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人结肠直肠癌中乳糖结合凝集素的表达。与肿瘤进展的关系。

Lactose-binding lectin expression in human colorectal carcinomas. Relation to tumor progression.

作者信息

Lotan R, Matsushita Y, Ohannesian D, Carralero D, Ota D M, Cleary K R, Nicolson G L, Irimura T

机构信息

Department of Tumor Biology, University of Texas M.D. Anderson Cancer Center, Houston 77030.

出版信息

Carbohydr Res. 1991 Jun 25;213:47-57. doi: 10.1016/s0008-6215(00)90597-4.

Abstract

Lactose-binding lectins having Mr values of approximately 14,000 (L-14.5) and approximately 35,000 Da have been found in a variety of vertebrate tissues, including normal intestine and colon, and in several types of tumors such as colon carcinomas. To determine the clinical relevance of such lectins in human colon cancer, specimens from 46 patients with colorectal carcinoma of identified Dukes' stages were selected and analyzed for the presence and amount of lactose-binding lectins by immunoblotting using a polyclonal, rabbit anti-lectin antibody followed by binding of 125I-labeled anti-rabbit IgG. The amount of a lectin having an Mr value of approximately 31,000 Da (L-31) varied among the specimens. The levels of L-31 lectin in colorectal cancer specimens from primary tumors of patients with distant metastases (Dukes' stage D) were significantly higher than were those from patients without detectable metastases (Dukes' stages B1 and B2). In contrast, among the various specimens the variation in the level of the L-14.5 lectin was smaller, and there was no correlation between the amount of this lectin and cancer stage. Immunohistochemical staining of thin sections of colorectal tumor specimens using antibodies specific for either L-31 or L-14.5 lectin revealed that the two were located at different places, the L-31 lectin primarily within the cytoplasm of carcinoma cells, and the L-14.5 lectin associated with secreted material. These results indicated that the relative amount of the L-31 lectin increases as the colorectal cancer progresses to a more malignant stage.

摘要

在包括正常肠道和结肠在内的多种脊椎动物组织以及几种肿瘤类型(如结肠癌)中,已发现分子量约为14,000(L - 14.5)和约35,000道尔顿的乳糖结合凝集素。为了确定此类凝集素在人类结肠癌中的临床相关性,选取了46例已确定Dukes分期的结直肠癌患者的标本,先用多克隆兔抗凝集素抗体进行免疫印迹分析乳糖结合凝集素的存在和含量,然后用125I标记的抗兔IgG进行结合。分子量约为31,000道尔顿(L - 31)的凝集素含量在各标本中有所不同。远处转移患者(Dukes分期D)原发肿瘤的结直肠癌标本中L - 31凝集素水平显著高于无转移患者(Dukes分期B1和B2)。相比之下,在各种标本中,L - 14.5凝集素水平的变化较小,且该凝集素的含量与癌症分期之间无相关性。使用针对L - 31或L - 14.5凝集素的特异性抗体对结直肠癌标本薄片进行免疫组织化学染色显示,二者位于不同位置,L - 31凝集素主要位于癌细胞胞质内,L - 14.5凝集素与分泌物质相关。这些结果表明,随着结直肠癌进展到更恶性阶段,L - 31凝集素的相对含量增加。

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