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人乳腺癌相关抗原对白细胞迁移的抑制作用。

Inhibition of leukocyte migration by human breast-cancer-associated antigens.

作者信息

Kadish A S, Marcus D M, Bloom B R

出版信息

Int J Cancer. 1976 Nov 15;18(5):581-6. doi: 10.1002/ijc.2910180506.

Abstract

The existence of CMI to tumor-associated antigens present in 3 M KCl extracts of breast carcinomas was demonstrated in a group of breast cancer patients by the leukocyte migration inhibition (LMI) assay. When crude KCl extracts were tested, 3 of 5 breast cancer patients gave a positive response to autologous tumor extracts. Eleven of 20 gave a positive response to allogeneic extracts as compared to 3 of 22 controls (including 6 patients with benign breast disease, 7 with non-mammary cancers and 9 normal controls). Extracts of fibrocystic disease tissue gave positive LMI tests in 2 of 5 breast cancer patients, suggesting the presence of antigenic cross-reactivity between benign and malignant breast disease. An extract of a medullary carcinoma of breast was fractionated on Sephadex G-200 and the effluent pooled into three fractions. The high molecular weight fraction produced LMI in 11 of 22 breast cancer patients and in 1 of 19 controls, including patients with benign breast disease, other cancers and normal individuals. The low molecular weight fraction produced LMI in both the benign (4 of 6) and the malignant breast disease (6 of 20) patients, but not in the controls (0 of 12). A simple fractionation technique has thus separated "cancer-specific" from "organ-specific" activity. Sephadex G-200 fractions were active at a much lower protein concentration than the crude 3 M KCl extracts.

摘要

通过白细胞迁移抑制(LMI)试验,在一组乳腺癌患者中证实了对乳腺癌3M KCl提取物中存在的肿瘤相关抗原的细胞介导免疫(CMI)的存在。当检测粗制KCl提取物时,5名乳腺癌患者中有3名对自体肿瘤提取物呈阳性反应。20名患者中有11名对同种异体提取物呈阳性反应,而22名对照者(包括6名乳腺良性疾病患者、7名非乳腺癌患者和9名正常对照者)中有3名呈阳性反应。纤维囊性疾病组织提取物在5名乳腺癌患者中有2名LMI试验呈阳性,提示乳腺良性和恶性疾病之间存在抗原交叉反应。对乳腺髓样癌提取物在Sephadex G - 200上进行分级分离,流出物合并为三个级分。高分子量级分在22名乳腺癌患者中有11名产生LMI,在19名对照者(包括乳腺良性疾病患者、其他癌症患者和正常个体)中有1名产生LMI。低分子量级分在乳腺良性疾病患者(6名中有4名)和乳腺恶性疾病患者(20名中有6名)中均产生LMI,但在对照者(12名中有0名)中未产生。因此,一种简单的分级分离技术已将“癌症特异性”活性与“器官特异性”活性分开。Sephadex G - 200级分在比粗制3M KCl提取物低得多的蛋白质浓度下具有活性。

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