TY - JOUR
T1 - Pre-clinical study of BK-UM, a novel inhibitor of HB-EGF, for ovarian cancer therapy
AU - Nam, Sung Ouk
AU - Yotsumoto, Fusanori
AU - Miyata, Kohei
AU - Suzaki, Yuki
AU - Yagi, Hiroshi
AU - Odawara, Takashi
AU - Manabe, Sadao
AU - Ishikawa, Toyokazu
AU - Kuroki, Masahide
AU - Mekada, Eisuke
AU - Miyamoto, Shingo
N1 - Publisher Copyright:
© 2014, International Institute of Anticancer Research. All rights reserved.
PY - 2014/8/1
Y1 - 2014/8/1
N2 - Background/Aim: Heparin-binding epidermal growth factor-like growth factor (HB-EGF), a member of the epidermal growth factor family, is a target for ovarian cancer therapy. The present study investigated the administration schedule of BK-UM, an anticancer agent targeting HB-EGF. Materials and Methods: The ovarian cancer cell line, RMG-I, was injected subcutaneously into five-week-old female nude mice. The BK-UM was administered intraperitoneally, using three administration schedules with different doses. The tumor volume was calculated every week. Statistical significance was assessed using the Mann-Whitney U-test. Results: At doses >0.1 mg/kg, BK-UM displayed significant antitumor effects, although the antitumor effects and body weights of mice did not significantly differ by dose or by three different administration schedules. At a dose <0.1 mg/kg, however, BK-UM had little inhibitory effect on tumor growth. Conclusion: Daily administration of BK-UM, which has a potentially dose-dependent antitumor effect, may be the optimal schedule for clinical application.
AB - Background/Aim: Heparin-binding epidermal growth factor-like growth factor (HB-EGF), a member of the epidermal growth factor family, is a target for ovarian cancer therapy. The present study investigated the administration schedule of BK-UM, an anticancer agent targeting HB-EGF. Materials and Methods: The ovarian cancer cell line, RMG-I, was injected subcutaneously into five-week-old female nude mice. The BK-UM was administered intraperitoneally, using three administration schedules with different doses. The tumor volume was calculated every week. Statistical significance was assessed using the Mann-Whitney U-test. Results: At doses >0.1 mg/kg, BK-UM displayed significant antitumor effects, although the antitumor effects and body weights of mice did not significantly differ by dose or by three different administration schedules. At a dose <0.1 mg/kg, however, BK-UM had little inhibitory effect on tumor growth. Conclusion: Daily administration of BK-UM, which has a potentially dose-dependent antitumor effect, may be the optimal schedule for clinical application.
UR - http://www.scopus.com/inward/record.url?scp=84908680641&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84908680641&partnerID=8YFLogxK
M3 - Article
C2 - 25075108
AN - SCOPUS:84908680641
SN - 0250-7005
VL - 34
SP - 4615
EP - 4620
JO - Anticancer research
JF - Anticancer research
IS - 8
ER -