Title: Hematopoietic prostaglandin D synthase (HPGDS): a high stability, Val187Ile isoenzyme common among African Americans and its relationship to risk for colorectal cancer.

Authors: Tippin, Brigette L; Levine, A Joan; Materi, Alicia M; Song, Wen-Liang; Keku, Temitope O; Goodman, Julie E; Sansbury, Leah B; Das, Sudipto; Dai, Aihua; Kwong, Alan M; Lin, Amy M; Lin, John M; Park, Jae Man; Patterson, Ruth E; Chlebowski, Rowan T; Garavito, R Michael; Inoue, Tsuyoshi; Cho, Wonhwa; Lawson, John A; Kapoor, Shiv; Kolonel, Laurence N; Le Marchand, Loïc; Haile, Robert W; Sandler, Robert S; Lin, Henry J

Published In Prostaglandins Other Lipid Mediat, (2012 Jan)

Abstract: Intestinal tumors in Apc(Min/+) mice are suppressed by over-production of HPGDS, which is a glutathione transferase that forms prostaglandin D(2) (PGD(2)). We characterized naturally occurring HPGDS isoenzymes, to see if HPGDS variation is associated with human colorectal cancer risk. We used DNA heteroduplex analysis and sequencing to identify HPGDS variants among healthy individuals. HPGDS isoenzymes were produced in bacteria, and their catalytic activities were tested. To determine in vivo effects, we conducted pooled case-control analyses to assess whether there is an association of the isoenzyme with colorectal cancer. Roughly 8% of African Americans and 2% of Caucasians had a highly stable Val187lle isoenzyme (with isoleucine instead of valine at position 187). At 37°C, the wild-type enzyme lost 15% of its activity in 1h, whereas the Val187Ile form remained >95% active. At 50°C, the half life of native HPGDS was 9min, compared to 42 min for Val187Ile. The odds ratio for colorectal cancer among African Americans with Val187Ile was 1.10 (95% CI, 0.75-1.62; 533 cases, 795 controls). Thus, the Val187Ile HPGDS isoenzyme common among African Americans is not associated with colorectal cancer risk. Other approaches will be needed to establish a role for HPGDS in occurrence of human intestinal tumors, as indicated by a mouse model.

PubMed ID: 21821144

MeSH Terms: No MeSH terms associated with this publication