Manipulation of pulmonary prostacyclin synthase expression prevents murine lung cancer

Robert L. Keith, York E. Miller, Yasushi Hoshikawa, Mark D. Moore, Tracy L. Gesell, Bifeng Gao, Alvin M. Malkinson, Heiko A. Golpon, Raphael A. Nemenoff, Mark W. Geraci

研究成果: Article査読

116 被引用数 (Scopus)


Inhibition of cyclooxygenase (COX) activity decreases eicosanoid production and prevents lung cancer in animal models. Prostaglandin (PG) I2 (PGI2, prostacyclin) is a PGH2 metabolite with anti-inflammatory, antiproliferative, and antimetastatic properties. The instability of PGI2 has limited its evaluation in animal models of cancer. We hypothesized that pulmonary overexpression of prostacyclin synthase may prevent the development of murine lung tumors. Transgenic mice with selective pulmonary prostacyclin synthase overexpression were exposed to two distinct carcinogenesis protocols: an initiation/promotion model and a simple carcinogen model. The transgenic mice exhibited significantly reduced lung tumor multiplicity (tumor number) in proportion to transgene expression, a dose-response effect. Moreover, the highest expressing mice demonstrated reduced tumor incidence. To investigate the mechanism for protection, we evaluated PG levels and inflammatory responses. At the time of sacrifice following one carcinogenesis model, the transgenics exhibited only an increase in 6-keto-PGF, not a decrease in PGE2. Thus, elevated PGI2 levels and not decreased PGE2 levels appear to be necessary for the chemopreventive effects. When exposed to a single dose of butylated hydroxytoluene, transgenic mice exhibited a survival advantage; however, reduction in alveolar inflammatory response was not observed. These studies demonstrate that manipulation of PG metabolism downstream from COX produces even more profound lung cancer reduction than COX inhibition alone and could be the basis for new approaches to understanding the pathogenesis and prevention of lung cancer.

ジャーナルCancer Research
出版ステータスPublished - 01-02-2002

All Science Journal Classification (ASJC) codes

  • 腫瘍学
  • 癌研究


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