Different transcriptional expression of KIAA1324 and its splicing variants in human carcinoma cell lines with different metastatic capacity

  • Authors:
    • Mario Bauer
    • Gabi Aust
    • Udo Schumacher
  • View Affiliations

  • Published online on: March 1, 2004     https://doi.org/10.3892/or.11.3.677
  • Pages: 677-680
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Abstract

To identify new genes involved in metastasis, we compared the cDNA patterns of the high-metastatic MCF-7 and non-metastatic Hbl100 breast tumor cell lines by subtractive hybridization and verified the results by real-time RT-PCR in various carcinoma cell lines. One of the differentially expressed genes is KIAA1324, which is overexpressed in some high-metastatic breast and lung cancer cell lines. We have found two new splice variants of KIAA1324 mRNA in non-metastatic carcinoma cell lines and normal epithelial cells that predict the existence of truncated proteins. In summary, KIAA1324 could be involved in tumor progression and metastasis either by its expression level or through variable expression of alternative splice products.

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March 2004
Volume 11 Issue 3

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

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Spandidos Publications style
Bauer M, Aust G and Schumacher U: Different transcriptional expression of KIAA1324 and its splicing variants in human carcinoma cell lines with different metastatic capacity. Oncol Rep 11: 677-680, 2004
APA
Bauer, M., Aust, G., & Schumacher, U. (2004). Different transcriptional expression of KIAA1324 and its splicing variants in human carcinoma cell lines with different metastatic capacity. Oncology Reports, 11, 677-680. https://doi.org/10.3892/or.11.3.677
MLA
Bauer, M., Aust, G., Schumacher, U."Different transcriptional expression of KIAA1324 and its splicing variants in human carcinoma cell lines with different metastatic capacity". Oncology Reports 11.3 (2004): 677-680.
Chicago
Bauer, M., Aust, G., Schumacher, U."Different transcriptional expression of KIAA1324 and its splicing variants in human carcinoma cell lines with different metastatic capacity". Oncology Reports 11, no. 3 (2004): 677-680. https://doi.org/10.3892/or.11.3.677