ELISA-based Ki-ras gene mutation analyses in pancreatic and cholangiocarcinoma cells and tissues

  • Authors:
    • Marcin Gabriel
    • Doris Henne-Bruns
    • Holger Kalthoff
  • View Affiliations

  • Published online on: November 1, 2001     https://doi.org/10.3892/or.8.6.1367
  • Pages: 1367-1370
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Abstract

Detection of Ki-ras mutations is one possible modality for diagnosis of human neoplasms, particularly of the gastrointestinal tract. Little is known about the protein expression levels of ras p21. Here we show a semi-quantitative analysis of mutated ras p21 in protein extracts from pancreatic and cholangiocarcinoma cell lines and from tumor tissues. Comparison with DNA sequencing data confirmed the specificity of the ELISA-mediated mutation analysis. Epithelial cell content from stroma rich tissues was estimated by measuring the CK 8, 18 and 19 concentration in protein extracts from tissue samples comparing this with the average keratin content in extracts from 21 GI-carcinoma cell lines. The combination of both tests allowed the analysis of the ras p21 content of tissues with as little as 5% tumor cell content.

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November-December 2001
Volume 8 Issue 6

Print ISSN: 1021-335X
Online ISSN:1791-2431

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Spandidos Publications style
Gabriel M, Henne-Bruns D and Kalthoff H: ELISA-based Ki-ras gene mutation analyses in pancreatic and cholangiocarcinoma cells and tissues. Oncol Rep 8: 1367-1370, 2001
APA
Gabriel, M., Henne-Bruns, D., & Kalthoff, H. (2001). ELISA-based Ki-ras gene mutation analyses in pancreatic and cholangiocarcinoma cells and tissues. Oncology Reports, 8, 1367-1370. https://doi.org/10.3892/or.8.6.1367
MLA
Gabriel, M., Henne-Bruns, D., Kalthoff, H."ELISA-based Ki-ras gene mutation analyses in pancreatic and cholangiocarcinoma cells and tissues". Oncology Reports 8.6 (2001): 1367-1370.
Chicago
Gabriel, M., Henne-Bruns, D., Kalthoff, H."ELISA-based Ki-ras gene mutation analyses in pancreatic and cholangiocarcinoma cells and tissues". Oncology Reports 8, no. 6 (2001): 1367-1370. https://doi.org/10.3892/or.8.6.1367