p53 Mutations in Primary and Metastatic Tumors and Circulating Tumor Cells from Colorectal Carcinoma Patients
Circulating tumor cells could provide a relatively noninvasive and repeatable source of information about tumor cell genotype that might influence treatment and estimation of prognosis. We developed a technique for identifying p53 mutations in tumor cells isolated from the peripheral venous blood of...
Saved in:
Published in | Clinical cancer research Vol. 6; no. 9; pp. 3499 - 3504 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Association for Cancer Research
01.09.2000
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Circulating
tumor cells could provide a relatively noninvasive and repeatable
source of information about tumor cell genotype that might influence
treatment and estimation of prognosis. We developed a technique for
identifying p53 mutations in tumor cells isolated from
the peripheral venous blood of colorectal cancer patients and compared
the prevalence and position of these mutations with multiple solid
tumor samples from the same patient. We used immunomagnetic beads to
isolate tumor cells, reverse transcriptase-nested polymerase chain
amplification of the coding region between exons 4 and 9 within the
p53 gene, and automated gene sequencing. Nineteen
p53 mutations were detected in solid tumor samples from
19 of 41 colorectal carcinoma patients. An identical p53
mutation was invariably present in all samples from primary and
metastatic colorectal tumor biopsies within the same patient.
p53 mutations were detected in peripheral blood from 8
of these 19 patients with p53 -mutated solid tumors.
Where identified, the pattern of mutation in peripheral blood samples
was invariably the same as in matching solid tumor samples. A single
colorectal carcinoma biopsy provided reliable p53 gene
mutational information in colorectal carcinoma. Detection of this
p53 mutation in tumor cells from peripheral blood was
achieved with an approach based on cell selection for epithelial
characteristics, reverse transcription-PCR, and gene sequencing. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1078-0432 1557-3265 |