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• W2900561903 endingPage "446" @default.
• W2900561903 startingPage "446" @default.
• W2900561903 abstract "Predicting a patient’s risk of recurrence after the resection of liver metastases from colorectal cancer is critical for evaluating and selecting therapeutic approaches. Clinical and pathologic parameters have shown limited accuracy thus far. Therefore, we combined the clinical status with a genomic approach to stratify relapse-free survival in colorectal cancer liver metastases patients. To identify new molecular and genetic signatures specific to colorectal cancer with liver metastasis (CRCLM) patients, we conducted DNA copy number profiling on a cohort of 21 Taiwanese CRCLM patients using a comparative genomic hybridization (CGH) array. We identified a three-gene signature based on differential copy number alteration between patients with different statuses of (1) recurrence and (2) synchronous metastasis. In relapse hotspot regions, only three genes (S100PBP, CSMD2, and TGFBI) were significantly associated with the synchronous liver metastasis factor. A final set of three genes—S100PBP, CSMD2, TGFBI—significantly predicted relapse-free survival in our cohort (p = 0.04) and another CRCLM cohort (p = 0.02). This three-gene signature is the first genomic signature validated for relapse-free survival in post-hepatectomy CRCLM patients. Our three-gene signature was developed using a whole-genome CGH array and has a good prognostic position for the relapse-free survival of CRCLM patients after hepatectomy." @default.
• W2900561903 created "2018-11-29" @default.
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• W2900561903 date "2018-11-18" @default.
• W2900561903 modified "2023-10-14" @default.
• W2900561903 title "Genome-Wide Scan for Copy Number Alteration Association with Relapse-Free Survival in Colorectal Cancer with Liver Metastasis Patients" @default.
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• W2900561903 doi "https://doi.org/10.3390/jcm7110446" @default.
• W2900561903 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6262537" @default.
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• W2900561903 hasPublicationYear "2018" @default.
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