Format

Send to

Choose Destination
J Cell Physiol. 2019 Mar 20. doi: 10.1002/jcp.28483. [Epub ahead of print]

Increased IGF2BP3 expression promotes the aggressive phenotypes of colorectal cancer cells in vitro and vivo.

Xu W1,2, Sheng Y3, Guo Y1,2, Huang Z1,2, Huang Y1,2, Wen D1,2, Liu CY1,2, Cui L1,2, Yang Y4, Du P1,2.

Author information

1
Department of Colorectal Surgery, Xin-Hua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
2
Shanghai Colorectal Cancer Research Center, Shanghai, China.
3
State Key Laboratory of Oncogenes and Related Genes, Renji-Med-X Stem Cell, Research Center, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
4
Center for Systems Medicine, Suzhou Institute of Systems Medicine, Chinese Academy of Medical Sciences, Suzhou, China.

Abstract

Previous literatures reported insulin-like growth factor-2 messenger RNA-binding protein 3 (IGF2BP3) is a poor prognostic marker for colorectal cancer (CRC) patients. However, basic research on the effect and biological role of IGF2BP3 in CRC was still scare. Real-time quantitative polymerase chain reaction and western blot analysis were used to examine IGF2BP3 expression level in tumors and paired normal tissues from CRC patients. Tissue microarrays with 192 CRC patients were subjected to immunohistochemical staining to analyze the prognostic value of IGF2BP3. Proliferation assays, migration assays, and xenograft tumor formation in nude mice were performed to assess the biological role of IGF2BP3 in CRC cells. IGF2BP3 expression was significantly upregulated in tumor tissues compared with the matched normal tissues both in messenger RNA and protein level and was associated with worse prognosis. IGF2BP3 knockdown made cell cycle arrest to impair the proliferation ability of CRC cells and further inhibited the xenograft tumor growth in nude mice, also inhibited the migration ability of CRC cells via inducing epithelial-mesenchymal transition. Therefore, the research demonstrated that increased IGF2BP3 expression promoted the aggressive phenotypes of CRC cells. Targeted IGF2BP3 could be a novel and effective gene therapy for CRC patients to make a better prognosis.

KEYWORDS:

IGF2BP3; colorectal cancer; migration; prognosis; proliferation

PMID:
30895618
DOI:
10.1002/jcp.28483

Supplemental Content

Full text links

Icon for Wiley
Loading ...
Support Center