کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2112882 | 1084428 | 2013 | 7 صفحه PDF | دانلود رایگان |

The characterization of circulating tumor cells (CTCs) could substantially improve the management of cancer patients. However, their study is still a matter of debate, often due to lymphocyte contamination. In the present paper, an investigation of CTCs was carried out for the first time using DEPArray, a dielectrophoresis-based platform able to detect and sort pure CTCs. Analyses were conducted on peripheral blood (PB) samples from patients with metastatic colon cancer. After 100% pure cell recovery and whole genome amplification, KRAS gene mutation of CTCs was screened and compared to gene status in the primary tumor tissue. CTCs were found in 21 colon cancer patients (52.5%), with more than three tumor cells per 7.5 ml. KRAS gene mutation analysis, showed a mutational concordance between CTCs and primary tumor in 50% of matched cases. The present study demonstrates for the first time the feasibility of analyzing at the molecular level pure CTCs avoiding lymphocyte contamination using an innovative instrumentation, and a KRAS discordance between CTCs and primary tissue. Our results present dielectrophoresis-based procedures as a new standard in single cell analysis and recovery and invite careful reflection on the value of CTCs characterization.
► The study was performed using a DEP-based device to detect and sort 100% pure CTCs.
► Analyses were conducted on blood from 40 patients with metastatic colon cancer.
► CTCs were found in 21 patients.
► A difference in KRAS status between CTCs and primary tumor was observed in 8 cases.
► Our DEP-based assay invites reflection on the value of CTC characterization.
Journal: Cancer Letters - Volume 335, Issue 1, 10 July 2013, Pages 225–231