DC Field | Value | Language |
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dc.contributor.author | Seon-Kyu Kim | - |
dc.contributor.author | Seon-Young Kim | - |
dc.contributor.author | Jeong Hwan Kim | - |
dc.contributor.author | S A Rho | - |
dc.contributor.author | D H Cho | - |
dc.contributor.author | Yong Sung Kim | - |
dc.contributor.author | J C Kim | - |
dc.date.accessioned | 2017-04-19T09:57:58Z | - |
dc.date.available | 2017-04-19T09:57:58Z | - |
dc.date.issued | 2014 | - |
dc.identifier.issn | 1574-7891 | - |
dc.identifier.uri | 10.1016/j.molonc.2014.06.016 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/12262 | - |
dc.description.abstract | Colorectal cancer (CRC) patients frequently experience disease recurrence and distant metastasis. This study aimed to identify prognostic indicators, including individual responses to chemotherapy, in CRC patients. RNA-seq data was generated using 54 samples (normal colon, primary CRC, and liver metastases) from 18 CRC patients and genes associated with CRC aggressiveness were identified. A risk score based on these genes was developed and validated in four independent CRC patient cohorts ( n=1063). Diverse statistical methods were applied to validate the risk scoring system, including a generalized linear model likelihood ratio test, Kaplan-Meier curves, a log-rank test, and the Cox model. TREM1 and CTGF were identified as two activated regulators associated with CRC aggressiveness. A risk score based on 19 genes regulated by TREM1 or CTGF activation (TCA19) was a significant prognostic indicator. In multivariate and subset analyses based on pathological staging, TCA19 was an independent risk factor (HR=1.894, 95% CI=1.227-2.809, P=0.002). Subset stratification in stage III patients revealed that TCA19 had prognostic potential and identified patients who would benefit from adjuvant chemotherapy, regardless of age. The TCA19 predictor represents a novel diagnostic tool for identifying high-risk CRC patients and possibly predicting the response to adjuvant chemotherapy. ⓒ 2014 Federation of European Biochemical Societies. | - |
dc.publisher | Wiley | - |
dc.title | A nineteen gene-based risk score classifier predicts prognosis of colorectal cancer patients | - |
dc.title.alternative | A nineteen gene-based risk score classifier predicts prognosis of colorectal cancer patients | - |
dc.type | Article | - |
dc.citation.title | Molecular Oncology | - |
dc.citation.number | 8 | - |
dc.citation.endPage | 1666 | - |
dc.citation.startPage | 1653 | - |
dc.citation.volume | 8 | - |
dc.contributor.affiliatedAuthor | Seon-Kyu Kim | - |
dc.contributor.affiliatedAuthor | Seon-Young Kim | - |
dc.contributor.affiliatedAuthor | Jeong Hwan Kim | - |
dc.contributor.affiliatedAuthor | Yong Sung Kim | - |
dc.contributor.alternativeName | 김선규 | - |
dc.contributor.alternativeName | 김선영 | - |
dc.contributor.alternativeName | 김정환 | - |
dc.contributor.alternativeName | 노선애 | - |
dc.contributor.alternativeName | 조동형 | - |
dc.contributor.alternativeName | 김용성 | - |
dc.contributor.alternativeName | 김진천 | - |
dc.identifier.bibliographicCitation | Molecular Oncology, vol. 8, no. 8, pp. 1653-1666 | - |
dc.identifier.doi | 10.1016/j.molonc.2014.06.016 | - |
dc.subject.keyword | Chemotherapy | - |
dc.subject.keyword | Colorectal cancer | - |
dc.subject.keyword | Markers | - |
dc.subject.keyword | Metastasis | - |
dc.subject.keyword | Prognosis | - |
dc.subject.local | Chemotherapy | - |
dc.subject.local | chemotherapy | - |
dc.subject.local | Colorectal cancer | - |
dc.subject.local | colorectal cancer | - |
dc.subject.local | Colorectal Cancer | - |
dc.subject.local | marker | - |
dc.subject.local | markers | - |
dc.subject.local | Marker | - |
dc.subject.local | Markers | - |
dc.subject.local | makers | - |
dc.subject.local | metastasis | - |
dc.subject.local | Metastasis | - |
dc.subject.local | Prognosis | - |
dc.subject.local | prognosis | - |
dc.description.journalClass | Y | - |
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