Reference - Detail
| RRC ID | 44637 |
|---|---|
| Author | Adachi Y, Ohashi H, Imsumran A, Yamamoto H, Matsunaga Y, Taniguchi H, Nosho K, Suzuki H, Sasaki Y, Arimura Y, Carbone DP, Imai K, Shinomura Y. |
| Title | The effect of IGF-I receptor blockade for human esophageal squamous cell carcinoma and adenocarcinoma. |
| Journal | Tumour Biol |
| Abstract |
Insulin-like growth factor-I receptor (IGF-IR) signaling is required for carcinogenicity and tumor development, and this pathway has not been well studied in human esophageal carcinomas. Esophageal cancer is one of the human cancers with the worst prognosis and has two main histologies: squamous cell carcinomas (ESCC) and adenocarcinoma (EAC). Previously, we have reported that detection of the IGF axis may be useful for the prediction of recurrence and poor prognosis of ESCC. We have also shown the successful therapy for several gastrointestinal cancers using recombinant adenoviruses expressing dominant negative IGF-IR (ad-IGF-IR/dn). The aim of this study is to develop potential targeted therapeutics to IGF-IR and to assess the effect of IGF-IR blockade in both of these types of esophageal cancer. We determined immunohistochemical expression of IGF-IR in a tissue microarray. We then assessed the effect of IGF-IR blockade on signal transduction, proliferation, apoptosis, and motility. Ad-IGF-IR/dn, a tyrosine kinase inhibitor, BMS-536924, and adenovirus expressing shRNA for IGF-IR were used. IGF-IR expression was common in both tumor types but not in normal tissues. IGF-IR was detected in metastatic sites at similar levels compared to the primary site. IGF-IR inhibition suppressed proliferation and colony formation in both cancers. IGF-IR blockades up-regulated both stress- and chemotherapy-induced apoptosis and reduced migration. Although IGF-IR/dn blocked ligand-induced activation of Akt-1 mainly, BMS-536924 effectively blocked both activation of Akt and MAPK. The IGF axis might play a key role in tumor progression of esophageal carcinomas. The IGF-IR targeting strategies might thus be useful anticancer therapeutics for human esophageal malignancies. |
| Volume | 35(2) |
| Pages | 973-85 |
| Published | 2014-2-1 |
| DOI | 10.1007/s13277-013-1131-2 |
| PMID | 24026884 |
| MeSH | Adenocarcinoma / genetics* Adenocarcinoma / pathology Adenocarcinoma / therapy Adenoviridae Carcinogenesis Carcinoma, Squamous Cell / genetics* Carcinoma, Squamous Cell / pathology Carcinoma, Squamous Cell / therapy Cell Line, Tumor Esophageal Neoplasms / genetics* Esophageal Neoplasms / pathology Esophageal Neoplasms / therapy Esophageal Squamous Cell Carcinoma Gene Expression Regulation, Neoplastic Humans Insulin-Like Growth Factor I / antagonists & inhibitors Insulin-Like Growth Factor I / biosynthesis Insulin-Like Growth Factor I / genetics* Molecular Targeted Therapy* Prognosis Receptor, IGF Type 1 / biosynthesis Receptor, IGF Type 1 / genetics* Signal Transduction / genetics |
| IF | 3.65 |
| Times Cited | 13 |
| WOS Category | ONCOLOGY |
| Altmetric score |
オルトメトリクス指標項目
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| The most frequently cited source | Patent(IFI CLAIMS) |
| Total number of mentions | 1 |
| Altmetric score changes over past 6months | 0.0 |
| Resource | |
| Human and Animal Cells | TE-1(RCB1894) TE-8(RCB2098) |