Development and evaluation of a colorimetric membrane-array method for the detection of circulating tumor cells in the peripheral blood of Taiwanese patients with colorectal cancer
Early detection is the hallmark of successful cancer treatment. Evidence is accumulating that primary cancers begin shedding neoplastic cells in the circulation at an early stage. To date, a high-sensitivity and high-throughput method for the detection of circulating tumor cells (CTCs) is deficient....
Gespeichert in:
Veröffentlicht in: | International journal of molecular medicine 2006-05, Vol.17 (5), p.737-747 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Early detection is the hallmark of successful cancer treatment. Evidence
is accumulating that primary cancers begin shedding neoplastic cells in the circulation
at an early stage. To date, a high-sensitivity and high-throughput method for
the detection of circulating tumor cells (CTCs) is deficient. In this study, we
have developed a high-sensitivity colorimetric membrane-array method to detect
CTCs in the peripheral blood of colorectal cancer (CRC) patients as a potential
diagnostic tool. Previously, we identified a set of 18 oligonucleotide clones,
significantly overexpressed in CRC, which were synthesized and applied to a nylon
membrane. Digoxigenin (DIG)-labeled cDNA were amplified by reverse transcriptase-polymerase
chain reaction (RT-PCR) from the peripheral blood of 88 Taiwanese CRC patients
and 50 healthy subjects, and were then hybridized to the membrane-array. Hybridization
signals were detected by color development. Meanwhile, blood samples were analyzed
by real-time quantitative PCR (Q-PCR). Subsequently, both methods were compared
regarding their correlation, sensitivity and specificity in the detection of CTCs
by statistics. The results of membrane-arrays were demonstrated to be closely
related to that of Q-PCR (P |
---|---|
ISSN: | 1107-3756 1791-244X |
DOI: | 10.3892/ijmm.17.5.737 |