Metastatic transcriptional pattern revealed by gene expression profiling in primary colorectal carcinoma

Antonello D'Arrigo, Claudio Belluco, Alessandro Ambrosi, Maura Digito, Giovanni Esposito, Antonella Bertola, Michele Fabris, Valentina Nofrate, Enzo Mammano, Alberta Leon, Donato Nitti, Mario Lise

Research output: Contribution to journalArticlepeer-review


Metastatic spread to the liver is the major contributor to mortality in patients with colorectal carcinoma (CRC). In order to seek for gene expression patterns associated with metastatic potential in primary CRC, we compared the transcriptional profiles of 10 radically resected primary CRCs from patients who did not develop distant metastases within a 5-year follow-up period with those of 10 primary/metastatic tumor pairs from patients with synchronous liver metastases. To focus selectively on neoplastic cells, the study was conducted on laser-microdissected bioptic tissues. Arrays of 7,864 human cDNAs were utilized. While a striking transcriptional similarity was observed between the primary tumors and their distant metastases, the nonmetastasizing primary tumors were clearly distinct from the primary/metastatic tumor pairs. Of 37 gene expression differences found between the 2 groups of primary tumors, 29 also distinguished nonmetastasizing tumors from metastases. The gene encoding for mannosyl (α-1,3-)-glycoprotein β-1,4-N-acetyl-glucosaminyl- transferase (GnT-IV) became significantly upregulated in primary/metastatic tumor pairs (p <0.001). GnT-IV upregulation was confirmed by RT-PCR. These data support the existence of a specific transcriptional signature distinguishing primary colon adenocarcinomas with different metastatic potential, the further pursuit of which may lead to relevant clinical and therapeutic applications.

Original languageEnglish
Pages (from-to)256-262
Number of pages7
JournalInternational Journal of Cancer
Issue number2
Publication statusPublished - Jun 10 2005


  • Colorectal cancer
  • DNA microarray
  • Metastasis

ASJC Scopus subject areas

  • Cancer Research
  • Oncology


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