Abstract
To develop an effective therapeutic approach to pancreatic ductal adenocarcinoma (PDAC), we focused on the antitumor mechanism of protein-bound polysaccharide (PSK) under hypoxia. PSK decreased proliferation in PDAC cells under hypoxia but not normoxia. PSK also showed anti-tumor effects in vivo, inhibited invasiveness of PDAC cells, and decreased the expression of HIF-1α and hedgehog (Hh) signaling-related molecules under hypoxia. Inhibition of HIF-1α and Hh signaling reduced proliferation and invasiveness in PDAC cells under hypoxia. In conclusion, we found new PSK-related pathways in invasiveness and proliferation in PDAC under hypoxia. PSK may be a promising therapeutic drug to treat refractory PDAC.
Original language | English |
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Pages (from-to) | 289-298 |
Number of pages | 10 |
Journal | Cancer Letters |
Volume | 335 |
Issue number | 2 |
DOIs | |
Publication status | Published - Jul 28 2013 |
All Science Journal Classification (ASJC) codes
- Oncology
- Cancer Research