Drug Currently in Phase III Trials for Arthritis Shows Tumor-Inhibiting Potential in Colon Cancer Model

Publication
Article
OncologyONCOLOGY Vol 12 No 3
Volume 12
Issue 3

Scientists at the American Health Foundation’s Nutritional Carcinogenesis Division, under the direction of Dr. Bandaru S. Reddy, division chief and associate director of the Foundation’s Naylor Dana Institute, Valhalla, New York, and Dr. Karen Seibert of Searle Research & Development, St. Louis, Missouri, described an exceptionally strong inhibitor of colon cancer development in an animal model assay in the February 1, 1998, issue of Cancer Research.

Scientists at the American Health Foundation’s Nutritional Carcinogenesis Division, under the direction of Dr. Bandaru S. Reddy, division chief and associate director of the Foundation’s Naylor Dana Institute, Valhalla, New York, and Dr. Karen Seibert of Searle Research & Development, St. Louis, Missouri, described an exceptionally strong inhibitor of colon cancer development in an animal model assay in the February 1, 1998, issue of Cancer Research.

Dietary administration of the cyclooxygenase-2 inhibitor celecoxib (SC-5 8635; 4-[5-(4-methylphenyl)-3-(trifluoromethyl)-IH-pyrazol-l-l]benzenesulfonamide) suppressed colon tumor incidence by 93% and multiplicity of colon tumors by 97% in a model assay in F344 rats that uses azoxymethane as the colon carcinogen.

Inhibition of Cyclooxygenase Enzyme
This study provides exciting evidence in support of the hypothesis that prostaglandin modulation, which is catalyzed by the cyclooxygenase enzymes (COX-1 and COX-2) in the arachidonic acid cascade, is involved in colon tumorigenesis and that blocking COX-2 activity leads to inhibition of tumor development. While COX- l is regarded as an enzyme that is expressed to generate prostaglandins during normal physiologic functions, the isozyme COX-2 can be induced by various agents, including growth factors and tumor promoters, and increased COX-2 expression has been measured in colon tumors.

The study showed that the specific inhibition of COX-2 by celecoxib affords chemopreventive strength beyond that seen in previous studies with nonsteroidal anti-inflammatory agents, such as aspirin. It further demonstrated that celecoxib has no toxic side effects (in the gastrointestinal tract or kidneys) like those seen with some of the nonsteroidal anti-inflammatory agents on the basis of inhibition of the constitutive enzyme COX-l.

Celecoxib is currently in phase III clinical trials for the treatment of arthritis. Further preclinical testing of celecoxib as an anticancer agent is scheduled, and researchers hope that these tests will lead to clinical trials in humans for confirmation of the chemopreventive potential of this promising agent against colon cancer in humans.

Recent Videos
As patients are nearing the end of life, different management strategies, such as opioids, may be needed to help mitigate pain or fatigue.
Kelley A. Rone, DNP, RN, AGNP-c, highlights the importance of having end-of-life discussions early in a patient’s cancer treatment course.
Alessio Pigazzi, MD, PhD, FACS, FASCRS, provides advice for upcoming surgeons starting out in the colorectal cancer field.
Alessio Pigazzi, MD, PhD, FACS, FASCRS, discussed how robot-assisted surgery for colorectal cancers has evolved over the past 20 years.
Alessio Pigazzi, MD, PhD, FACS, FASCRS, discussed surgical and medical oncology developments in the colorectal cancer field.
4 KOLs are featured in this panel.
4 KOLs are featured in this panel.
4 KOLs are featured in this panel.
Stacey A. Cohen, MD, and Daniel H. Ahn, DO, presenting slides
Stacey A. Cohen, MD, and Daniel H. Ahn, DO, presenting slides
Related Content