抄録
Several studies have shown that cell fate regulation during embryonic development and oncogenic transformation share common regulatory mechanisms and signaling pathways. Indeed, an embryonic gene member of the EGF-Cripto-1/FRL1/ Cryptic family, Cripto-1, has been implicated in embryogenesis and in carcinogenesis. Cripto-1 together with the TGF- ligand Nodal is a key regulator of embryonic development and is a marker of undifferentiated human and mouse embryonic stem cells. While Cripto-1 expression is very low in normal adult tissues, Cripto-1 is re-expressed at high levels in several different human tumors, modulating cancer cell proliferation, migration, epithelial-to- mesenchymal transition and stimulating tumor angiogenesis. Therefore, inhibition of Cripto-1 expression using blocking antibodies or antisense expression vectors might be a useful modality not only to target fully differentiated cancer cells but also to target a subpopulation of tumor cells with stem-like characteristics.
| 本文言語 | 英語 |
|---|---|
| ページ(範囲) | 1127-1142 |
| ページ数 | 16 |
| ジャーナル | Future Oncology |
| 巻 | 6 |
| 号 | 7 |
| DOI | |
| 出版ステータス | 出版済み - 07-2010 |
| 外部発表 | はい |
UN SDG
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All Science Journal Classification (ASJC) codes
- 腫瘍学
- 癌研究
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