• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[体外MTT法检测细胞毒性药物活性对宫颈癌化疗敏感性的预测价值]

[Predictive value of in vitro MTT assay chemosensitivity test of cytotoxic drug activity in cervical cancer].

作者信息

Xiao Yan, Li Jun-Dong, Shi Hong-Liu, Liu Ji-Hong, Feng Yan-Ling, Li Meng-Da

机构信息

State Key Laboratory of Oncology in South China, Guangzhou, Guangdong, 510060, PR China.

出版信息

Ai Zheng. 2007 Apr;26(4):386-9.

PMID:17430657
Abstract

BACKGROUND & OBJECTIVE: In recent years, the neoadjuvant chemotherapy for cervical cancer has evoked more and more attention and has been used widely. But the chemosensitivity of individuals to various antitumor drugs is different. This study was to investigate the chemosensitivity of cervical cancer cells to antitumor drugs using in vitro MTT assay chemosensitivity test.

METHODS

The sensitivity of fresh human cervical cancer cells from 32 patients to 9 cytotoxic drugs was tested using in vitro MTT assay.

RESULTS

The cytotoxic activities of the 9 drugs for cervical cancer were in sequence from high to low as follows: liposomal paclitaxel, taxol, carboplatin (CBP), ifosfamide (IFO), etoposide (VP-16), 5-fluorouracil (5-FU), cisplatin (DDP), bleomycin (BLM), and cyclophosphamide (CTX). Generally, cervical cancer cells were more sensitive to paclitaxel, taxol, and CBP than to other drugs (P<0.05) with inhibition rates of 56.56%, 55.66%, and 46.81%, respectively. Stage Ib1 cervical cancer cells were more sensitive to taxol, paclitaxel, and CBP than to other drugs with inhibition rates of 58.71%, 53.00%, and 49.25%, respectively; stage Ib2 cervical cancer cells were more sensitive to paclitaxel and taxol than to other drugs with inhibition rates of 65.26% and 50.06%. Both moderately and poorly differentiated squamous cell cancer cells were more sensitive to taxol, paclitaxel, and CBP than to other drugs with inhibition rates of 52.01%, 49.21%, and 40.02% for the former, and 60.02%, 61.16%, and 48.75% for the latter.

CONCLUSIONS

MTT assay, a sensitive and widely used chemosensitivity testing method, is helpful in sensitive drug screening and neoadjuvant chemotherapy regimen selection for cervical cancer. Cervical cancer cells are more sensitive to paclitaxel, taxol, and CBP than to other tested drugs in this study.

摘要

背景与目的

近年来,宫颈癌新辅助化疗越来越受到关注并得到广泛应用。但个体对各种抗肿瘤药物的化疗敏感性存在差异。本研究采用体外MTT法化疗敏感性试验,探讨宫颈癌细胞对抗肿瘤药物的化疗敏感性。

方法

采用体外MTT法检测32例患者新鲜宫颈癌细胞对9种细胞毒性药物的敏感性。

结果

9种药物对宫颈癌的细胞毒活性从高到低依次为:脂质体紫杉醇、紫杉醇、卡铂(CBP)、异环磷酰胺(IFO)、依托泊苷(VP-16)、5-氟尿嘧啶(5-FU)、顺铂(DDP)、博来霉素(BLM)和环磷酰胺(CTX)。总体而言,宫颈癌细胞对紫杉醇、脂质体紫杉醇和卡铂的敏感性高于其他药物(P<0.05),抑制率分别为56.56%、55.66%和46.81%。Ib1期宫颈癌细胞对紫杉醇、脂质体紫杉醇和卡铂的敏感性高于其他药物,抑制率分别为58.71%、53.00%和49.25%;Ib2期宫颈癌细胞对脂质体紫杉醇和紫杉醇的敏感性高于其他药物,抑制率分别为65.26%和50.06%。中、低分化鳞状细胞癌细胞对紫杉醇、脂质体紫杉醇和卡铂的敏感性均高于其他药物,前者的抑制率分别为52.01%、49.21%和40.02%,后者分别为60.02%、61.16%和48.75%。

结论

MTT法是一种敏感且广泛应用的化疗敏感性检测方法,有助于宫颈癌敏感药物筛选和新辅助化疗方案的选择。在本研究中,宫颈癌细胞对紫杉醇、脂质体紫杉醇和卡铂的敏感性高于其他受试药物。

相似文献

1
[Predictive value of in vitro MTT assay chemosensitivity test of cytotoxic drug activity in cervical cancer].[体外MTT法检测细胞毒性药物活性对宫颈癌化疗敏感性的预测价值]
Ai Zheng. 2007 Apr;26(4):386-9.
2
[Chemosensitivity testing of oral and maxillofacial cancer with biopsy specimens].[口腔颌面部癌活检标本的化学敏感性测试]
Zhonghua Kou Qiang Yi Xue Za Zhi. 2002 Nov;37(6):404-7.
3
Correlation of drug response with the ATP tumorchemosensitivity assay in primary FIGO stage III ovarian cancer.原发性国际妇产科联盟(FIGO)III期卵巢癌中药物反应与ATP肿瘤化疗敏感性检测的相关性
Gynecol Oncol. 2000 May;77(2):258-63. doi: 10.1006/gyno.2000.5728.
4
[Predicting clinical chemo-sensitivity of primary ovarian cancer using adenosine triphosphate-tumor chemosensitivity assay combined with detection of drug resistance genes].[应用三磷酸腺苷-肿瘤药敏试验联合耐药基因检测预测原发性卵巢癌临床化疗敏感性]
Zhonghua Fu Chan Ke Za Zhi. 2011 Mar;46(3):193-8.
5
[The evaluation of adenosine triphosphate bioluminescence assay for chemosensitivity testing of ovarian cancer cell line].[三磷酸腺苷生物发光法用于卵巢癌细胞系药敏试验的评估]
Zhonghua Fu Chan Ke Za Zhi. 1996 Feb;31(2):79-82.
6
[Relationship between the expression of P-glycoprotein, glutathione S-transferase-pi and thymidylate synthase proteins and adenosine triphosphate tumor chemosensitivity assay in cervical cancer].[宫颈癌中P-糖蛋白、谷胱甘肽S-转移酶π和胸苷酸合成酶蛋白表达与三磷酸腺苷肿瘤化疗药敏试验的关系]
Zhonghua Fu Chan Ke Za Zhi. 2007 Mar;42(3):201-5.
7
[Chemosensitivity test for 170 human breast carcinoma samples].[170例人乳腺癌样本的化学敏感性试验]
Hunan Yi Ke Da Xue Xue Bao. 1998;23(6):531-4.
8
Predictive value of the ATP chemosensitivity assay in epithelial ovarian cancer.ATP化学敏感性检测在上皮性卵巢癌中的预测价值。
Gynecol Oncol. 2001 Nov;83(2):334-42. doi: 10.1006/gyno.2001.6395.
9
[Anti-tumor effect of chemotherapeutic drugs on human gastric cancer cells in vitro and the relationship with Bcl-2 expression].化疗药物对人胃癌细胞的体外抗肿瘤作用及其与Bcl-2表达的关系
Zhonghua Wei Chang Wai Ke Za Zhi. 2008 May;11(3):276-9.
10
Inhibition of the mammalian target of rapamycin (mTOR) by rapamycin increases chemosensitivity of CaSki cells to paclitaxel.雷帕霉素对哺乳动物雷帕霉素靶蛋白(mTOR)的抑制作用可增强CaSki细胞对紫杉醇的化疗敏感性。
Eur J Cancer. 2006 May;42(7):934-47. doi: 10.1016/j.ejca.2005.12.018. Epub 2006 Mar 15.

引用本文的文献

1
Anti-Cancer Drug Sensitivity Assay with Quantitative Heterogeneity Testing Using Single-Cell Raman Spectroscopy.基于单细胞拉曼光谱的定量异质性检测用于抗癌药物药敏分析。
Molecules. 2018 Nov 7;23(11):2903. doi: 10.3390/molecules23112903.
2
PGPIPN, a therapeutic hexapeptide, suppressed human ovarian cancer growth by targeting BCL2.PGPIPN,一种治疗性六肽,通过靶向 BCL2 抑制人卵巢癌细胞生长。
PLoS One. 2013 Apr 8;8(4):e60701. doi: 10.1371/journal.pone.0060701. Print 2013.
3
Development of multicellular tumor spheroid (MCTS) culture from breast cancer cell and a high throughput screening method using the MTT assay.
从乳腺癌细胞中培养多细胞肿瘤球(MCTS)及其 MTT 检测法高通量筛选方法的建立。
PLoS One. 2012;7(9):e44640. doi: 10.1371/journal.pone.0044640. Epub 2012 Sep 6.