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Detection of activated KRAS from cancer patient peripheral blood using a weighted enzymatic chip array
BACKGROUND: The KRAS oncogene was one of the earliest discoveries of genetic alterations in colorectal and lung cancers. Moreover, KRAS somatic mutations might be used for predicting the efficiency of anti-EGFR therapeutic drugs. The purpose of this research was to improve Activating KRAS Detection...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055935/ https://www.ncbi.nlm.nih.gov/pubmed/24884535 http://dx.doi.org/10.1186/1479-5876-12-147 |
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author | Huang, Ming-Yii Liu, Hsueh-Chiao Yen, Li-Chen Chang, Jia-Yuan Huang, Jian-Jhang Wang, Jaw-Yuan Hsiao, Chao-Peng Lin, Shiu-Ru |
author_facet | Huang, Ming-Yii Liu, Hsueh-Chiao Yen, Li-Chen Chang, Jia-Yuan Huang, Jian-Jhang Wang, Jaw-Yuan Hsiao, Chao-Peng Lin, Shiu-Ru |
author_sort | Huang, Ming-Yii |
collection | PubMed |
description | BACKGROUND: The KRAS oncogene was one of the earliest discoveries of genetic alterations in colorectal and lung cancers. Moreover, KRAS somatic mutations might be used for predicting the efficiency of anti-EGFR therapeutic drugs. The purpose of this research was to improve Activating KRAS Detection Chip by using a weighted enzymatic chip array (WEnCA) platform to detect activated KRAS mutations status in the peripheral blood of non-small-cell lung cancer (NSCLC) and colorectal cancer (CRC) patients in Taiwan. METHODS: Our laboratory developed an Activating KRAS Detection Chip and a WEnCA technique that can detect activated KRAS mutation status by screening circulating cancer cells in the surrounding bloodstream. We collected 390 peripheral blood samples of NSCLC patients (n = 210) and CRC patients (n = 180) to evaluate clinical KRAS activation using this gene array diagnosis apparatus, an Activating KRAS Detection Chip and a WEnCA technique. Subsequently, we prospectively enrolled 88 stage III CRC patients who received adjuvant FOLFOX-4 chemotherapy with or without cetuximab. We compared the chip results of preoperative blood specimens and their relationship with disease control status in these patients. RESULTS: After statistical analysis, the sensitivity of WEnCA was found to be 93%, and the specificity was found to be 94%. Relapse status and chip results among the stage III CRC patients receiving FOLFOX-4 plus cetuximab (n = 59) and those receiving FOLFOX-4 alone (n = 29) were compared. Among the 51 stage III CRC patients with chip negative results who were treated with FOLFOX-4 plus cetuximab chemotherapy, the relapse rate was 33.3%; otherwise, the relapse rate was 48.5% among the 23 out of 88 patients with chip negative results who received FOLFOX-4 alone. Negative chip results were significantly associated to better treatment outcomes in the FOLFOX-4 plus cetuximab group (P = 0.047). CONCLUSIONS: The results demonstrated that the WEnCA technique is a sensitive and convenient technique that produces easy-to-interpret results for detecting activated KRAS from the peripheral blood of cancer patients. We suggest that the WEnCA technique is also a potential tool for predicting responses in CRC patients following FOLFOX-4 plus cetuximab chemotherapy. |
format | Online Article Text |
id | pubmed-4055935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40559352014-06-14 Detection of activated KRAS from cancer patient peripheral blood using a weighted enzymatic chip array Huang, Ming-Yii Liu, Hsueh-Chiao Yen, Li-Chen Chang, Jia-Yuan Huang, Jian-Jhang Wang, Jaw-Yuan Hsiao, Chao-Peng Lin, Shiu-Ru J Transl Med Research BACKGROUND: The KRAS oncogene was one of the earliest discoveries of genetic alterations in colorectal and lung cancers. Moreover, KRAS somatic mutations might be used for predicting the efficiency of anti-EGFR therapeutic drugs. The purpose of this research was to improve Activating KRAS Detection Chip by using a weighted enzymatic chip array (WEnCA) platform to detect activated KRAS mutations status in the peripheral blood of non-small-cell lung cancer (NSCLC) and colorectal cancer (CRC) patients in Taiwan. METHODS: Our laboratory developed an Activating KRAS Detection Chip and a WEnCA technique that can detect activated KRAS mutation status by screening circulating cancer cells in the surrounding bloodstream. We collected 390 peripheral blood samples of NSCLC patients (n = 210) and CRC patients (n = 180) to evaluate clinical KRAS activation using this gene array diagnosis apparatus, an Activating KRAS Detection Chip and a WEnCA technique. Subsequently, we prospectively enrolled 88 stage III CRC patients who received adjuvant FOLFOX-4 chemotherapy with or without cetuximab. We compared the chip results of preoperative blood specimens and their relationship with disease control status in these patients. RESULTS: After statistical analysis, the sensitivity of WEnCA was found to be 93%, and the specificity was found to be 94%. Relapse status and chip results among the stage III CRC patients receiving FOLFOX-4 plus cetuximab (n = 59) and those receiving FOLFOX-4 alone (n = 29) were compared. Among the 51 stage III CRC patients with chip negative results who were treated with FOLFOX-4 plus cetuximab chemotherapy, the relapse rate was 33.3%; otherwise, the relapse rate was 48.5% among the 23 out of 88 patients with chip negative results who received FOLFOX-4 alone. Negative chip results were significantly associated to better treatment outcomes in the FOLFOX-4 plus cetuximab group (P = 0.047). CONCLUSIONS: The results demonstrated that the WEnCA technique is a sensitive and convenient technique that produces easy-to-interpret results for detecting activated KRAS from the peripheral blood of cancer patients. We suggest that the WEnCA technique is also a potential tool for predicting responses in CRC patients following FOLFOX-4 plus cetuximab chemotherapy. BioMed Central 2014-05-26 /pmc/articles/PMC4055935/ /pubmed/24884535 http://dx.doi.org/10.1186/1479-5876-12-147 Text en Copyright © 2014 Huang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Huang, Ming-Yii Liu, Hsueh-Chiao Yen, Li-Chen Chang, Jia-Yuan Huang, Jian-Jhang Wang, Jaw-Yuan Hsiao, Chao-Peng Lin, Shiu-Ru Detection of activated KRAS from cancer patient peripheral blood using a weighted enzymatic chip array |
title | Detection of activated KRAS from cancer patient peripheral blood using a weighted enzymatic chip array |
title_full | Detection of activated KRAS from cancer patient peripheral blood using a weighted enzymatic chip array |
title_fullStr | Detection of activated KRAS from cancer patient peripheral blood using a weighted enzymatic chip array |
title_full_unstemmed | Detection of activated KRAS from cancer patient peripheral blood using a weighted enzymatic chip array |
title_short | Detection of activated KRAS from cancer patient peripheral blood using a weighted enzymatic chip array |
title_sort | detection of activated kras from cancer patient peripheral blood using a weighted enzymatic chip array |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055935/ https://www.ncbi.nlm.nih.gov/pubmed/24884535 http://dx.doi.org/10.1186/1479-5876-12-147 |
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