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[通过SDI(琥珀酸脱氢酶抑制)试验评估的各种人类肿瘤的体外化学敏感性]

[In vitro chemosensitivity of various human tumors evaluated by the SDI (succinate dehydrogenase inhibition) test].

作者信息

Maehara Y, Anai H, Masuda H, Tamada R, Sugimachi K, Inokuchi K

出版信息

Gan To Kagaku Ryoho. 1985 Oct;12(10):2018-23.

PMID:4051518
Abstract

In vitro chemosensitivity was evaluated by SDI test in various human tumors including 1 lymph node metastasis of esophageal cancer, 10 gastric cancers, 4 colo-rectal cancers, 1 hepatoma, 2 lung cancers, 2 breast cancers and 1 gallbladder cancer. Tumor fragments cut with scissors were exposed to twelve kinds of antitumor drugs at five to ten times peak plasma concentration. After 3 days at 37 degrees C, each tumor fragment suspension was washed with phosphate-buffered saline and assayed for succinate dehydrogenase (SD) activity using 3-(4,5- dimethyl-2-thiazolyl)-2, 5-diphenyl-2H tetrazolium bromide (MTT) as a hydrogen acceptor. When the SD activity of the drug-treated cells was reduced to below 50% that of control cells, the chemosensitivity to the antitumor drug was considered positive. The chemosensitivity of each tumor varied individually. Mitomycin C or 5-fluorouracil are regularly used to treat gastric cancer patients, but, some specimens of gastric cancer in this study showed a resistance to these drugs and an unexpected sensitivity to other drugs. Our results show that the SDI test is a convenient method for clinical use and gives significant information about drug sensitivity.

摘要

通过SDI试验评估了包括1例食管癌淋巴结转移、10例胃癌、4例结直肠癌、1例肝癌、2例肺癌、2例乳腺癌和1例胆囊癌在内的各种人类肿瘤的体外化学敏感性。用剪刀剪下的肿瘤组织块暴露于12种抗肿瘤药物中,药物浓度为血浆峰值浓度的5至10倍。在37℃下培养3天后,用磷酸盐缓冲盐水洗涤每个肿瘤组织块悬液,并使用3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2H溴化四氮唑(MTT)作为氢受体测定琥珀酸脱氢酶(SD)活性。当药物处理细胞的SD活性降低至对照细胞的50%以下时,认为对该抗肿瘤药物的化学敏感性为阳性。每个肿瘤的化学敏感性各不相同。丝裂霉素C或5-氟尿嘧啶常用于治疗胃癌患者,但本研究中的一些胃癌标本对这些药物耐药,而对其他药物表现出意外的敏感性。我们的结果表明,SDI试验是一种便于临床使用的方法,能提供有关药物敏感性的重要信息。

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