• 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

低分化人胃癌比高分化癌对抗肿瘤药物更敏感。

Poorly differentiated human gastric carcinoma is more sensitive to antitumor drugs than is well differentiated carcinoma.

作者信息

Maehara Y, Anai H, Kusumoto H, Sugimachi K

出版信息

Eur J Surg Oncol. 1987 Jun;13(3):203-6.

PMID:3036603
Abstract

The chemosensitivities of 41 poorly differentiated gastric cancer tissues were compared with that of 16 well differentiated tissues, using the in vitro succinate dehydrogenase inhibition test. These human tissues obtained at the time of surgery were exposed to six different antitumor drugs: carboquone (CQ), adriamycin (ADM), mitomycin C (MMC), aclacinomycin A (ACR), cisplatin (DDP) and 5-fluorouracil (5-FU). The chemosensitivity was determined as positive when the succinate dehydrogenase (SD) activity of the drug exposed cells was decreased to below 50% of that of control cells, on day 3 of exposure. Decrease in SD activity was remarkable in the poorly differentiated tissues, compared to the well differentiated tissues, exposed to ADM, MMC, DDP and 5-FU. The sensitive rates were higher in the poorly differentiated tissues than in the well differentiated tissues, against all six antitumor drugs. Sixty-three per cent of the poorly differentiated tissues were sensitive to more than three antitumor drugs, in an identical tissue, but the rate was only 19% in the well differentiated tissues. The resistant rates to all drugs tested were 20% in the poorly differentiated and 31% in the well differentiated tissues. This would indicate that patients with a poorly differentiated gastric cancer will probably show a better response to antitumor drugs, compared to those with a well differentiated type.

摘要

采用体外琥珀酸脱氢酶抑制试验,比较了41例低分化胃癌组织与16例高分化组织的化学敏感性。这些手术时获取的人体组织被暴露于六种不同的抗肿瘤药物:卡波醌(CQ)、阿霉素(ADM)、丝裂霉素C(MMC)、阿克拉霉素A(ACR)、顺铂(DDP)和5-氟尿嘧啶(5-FU)。当暴露于药物的细胞的琥珀酸脱氢酶(SD)活性在暴露第3天时降至对照细胞活性的50%以下时,化学敏感性被判定为阳性。与高分化组织相比,暴露于ADM、MMC、DDP和5-FU的低分化组织中SD活性的降低更为显著。在所有六种抗肿瘤药物方面,低分化组织的敏感率高于高分化组织。63%的低分化组织对同一组织中的三种以上抗肿瘤药物敏感,但高分化组织中的这一比例仅为19%。低分化组织对所有测试药物的耐药率为20%,高分化组织为31%。这表明,与高分化型胃癌患者相比,低分化胃癌患者可能对抗肿瘤药物表现出更好的反应。

相似文献

1
Poorly differentiated human gastric carcinoma is more sensitive to antitumor drugs than is well differentiated carcinoma.低分化人胃癌比高分化癌对抗肿瘤药物更敏感。
Eur J Surg Oncol. 1987 Jun;13(3):203-6.
2
Resistance to anticancer drugs of well differentiated gastric adenocarcinoma with venous invasion.伴静脉侵犯的高分化胃腺癌对抗癌药物的耐药性
Eur J Surg Oncol. 1992 Apr;18(2):142-5.
3
Lung adenocarcinoma is more sensitive than gastric adenocarcinoma to anticancer drugs in vitro.在体外,肺腺癌比胃腺癌对抗癌药物更敏感。
Eur J Surg Oncol. 1991 Feb;17(1):47-50.
4
Sensitivity to six antitumor drugs differs between primary and metastatic liver cancers.
Eur J Cancer Clin Oncol. 1988 Sep;24(9):1511-3. doi: 10.1016/0277-5379(88)90343-4.
5
Antitumor chemosensitivity differs between clinical sarcoma and adenocarcinoma tissues.
Anticancer Res. 1994 Jan-Feb;14(1A):169-71.
6
Colorectal carcinoma in vitro is more sensitive to 1-hexylcarbamoyl-5-fluorouracil compared with six other antitumor drugs: carboquone, Adriamycin, mitomycin C, aclacinomycin A, cisplatin, 5-fluorouracil.
Dis Colon Rectum. 1988 Jan;31(1):62-7. doi: 10.1007/BF02552573.
7
Chemosensitivity differences between primary and metastatic lesions of clinical gastric cancer.临床胃癌原发灶与转移灶之间的化疗敏感性差异。
Eur J Surg Oncol. 1988 Dec;14(6):685-9.
8
[The sensitivity of 1,000 human tumors to antitumor drugs using the succinate dehydrogenase inhibition (SDI) test].
Rinsho Byori. 1990 Nov;38(11):1273-8.
9
5-Fluorouracil is converted to F-nucleotides more extensively and is more cytotoxic in poorly differentiated than in well differentiated human gastric carcinoma.
Anticancer Res. 1990 Jul-Aug;10(4):1091-4.
10
[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.

引用本文的文献

1
Effects of aiton and the absorbed bioactive metabolite matrine individually and in combination with 5-fluorouracil on proliferation and apoptosis of gastric cancer cells in nude mice.氧化苦参碱及其吸收的生物活性代谢产物苦参碱单独及与5-氟尿嘧啶联合应用对裸鼠胃癌细胞增殖和凋亡的影响。
Front Pharmacol. 2022 Nov 9;13:1047507. doi: 10.3389/fphar.2022.1047507. eCollection 2022.
2
Deep Learning for Automatic Subclassification of Gastric Carcinoma Using Whole-Slide Histopathology Images.使用全切片组织病理学图像的深度学习对胃癌进行自动亚分类
Cancers (Basel). 2021 Jul 29;13(15):3811. doi: 10.3390/cancers13153811.
3
Initiation of inflammatory tumorigenesis by CTLA4 insufficiency due to type 2 cytokines.
由于 2 型细胞因子导致 CTLA4 不足引发炎症性肿瘤发生。
J Exp Med. 2018 Mar 5;215(3):841-858. doi: 10.1084/jem.20171971. Epub 2018 Jan 26.
4
Discrepancies in the histologic type between biopsy and resected specimens: a cautionary note for mixed-type gastric carcinoma.活检标本与切除标本组织学类型的差异:对混合型胃癌的警示
World J Gastroenterol. 2015 Apr 21;21(15):4673-9. doi: 10.3748/wjg.v21.i15.4673.
5
Histological mixed-type as an independent prognostic factor in stage I gastric carcinoma.组织学混合型作为Ⅰ期胃癌的独立预后因素。
World J Gastroenterol. 2015 Jan 14;21(2):549-55. doi: 10.3748/wjg.v21.i2.549.
6
Enhanced expression of DNA topoisomerase II genes in human medulloblastoma and its possible association with etoposide sensitivity.DNA拓扑异构酶II基因在人髓母细胞瘤中的表达增强及其与依托泊苷敏感性的可能关联。
J Neurooncol. 2007 Sep;84(2):119-29. doi: 10.1007/s11060-007-9360-0. Epub 2007 Mar 15.
7
A phase II study of combined chemotherapy with methotrexate, 5-fluorouracil, and low-dose cisplatin (MFP) for histologically diffuse-type advanced and recurrent gastric cancer (KDOG9501).一项关于甲氨蝶呤、5-氟尿嘧啶和低剂量顺铂联合化疗(MFP)用于组织学弥漫型晚期和复发性胃癌的II期研究(KDOG9501)。
Gastric Cancer. 2006;9(3):185-91. doi: 10.1007/s10120-006-0371-x.
8
Relationship of ECL cells and gastric neoplasia.肠嗜铬样细胞与胃肿瘤的关系。
Yale J Biol Med. 1998 May-Aug;71(3-4):325-35.
9
Histopathological assessment of multidrug resistance in gastric cancer: expression of P-glycoprotein, multidrug resistance-associated protein, and lung-resistance protein.胃癌多药耐药的组织病理学评估:P-糖蛋白、多药耐药相关蛋白和肺耐药蛋白的表达
Surg Today. 1999;29(5):401-6. doi: 10.1007/BF02483030.
10
Laser flow cytometric studies on the intracellular accumulation of anthracyclines when combined with heat.关于蒽环类药物与热联合使用时细胞内蓄积情况的激光流式细胞术研究。
Cancer Chemother Pharmacol. 1994;33(5):371-7. doi: 10.1007/BF00686265.