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正常细胞和肿瘤细胞中的APC基因产物。

The APC gene product in normal and tumor cells.

作者信息

Smith K J, Johnson K A, Bryan T M, Hill D E, Markowitz S, Willson J K, Paraskeva C, Petersen G M, Hamilton S R, Vogelstein B

机构信息

Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21231.

出版信息

Proc Natl Acad Sci U S A. 1993 Apr 1;90(7):2846-50. doi: 10.1073/pnas.90.7.2846.

Abstract

The APC gene has been found to be mutated during the development of sporadic colorectal tumors as well as in the germ line of familial adenomatous polyposis patients. To facilitate the characterization of both normal and mutant APC protein, a series of monoclonal and polyclonal antibodies specific for the APC protein was produced. When lymphoblastoid cell lines derived from seven familial adenomatous polyposis patients with known mutations were analyzed by Western blot, an approximately 300-kDa protein corresponding to the predicted size of full-length APC was detected in all 7 cell lines. In addition, truncated APC proteins corresponding to the product of the known mutated alleles could be detected in 4 of the 7 lines. Similar analysis of 23 colon carcinoma and 9 adenoma cell lines revealed truncated proteins in 24 (75%) of the cell lines. Moreover, 26 (81%) of the colon tumor lines were totally devoid of the normal, full-length protein. In contrast, Western blot analysis of 40 cell lines derived from sporadic tumors of other organs detected only full-length APC. Immunohistochemical analysis of APC in normal colonic mucosa revealed cytoplasmic staining with more intense staining in the basolateral margins of the epithelial cell. This staining was markedly increased in the upper portions of the crypts, suggesting an increased level of expression with maturation. These studies provide some initial clues to the function of the cytoplasmic protein APC and demonstrate the feasibility of identifying APC mutations by direct analysis of the APC protein.

摘要

已发现APC基因在散发性结直肠肿瘤发生过程中以及家族性腺瘤性息肉病患者的种系中发生突变。为便于对正常和突变型APC蛋白进行表征,制备了一系列针对APC蛋白的单克隆和多克隆抗体。当通过蛋白质印迹法分析来自7名已知突变的家族性腺瘤性息肉病患者的淋巴母细胞系时,在所有7个细胞系中均检测到一种约300 kDa的蛋白,其大小与全长APC的预测大小相符。此外,在7个细胞系中的4个中可检测到与已知突变等位基因产物相对应的截短型APC蛋白。对23个结肠癌细胞系和9个腺癌细胞系进行的类似分析显示,24个(75%)细胞系中存在截短型蛋白。此外,26个(81%)结肠肿瘤细胞系完全缺乏正常的全长蛋白。相比之下,对来自其他器官散发性肿瘤的40个细胞系进行蛋白质印迹分析仅检测到全长APC。对正常结肠黏膜中APC的免疫组织化学分析显示细胞质染色,上皮细胞基底外侧边缘染色更强。隐窝上部的这种染色明显增加,表明随着成熟表达水平升高。这些研究为细胞质蛋白APC的功能提供了一些初步线索,并证明了通过直接分析APC蛋白来鉴定APC突变的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/537f/46193/05365b42112e/pnas01466-0301-a.jpg

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