PMID- 23251235 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240109 IS - 1792-0981 (Print) IS - 1792-1015 (Electronic) IS - 1792-0981 (Linking) VI - 5 IP - 1 DP - 2013 Jan TI - Oral administration of monogalactosyl diacylglycerol from spinach inhibits colon tumor growth in mice. PG - 17-22 AB - Previously, we observed that purified monogalactosyl diacylglycerol (MGDG), a major glycoglycerolipid from spinach, selectively inhibits the activities of mammalian replicative DNA polymerases (alpha, delta and epsilon). However, the function of MGDG following ingestion is not well-known. In the present study, spinach MGDG suppressed the proliferation of Colon26 mouse colon cancer cells with an LD(50) of 24 mug/ml in vitro. gamma-cyclodextrin (CD)-MGDG complex was prepared and administered orally following Colon26 mouse tumor adhesion for 26 days. It was observed that 20 mg/kg equivalent (eq.) of the CD-MGDG complex reduced tumor volume by approximately 60% compared with that of the vehicle-treated controls. In immunohistochemical analysis, the CD-MGDG complex group showed a decreased number of proliferating cell nuclear antigen (PCNA)-positive cells and reduction of mitosis in the tumor cells compared with the control group. In addition, the CD-MGDG complex increased the number of terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL)-positive apoptotic cells and inhibited CD31-positive tumor blood vessel growth significantly. These results suggest that MGDG has the potential for cancer prevention and health promotion. FAU - Maeda, Naoki AU - Maeda N AD - Laboratory of Food and Nutritional Sciences, Department of Nutritional Science, Kobe-Gakuin University, Kobe, Hyogo 651-2180; FAU - Kokai, Yasuo AU - Kokai Y FAU - Hada, Takahiko AU - Hada T FAU - Yoshida, Hiromi AU - Yoshida H FAU - Mizushina, Yoshiyuki AU - Mizushina Y LA - eng PT - Journal Article DEP - 20121101 PL - Greece TA - Exp Ther Med JT - Experimental and therapeutic medicine JID - 101531947 PMC - PMC3524182 EDAT- 2012/12/20 06:00 MHDA- 2012/12/20 06:01 PMCR- 2012/11/01 CRDT- 2012/12/20 06:00 PHST- 2012/06/02 00:00 [received] PHST- 2012/10/02 00:00 [accepted] PHST- 2012/12/20 06:00 [entrez] PHST- 2012/12/20 06:00 [pubmed] PHST- 2012/12/20 06:01 [medline] PHST- 2012/11/01 00:00 [pmc-release] AID - etm-05-01-0017 [pii] AID - 10.3892/etm.2012.792 [doi] PST - ppublish SO - Exp Ther Med. 2013 Jan;5(1):17-22. doi: 10.3892/etm.2012.792. Epub 2012 Nov 1.