Abstract
Purpose: We have developed a real-time semiquantitative gap ligase chain reaction for detecting p53 point mutations at low level in a background of excess of wild-type DNA. Experimental Design: This method was validated by direct comparison to a previously validated but cumbersome phage plaque hybridization assay. Forty-one surgical margins and lymph nodes from 10 cases of head and neck squamous cell carcinoma and lung carcinoma were tested for p53 mutant clones. Results: Both methods detected p53 mutants in margins from 8 of the 10 cases, whereas standard pathology detected cancer cells in only 3 cases. Positive margins included tissue samples with a tumor/normal DNA ratio of up to 1:1000. Conclusions: This novel molecular approach can be performed in <5 h facilitating intraoperative use for real-time surgical resection.
Original language | English (US) |
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Pages (from-to) | 2379-2385 |
Number of pages | 7 |
Journal | Clinical Cancer Research |
Volume | 10 |
Issue number | 7 |
DOIs | |
State | Published - Apr 1 2004 |
ASJC Scopus subject areas
- Oncology
- Cancer Research