| Literature DB >> 28521493 |
Naoto Yamamoto1, Takashi Oshima1, Kazue Yoshihara1, Toru Aoyama1, Tsutomu Hayashi1, Takanobu Yamada1, Tsutomu Sato1, Manabu Shiozawa1, Takaki Yoshikawa1, Soichiro Morinaga1, Yasushi Rino1, Chikara Kunisaki2, Katsuaki Tanaka2, Makoto Akaike1, Toshio Imada1, Munetaka Masuda1.
Abstract
The insulin-like growth factors (IGF) system is involved in tumor proliferation, invasion and metastasis in cancer. The current study investigated the association of IGF-1, IGF-2 and IGF-1 receptor (IGF-1R), IGF binding proteins type 3 (IGFBP-3) mRNA expression levels with clinicopathological characteristics and outcomes of 202 patients with untreated colorectal cancer (CRC). IGF-1, IGF-2, IGF-1R and IGFBP-3 mRNA expression levels were analyzed in surgical specimens of cancer tissues and adjacent normal mucosa cells using reverse transcription-quantitative polymerase chain reaction. The IGF-1R gene expression level was significantly higher in cancer tissue compared with adjacent normal mucosa. By contrast, IGF-1 gene expression levels were reduced in cancer tissue compared with normal mucosa. IGF-2 and IGFBP-3 gene expression levels did not differ significantly between cancer tissue and adjacent normal mucosa. As for the association of gene expression and clinicopathological characteristics, IGFBP-3 gene expression was significantly associated with lymph node metastasis. High IGFBP-3 gene expression was associated with poor 5-year overall survival compared with patients with low IGFBP-3 expression. Furthermore, IGFBP-3 gene expression was identified as an independent prognostic factor using multivariate analysis. Overexpression of the IGFBP-3 gene is considered an effective independent predictor of outcomes in patients with CRC.Entities:
Keywords: biomarker; colorectal cancer; insulin-like growth factor-1; insulin-like growth factor-1 receptor; insulin-like growth factor-2; insulin-like growth factor-binding protein-3; prognostic factor; survival
Year: 2017 PMID: 28521493 PMCID: PMC5431307 DOI: 10.3892/ol.2017.5936
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967