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卵巢癌细胞对抗癌化疗药物敏感性测试的研究——特别参考乳酸脱氢酶及其同工酶作为指标的应用(作者译)

[A study on sensitivity testing of ovarian cancer cells to anticancer chemotherapy - with special reference to the use of LDH and its isozymes as indicators (author's transl)].

作者信息

Inui H, Yasuda M, Yoshioka M, Morimoto O, Terashima Y, Hachiya S

出版信息

Nihon Sanka Fujinka Gakkai Zasshi. 1981 Dec;33(12):2182-6.

PMID:7338669
Abstract

The malignant ovarian cancer cells removed on operation were cultured and exposed to the anticancer drug (either 5-fluorouracil or mitomycin C) for 30 minutes or 24 hours respectively. The activity of the LDH and LDH isozyme in the culture medium was measured. Also the activity of the LDH and its isozyme was determined in the patients undergoing chemotherapy with either 5-fluorouracil or mitomycin C. The results are summarized as follows: 1) The LDH isozyme pattern of the culture medium prior to exposure of malignant cells to the anticancer drugs was classified into 2 types i.e., M type which is characterized by a predominance of LDH4,5 (referred hereinafter to as group M) and H type with a predominance of LDH1,2 (referred to as group H). 2) Of 11 cases studied, 7 were classified as group M and 4 were categorized as group H. there was no distinct relationship between histological type and LDH isozyme pattern. 3) In the group with exposure to anticancer drugs the total LDH activity in both group H and group M was lower than in the control group. Control specimens in group H showed increased total LDH activity. 4) The H/M ratio based on subunits of LDH isozyme was virtually unchanged by exposure to anticancer drugs in group M, while rapidly lowered by the same treatment in group H. 5) The death rate of malignant cells as estimated by dye exclusion methods was higher with exposure to anticancer drugs than without it. 6) The serum LDH was more markedly lowered after treatment in group H than in group M. However, there was no substantial difference between the two groups in M/H ratio before and after treatment.

摘要

将手术切除的恶性卵巢癌细胞进行培养,并分别用抗癌药物(5-氟尿嘧啶或丝裂霉素C)处理30分钟或24小时。测定培养基中乳酸脱氢酶(LDH)及其同工酶的活性。同时也测定了接受5-氟尿嘧啶或丝裂霉素C化疗的患者体内LDH及其同工酶的活性。结果总结如下:1)恶性细胞接触抗癌药物之前,培养基中LDH同工酶模式分为2种类型,即M型,其特征是LDH4、5占优势(以下简称M组)和H型,其特征是LDH1、2占优势(简称H组)。2)在研究的11例病例中,7例归为M组,4例归为H组。组织学类型与LDH同工酶模式之间无明显关系。3)在接触抗癌药物的组中,H组和M组的总LDH活性均低于对照组。H组的对照标本显示总LDH活性增加。4)基于LDH同工酶亚基的H/M比值,M组接触抗癌药物后基本不变,而H组经相同处理后迅速降低。5)通过染料排斥法估计,接触抗癌药物的恶性细胞死亡率高于未接触的。6)治疗后,H组血清LDH降低比M组更明显。然而,两组治疗前后的M/H比值无实质性差异。

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[Biochemical activity in peritoneal effusion of ovarian malignancy].
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