Establishment and Validation of Quantitative Real-time PCR Assay for Aberrant Methylation of 14-3-3Ï Gene in Breast and Lung Carcinoma
Background: 14-3-3Ï gene has been shown to be responsible for G2 cell cycle checkpoint control by p53 in response to DNA damage in human cells. In order to increase the potential utility of 14-3-3Ï gene as a molecular marker in tumor analysis and prognosis, we established and validated a quantitat...
Saved in:
| Published in: | Cancer genomics & proteomics Vol. 1; no. 1; p. 1 |
|---|---|
| Main Author: | |
| Format: | Journal Article |
| Language: | English |
| Published: |
International Institute of Anticancer Research
01-01-2004
|
| Online Access: | Get full text |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Summary: | Background: 14-3-3Ï gene has been shown to be responsible for G2 cell cycle checkpoint control by p53 in response to DNA damage
in human cells. In order to increase the potential utility of 14-3-3Ï gene as a molecular marker in tumor analysis and prognosis,
we established and validated a quantitative real-time MSP assay and correlated our findings with the standard MSP assay. Materials
and Methods: We examined the expression of 14-3-3 Ï gene by reverse transcription PCR (RT-PCR) in breast and lung cancer cell
lines and control non-malignant tissue samples. To elucidate the mechanism of gene silencing, we studied the methylation patterns
in cell lines, tumors and non-malignant control tissues of breast and lung using previously reported MSP assay. For fluorescence
based quantitative Real-Time PCR assay, we designed primers and probe specific to 14-3-3Ï gene, validated the assay in cell
lines and non-malignant control tissues of breast and lung and extended the study to primary tumors and corresponding non-malignant
tissues. Results: The concordances between the standard MSP assay and the real-time assay were 95-100%. The overall concordances
between standard MSP and real-time assay in 60 cell lines were 97%. By real-time assay, the differences in methylation frequencies
between malignant and non-malignant breast and between malignant and non-malignant lung tissues; between NSCLC and SCLC cell
lines; between MSP (-) and MSP (+) samples and between MSP (+) and MSP (++) samples were statistically significant. The mean
real-time values for MSP (-), MSP (+) and MSP (++) samples were 2, 28 and 53 respectively. Conclusion: We conclude that promoter
methylation is a valid pathway for silencing of 14-3-3Ï gene in primary breast and lung carcinomas. The real-time assay to
distinguish the extent and degree of methylation of 14-3-3Ï gene among malignant and non-malignant tissues would potentially
enhance the utility of this marker in breast and lung cancer analysis and prognosis. |
|---|---|
| ISSN: | 1109-6535 |