub Date : 2012-01-01 Epub Date: 2011-12-27 DOI:10.4174/jkss.2012.82.1.28
Hyun Yong Hwang
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引用次数: 0

摘要

目的:本研究的目的是提出在实践中进行的化学敏感性试验中可能存在的问题,并推测更准确的化学敏感性评估的可行措施。方法:用5-氟尿嘧啶(5-FU)治疗3例结直肠癌细胞(RSC、RRC1和RRC2)。在替换70%培养基的第2天、第5天、第7天、第3天分别检测肿瘤细胞的抑制率(%)和胸腺苷酸合成酶(TS) mRNA的相对定量。计算产生50%抑制(Dm)的剂量以评估药物效果。分析TS mRNA的相对定量以及TS mRNA水平与5-FU浓度的相关性。结果:第7天RRC1的耐药程度高于RRC2,但更换介质后第3天RRC2的Dm值从12.3上升至18.1。D2和D7上RSC的TS mRNA平均水平分别显著低于RRC1和RRC2 (P = 0.004, D2 = 0.004;P = 0.010, P = 0.006 (D7)。第2天,RRC1中TS mRNA水平与5-FU浓度呈显著负相关(相关系数= -0.867,P = 0.015)。另一方面,RRC2的相关性不显著(r = 0.067)。结论:在化疗敏感性试验中评价某一点对癌细胞的抑制作用似乎不足以确定化疗方案。为了化学敏感性测试的实际应用,需要实施多边方法,例如评估介质替换前后癌细胞存活的试验以及TS mRNA水平与5-FU浓度之间的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A practical approach for assessing chemosensitivity in colorectal cancer cell lines by comparative analysis of cell viability and thymidylate synthase mRNA expression.

Purpose: The purpose of this study is to suggest a probable problem in chemosensitivity tests performed in practice and to speculate on practicable measures for more accurate chemosensitivity evaluation.

Methods: Three colorectal cancer cells (RSC, RRC1, and RRC2) were treated with 5-fluorouracil (5-FU). Inhibition percentage (%inhibition) of cancer cells and relative quantitation of thymidylate synthase (TS) mRNA were measured on day 2, day 5 after replacement of 70% media on day 2, day 7, and day 3 after replacement of all media on day 7. Doses that produced 50% inhibition (Dm) were calculated to evaluate drug effect. Relative quantitation of TS mRNA and correlations between TS mRNA levels and 5-FU concentrations were analyzed.

Results: RRC1 was more resistant than RRC2 on day 7, but Dm value of RRC2 increased three days after replacement of media from 12.3 to 18.1. Mean TS mRNA levels of RSC on D2 and D7 were significantly lower than those of RRC1 and RRC2, respectively (P = 0.004, P = 0.004 on D2; P = 0.010, P = 0.006 on D7). TS mRNA levels in RRC1 were significantly reversely correlated with 5-FU concentrations on day 2 (correlation coefficient = -0.867, P = 0.015). On the other hand, correlations were not significant in RRC2 (r = 0.067).

Conclusion: Evaluating %inhibition of cancer cells at one point in chemosensitivity tests seems to be inadequate in determining chemotherapeutic regimens. Multilateral approaches, such as trials evaluating cancer cell survival before and after media replacement and correlations between TS mRNA levels and 5-FU concentrations, needs to be implemented for the practical application of chemosensitivity tests.

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