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 Review Article

COX2- Inhibitors and Their Role in Cancer Prevention and Treatment

Timothy Allen, MD, Ph.D*1, Giridhar M.N.V, MD,MBA1, Ghazaleh Shoja E Razavi MD2

1Global Allied Pharmaceutical, Center for Excellence in Research & Development, USA
2Dir. Clinical Development- Oncology and Respiratory, Global Allied Pharmaceutical, USA

*Corresponding author: Dr.Timothy Allen, MD, PhD, Global Allied Pharmaceutical, Center for Excellence in Research and Development, USA, Tel: 321-945-4283; Email: Timothy.Allen@gapsos.com

Submitted: 02-26-2015 Accepted: 05-23-2015  Published: 06-02-2015

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Article

 

Abstract

The various steps, in the process of carcinogenesis take many years, which contributes to several opportunities for intervention to inhibit growth of the disease. The reduction in the risk associated with cancer may be done by few effective chemopreventive agents through inhibition of the initiation of carcinoma or induction of apoptosis or DNA repair in cells harboring mutations. Over expression of cyclooxygenase-2(COX-2) has been identified in precancerous, cancerous and  metastatic human cancers and its level was found to be significantly correlating with cancer. In vitro, preclinical and clinical data have supported the hypothesis that COX-2 plays a central role in oncogenesis and treatment with COX-2 inhibitors provides an effective chemopreventive approach like activity of celecoxib in familial adenomatous polyposis. Understanding the role of COX-2 in initiation of carcinomas can lead to many clinical trials testing COX-2 inhibitors for the chemoprevention of a wide variety of cancers that over-express COX-2.

Keywords: COX-2; Prostaglandins; Tumorigenesis; COX-2 inhibitors; Chemoprevention

Abbreviations:

COX: Cyclooxygenase;
NSAIDs: Non Steroidal Anti-inflammatory Drugs;
DNA: Deoxyribonucleic Acid;
IL: Interleukin;
PG: Prostaglandin;
VEGF: Vascular endothelial growth factor ;
Bcl: B-cell lymphoma;
FAP: Familial Adenomatous Polyposis;
APC: Adenomatous Polyposis Coli ;
DCIS: Ductal carcinoma in situ;

Introduction

Cyclooxygenases are group of key enzymes involved in the synthesis of prostaglandin. Cyclooxygenase-2 (COX-2) is an inducible isoenzyme that plays a pivotal role as a mediator of inflammation. Cyclooxygenases catalyze the process of the conversion of arachidonic acid into prostaglandins [1-3]. Prostaglandins along with other arachidonic acid products such as thromboxane and 15-hydroxy-eicosatetraenoic acids belongs to the eicosanoid family of fatty acid molecules, which are known to regulate many physiological processes including the inflammatory response, immune responses like immunosuppressive effect [4-6], ovulation [7,8], and induction of mitosis in a cell [9,10]. Epidemiological studies showed that use of Non-Steroidal Anti-inflammatory Drugs (NSAIDs), which are prototypic inhibitors of COX, are associated with a reduced risk of various types of cancers [11].

Appropriately, growth and formation of tumor are also reduced on treatment with COX-2 inhibitors [12-18], COX-2 inhibitors causes fewer adverse effects as compared to traditional NSAIDs [19]. The improved safety profile of selective COX2 inhibitors makes it realistic to consider their long-term use in individuals from low to moderate risk of cancer. This review focuses on the rationale for using selective COX 2 inhibitors to prevent cancer.

Isoforms of cyclooxygensases (COX’s)

There are two isoforms of COX enzyme family COX-1 and COX-2. Cyclooxygenase-1 is a membrane-bound hemoglycoprotein that is constitutively expressed in the endoplasmic reticulum of cells in most healthy tissues and is responsible for local prostaglandin. On the other hand, COX-2, an inducible COX isoform, which is not usually detected in normal tissues [20,21]. It is only induced by proinflammatory and mitogenic stimuli and increases the synthesis of prostaglandins in inflamed and neoplastic tissues [22]. There are a number of structural differences between the COX-1 and COX-2 genes, such as differences in the cis elements within the promoter regions and 3´-untranslated domains.

The structure of the COX-2 gene indicates that it is an early gene product that occurs immediately during the inflammation [23,24]. Cyclooxygenase-2 synthesis is known as inducible and consider a variety of stimuli, such as interleukin-1 alpha and -1 beta, 25, 26 growth factors such as platelet-derived growth factor [27,28] epidermal growth factor, [29,30] and lipopolysaccharide and endothelial precursor [31,32] as in figure 1 [33].

Causative mechanism of COX 2 in cancer

COX 2 affects many important processes in carcinogenesis that makes it attractive therapeutic target. The various processes include xenobiotic metabolism, angiogenesis, apoptosis, immunosuppression and inflammation.

cancer fig 16.1
Figure 1. COX-2 is involved in the synthesis of prostaglandins that causes pain and inflammation in the body.

cancer fig 16.2.1
Figure 2. Representing the paradigm that expression of cyclooxygenase-2 (COX-2) and prostaglandin production which occurs during inflammation. Further, in the tumor environment COX-2/PG stimulate cell proliferation, cell survival and tumor angiogenesis; thus helps in promoting tumorigenesis [34].

Xenobiotic metabolism

The metabolism of Arachidonic acid by COX-2 produces mutagens which play a major role in carcinogenesis [35]. Malondialdehyde is a mutagen produced by isomerization of prostaglandin H2. It acts by forming adducts with deoxynucleotides, that causes frame-shifts and substitutions in base pair [36].

Wiese et. al., reported that peroxidase activity of cyclooxygenases catalyzes the formation of mutagens by the oxidation of aromatic amines, heterocyclic amines, and dihydrodiol derivatives of polycyclic hydrocarbons. Thus, overexpression of COX- 2 leads to DNA damage and carcinogenesis [37].

Angiogenesis

COX-2 has also been implicated in enhancing angiogenesis which plays a role in carcinogenesis. [38]. The growth of tumors depends on an increase in blood supply. Tumor cells ensure their own growth by secreting growth factors such as vascular endothelial growth factor (VEGF) that stimulate angiogenesis. Over expression of COX 2 in colon cancer cells increases the production of vascular growth factors, the migration of endothelial cells through a collagen matrix, and the formation of capillary-like networks in vitro [38]. These effects can be blocked by NS-398, a selective inhibitor of COX 2. Two recent studies also showed the importance of COX- 2 in angiogenesis [39].

Apoptosis

Tumorigenic potential of initiated cells can increase by the inhibition of apoptosis. Sheng et. al., [40] showed that prostaglandin E2 may inhibit apoptosis by inducing bcl-2 (B-cell lymphoma). Recently, it was found that Celecoxib (Celebrex), a selective COX-2 inhibitor, causes inhibition of COX-2, which results in a decrease production of prostaglandin E2, TBX 2 (Thromboxane), and increase apoptosis in vivo [41].

Inflammation and immunosuppression

Chronic inflammation increases the risk of cancer.42 Inflammation is associated with increased synthesis of prostaglandins partly through cytokine-mediated induction of COX-2. There is a link between chronic inflammation and carcinogenesis by the over expression of COX- 2. The growth of tumor is caused by the suppression of the immune system [43].

The tumor cells releases colony-stimulating factors which activate monocytes and macrophages for the synthesis of prostaglandin E2 (PGE2), and further causes inhibition in the production of immune regulatory lymphocytokines, proliferation of T-cell and B-cell, and the natural killer cells with its cytotoxic activity. Thus, selective inhibition of COX-2 promotes the antitumor activity by restoring the balance between IL-10 and IL-12 in vivo.

Therapeutic effects of COX-2 Inhibitors in various Cancers

NSAIDs act by inhibiting both COX 1 and COX 2 but primary anti-inflammatory mechanism is the inhibition of inducible isoform COX-2. The adverse effects of NSAIDs in the case of long term use are gastritis, gastrointestinal ulceration, and reversible liver and renal dysfunction [44- 46].

The over expression of COX-2 in humans has been studied in many cancer types and neoplastic precursor lesions as listed in the Table 1 below [47,48].

The data given above indicate that selective inhibition of COX-2 may contribute to be an effective strategy for preventing different types of cancers. The prevention of cancer implies multiple opportunities to inhibit the disease growth. The effective chemo preventive agents act by reducing the risk of cancer as well as by the prevention of the early and initiative stages of carcinoma through apoptosis and DNA repair in cell mutation or by preventing tumor growth during the progression stages of carcinogenesis [49]. The intervention in chemoprevention is possible at various stages of carcinogenesis starting from normal epithelium to invasive and metastatic cancer as in figure 2 [50].

Table 1. Neoplastic precursor lesions and types of cancer with the overexpression of COX-2.

cancer table 16.1

COX-2 Inhibitor Intervention

Normal epithelium Mild dysplasia Moderate dysplasia Invasive cancer Metastatic cancer

cancer fig 16.2

Figure 2. Process of carcinogenesis where chemoprevention intervention may be advantageous.

The proceeding clinical trials which evaluate the COX-2-specific inhibitors as chemoprevention and therapeutic agents are described in the following sections [50,51].

Colorectal Cancer

Colorectal cancer is the third leading cause of cancer death and a major health problem, with 2002 estimating 148,300 new cases and 56,000 deaths [52]. The majority of cases of colon carcinoma occur in patients who have no known susceptibility for the disease [53]. As per the estimates, currently American Cancer Society and Gastrointestinal Society colorectal cancer screening guidelines can lower the mortality rate upto 50% per annum [54].

Expression and Preclinical Data: COX-2

The chemo preventive effects of COX-2 inhibitors in the occurrence of colorectal cancer are the subject of intense study; animal models have been useful in investigating colorectal cancer pathogenesis.

A mutation in the Adenomatous Polyposis Coli (APC) gene results in spontaneous adenoma formation in the small intestine of APC delta716 knockout mice. Oshima and colleagues noticed that there is a cause-effect relationship between COX-2 overexpression and occurrence of gastrointestinal tumor by using the above rodent model [55]. It was shown that suppression of one allele of the COX-2 gene reduces the number of intestinal polyps by 66%, and suppression of both alleles results in a reduction of 86% [56] Further, treatment of COX-2-expressing azoxymethane-treated rats with oral Celecoxib suppressed formation of colorectal tumors by > 90%, compared with a suppression of 40% to 65% following administration of a COX inhibitor that is non selective [56,57].

Decreased occurrence of Colorectal Neoplasia

Long term use of NSAIDs causes reduction in the occurrence of colorectal adenomas, cancer and cancer mortality by 40% to 50% [58-60]. The vital study on Celecoxib for the treatment of Familial Adenomatous Polyposis (FAP) was done with 77 patients, who were randomized and given placebo or Celecoxib (100 or 400 mg twice daily) for 6 months [61]. The primary efficacy end point was the change in the number of colorectal adenomas (> 2 mm in size) at 6 months. There was a 4.5% reduction in the placebo-treated group11.9% reduction in the 100-mg Celecoxib-treated group and 28.0% reduction in the 400-mg Celecoxib-treated group. The decrease in incidence between the 400-mg Celecoxib twice-daily group and the placebo group was statistically significant (P = .003). The prevalence of adverse events was similar among the treatment groups and consisted primarily of rash, diarrhea, dyspepsia, fatigue, upper respiratory infection.

The positive results from the vital trial of Celecoxib in FAP support further investigation of COX-2 inhibitors for an overall chemoprevention strategy for colorectal tumors in other populations at risk, including patients with sporadic adenomatous polyps. There are several recently initiated clinical trials of Celecoxib in the prevention and recurrence of colorectal adenomas.

Non-melanomatous Skin Cancer

It is well-known fact that chronic sun exposure is a major cause of skin cancer .Up to the one million of new cases per year of Nonmelanomatous skin cancers such as basal cell carcinoma and squamous cell carcinoma were reported.62 Non melanomatous skin cancer is rare in young people. Its occurrence has been reported to increase with age and to be higher in men than woman [63]. A precursor lesion of squamous cell carcinoma is actinic keratoses with 60% of squamous cell carcinomas developing from it [64].

In Vitro and Preclinical Data: COX-2

In epidermis the balance between proliferation of cells (basal layer), cell differentiation (suprabasal, spinous and granular layers) and apoptosis (transitional zone) is closely regulated. The proliferative capacity is reduced when cells undergo terminal differentiation and leave the basal cell layer.

Neufang et. al. studied in a transgenic mouse model that the overexpression of COX-2 in epidermis results in epidermal differentiation [65]. Further, there was an increase in the proliferation of the epidermal cells and number of viable cornified layers.

In vitro study by Buckman et. al., demonstrated that exposure of human keratinocytes to UV-B causes a significant increase in prostaglandin E2 [66]. Indomethacin, a nonspecific COX inhibitor and SC58125, a COX-2 specific inhibitor acts individually by blocking UV-B induced COX-2 activity, in cultured keratinocytes of humans [67].

Clinical Data and Clinical Trials

An investigating report by Kagoura et al. showed that 4 of 16 basal cell carcinoma cases tested positive for COX-2 and 11 of 15 squamous cell carcinoma patients tested positive for COX-2 [68].

At University of Albama having sponsorship from the National Cancer institute, a phase IIB, double-blind, placebo-controlled trial is going on. The primary and secondary end point of this study are inducing actinic keratoses regression and effect of Celecoxib on potential surrogate end point biomarkers in actinic keratoses, sun-exposed skin, non-sun-exposed skin and their correlation with clinical outcome [69].

Prostate Cancer

It is the second leading cause of cancer death in men in the United States [70]. Treatment includes androgen ablation therapy, surgery, external beam radiation and radioactive seed implantation called as brachytherapy [71].

In vitro and Preclinical Data: COX-2

Lim et al. demonstrated the in vitro study of Sulindac, a COX-1 and COX-2 inhibitor has proapoptotic activity in prostate cancer cell lines like PC3, LNCaP, and PrEC. After 48 hrs of treatment with Sulindac, 50% of PC3 cells and 40% of LNCaP cells died [72].

The studies showing the effect of COX-2 inhibitors on angiogenesis in prostate carcinoma cell lines has been well established. This study explains that cell lines LNCaP, PC3 and PrEC were treated with two COX-2 inhibitors, Etodolac and NS398. It decreases the cell proliferation in carcinoma cell lines but not in the stromal cell lines of prostate [73].

Clinical Data and Clinical Trials

The overexpression of COX-2 is noted in 86% of prostate intraepithelial neoplasia lesions and 87% of carcinomas collected during prostatectomy as reported by Kirschenbaum et. Al [74]. In vivo results showed that there is decrease in micro vessel activity and angiogenesis by COX-2 inhibitor.

In preclinical experiment, activity of Exisulind (phosphodiesterase/ COX-1 and-2 inhibitor) is being evaluated in phase I/ II clinical trials which examines prostate-specific antigen response and disease response rate of Exisulind as a single agent or in combination with docetaxel [41-43].

Breast Cancer

There is variation in the occurrence of breast cancer with age and nationality. Major etiologies implicated in breast cancer are ovarian dysfunction and abnormal hormone production [75]. The common treatment modalities are surgery, radiation and chemotherapy or their combination [76].

In vitro and Preclinical Data: COX-2

Rozic et. al. reported the role of prostaglandins in the proliferation, migration, survival, angiogenic capacity and invasive behavior in murine mammary tumor cell line. Migratory and invasive behavior was done by an in vitro transwell migration assay. The COX-2 inhibitors blocked the migration and angiogenesis in in vivo. Thus, this study indicates that COX-2 inhibitors can be effective in preventing the development of this cancer [77].

In some studies, COX-2 inhibitors were note to act not only by preventing mammary carcinogenesis, but also by preventing multidrug resistance in breast cancer [78].

Gastric Cancer

There is variation in the occurrence of gastric cancer in different parts of the world and it is high in Japan and Chile and lowest in the Dominican Republic and Thailand [79]. The high rate of gastric cancer in Japan is due to the consumption of meat and fish.

Clinical Data: COX-2

Few studies explain that a Helicobacter pylori infection causes gastric cancer in a patient due to the overexpression of COX-2 [80]. There is also a direct relationship between COX-2 mRNA expressions and increased in tumor invasion. Due to this, COX- 2 inhibitors are effective in preventing H. pylori infection and other risk factors for gastric cancer. Further clinical trials are in pipeline for testing these agents.

Bladder Cancer

It is the fourth leading cause of cancer in men and eighth in women. In US, it is the ninth cause in men and 14th cause in women of death in cancer [81]. Majorly, it arises from bladder papilloma precursors, which provides opportunities to develop chemoprevention strategies [82].

In vitro and Preclinical Background: COX-2

The studies show that COX-2 inhibitors reduce the occurrence of bladder cancer caused by the chemical carcinogens [83]. Khan et. al. studied the expression of COX-1 and COX-2 in normal dogs and dogs with transitional cell carcinoma. It reveals the expression of COX-2 in carcinoma and in new blood vessels of tumor tissue but no differences in expression of COX-1between normal and malignant bladder was seen [84].

Clinical Data and Clinical Trials

At the University of Texas M. D. Anderson Cancer Center, Houston, a clinical trial on COX-2 inhibitors and incidence of bladder cancer is going on. (Table 2) [41-43]. It is designed for the comparison of time to recurrent treatment with Celecoxib or placebo in patients with high risk of superficial transitional cell carcinoma of bladder. It also correlates the modulation of biomarkers with bladder cancer.

Esophageal Cancer

There is a rapid increase in the occurrence of esophageal cancer in the patients with the premalignant condition known as Barrett’s esophagus which is due to replacement of normal squamous esophageal epithelium with a columnar type) [85,86]. The patients with Barrett’s esophagus have a high risk to esophageal adenocarcinoma by 30 to 40 fold [87].

In Vitro and Preclinical Background: COX-2

Li et. al., studied that aspirin decreases the cell growth in an esophageal cancer cell line [88]. The effect of COX-2 inhibitor NS398 on apoptosis and gene expression that regulate apoptosis were tested. In vitro, apoptosis is induced in esophageal cancer cell lines by COX-2 inhibitor through a cytochrome C-dependent pathway. Activation of caspase-9 and caspase-10 by NS398, and addition of a caspase inhibitor reverses the effect of apoptosis of COX-2 antagonist [88]. Therefore, these data refers that COX-2 inhibitors may be used for chemoprevention and treatment of esophageal cancer.

Clinical Data

Kandil et. al. studied the esophageal punch biopsy specimens in patients with Barrett’s esophagus [89]. COX-2 was found in Barrett’s esophagus tissue with or without dysplasia, indicating that COX-2 may play a role in the early stages of development of adenocarcinoma [90].

Currently a clinical study coordinated by the Johns Hopkins Comprehensive Cancer Center, Baltimore is going on to evaluate the efficacy and safety of Celecoxib in patients with Barrett’s esophagus.

The ongoing clinical trials which evaluate the COX-nonspecific and COX-2 specific inhibitors as chemoprevention and therapeutic agents which are discussed above are mentioned in the following Table 2.

COX- Cyclooxygenase, FAP- Familial adenomatous polyposis, DCIS- Ductal carcinoma in situ

cancer table 16.2

Table 2. Clinical trials of COX inhibitors in Cancer prevention and treatment [41- 43].

COX- Cyclooxygenase, FAP- Familial adenomatous polyposis, DCIS- Ductal carcinoma in situ

Conclusion

Cyclooxygenase is a natural enzyme that mediates inflammation and other immune responses. Over expression of COX-2 is noted in various malignancies associated with chronic inflammatory conditions. The available data indicate that COX2 inhibitors can stall the progression of carcinoma at various stages, especially in tumors that take origin form nonmalignant inflammatory precursors. COX 2 inhibitors has a role both in the treatment and prevention. Recent trials noted that COX 2 inhibitors such as Celecoxib have an important role in chemoprevention of gastrointestinal carcinomas such as colon cancer, FAP and colorectal polyps. Additionally, the safety profile of COX 2 inhibitors is noteworthy when compared to chemotherapeutic agents.

References

 References

1.Topley N, Petersen MM, Mackenzie R. Human peritoneal mesothelial cell prostaglandin synthesis: Induction of cyclooxygenase mRNA by peritoneal macrophage-derived cytokines. Kidney International. 1994, 46(3): 900-909.

2.Kulkarni PS. Synthesis of cyclooxygenase products by human anterior uvea from cyclic prostaglandin endoperoxide (PG H2). Experimental Eye Research. 1981, 32(2): 197-204.

3.Holmes DR, Wester W, Thompson RW. Prostaglandin E2 synthesis and cyclooxygenase expression in abdominal aortic aneurysms. Journal of Vascular Surgery. 1997, 25(5): 810-815.

4.Foster SJ, McCormick ME, Howarth A. The contribution of cyclooxygenase and lipoxygenase products to acute inflammation in the rat. Agents Actions. 1986, 17(3-4): 358-359.

5.Seibert K, Masferrer JL. Role of inducible cyclooxygenase (COX-2) in inflammation. Receptor. 1994, 4: 17-23.

6.Vane JR, Mitchell JA, Appleton I. Inducible isoforms of cyclooxygenase and nitric-oxide synthase in inflammation. Proceedings of the National Academy of Sciences, USA. 1994, 91(6): 2046-2050.

7.Joyce IM, Pendola FL, O’Brien M. Regulation of prostaglandin- endoperoxide synthase 2 messenger ribonucleic acid expression in mouse granulosa cells during ovulation. Endocrinology. 2001, 142(7): 3187-3197.

8.Matsumoto H, Ma W, Smalley W. Diversification of cyclooxygenase- 2-derived prostaglandins in ovulation and implantation. Biology of Reproduction. 2001, 64(5): 1557-1565.

9.Hwang D, Jang BC, Yu G. Expression of mitogen-inducible cyclooxygenase induced by lipopolysaccharide: Mediation through both mitogen-activated protein kinase and NF-kappa B signaling pathways in macrophages. Biochemical Pharmacology. 1997, 54(1): 87-96.

10.Kujubu DA, Herschman HR. Dexamethasone inhibits mitogen induction of the TIS10 prostaglandin synthase/cyclooxygenase gene. The Journal of Biological Chemistry. 1992, 267(12): 7991-7994..

11.Thun MJ. Nonsteroidal anti-inflammatory drugs as anticancer agents: mechanistic, pharmacologic, and clinical issues. Journal of the National Cancer Institute. 2003, 94(4): 252-266.

12.Oshima M. Suppression of intestinal polyposis in APCΔ716 knockout mice by inhibition of cyclooxygenase-2 (Cox 2). Cell. 1996, 87: 803–809.

13.Chulada PC. Genetic disruption of Ptgs-1, as well as Ptgs- 2, reduces intestinal tumorigenesis in Min mice. Cancer Research. 2000, 60: 4705-4708.

14.Tiano HF. Deficiency of either cyclooxygenase (COX)-1 or COX-2 alters epidermal differentiation and reduces mouse skin tumorigenesis. Cancer Research. 2002, 62: 3395–3401.

15.Jacoby RF. The cyclooxygenase-2inhibitor celecoxib is a potent preventive and therapeutic agent in the Min mouse model of adenomatous polyposis. Cancer Research. 2000, 80(18):5040–5044.

16.Oshima M. Chemoprevention of intestinal polyposis in APCΔ716 mouse by rofecoxib, a specific cyclooxygenase-2inhibitor. Cancer Research. 2001, 61: 1733–1740.

17.Harris RE. Chemoprevention of breast cancer in rats by celecoxib, a cyclooxygenase 2 inhibitor. Cancer Research. 2000, 60: 2101–2103.

18.Fischer SM. Chemopreventive activity of celecoxib, a specific cyclooxygenase-2 inhibitor, and indomethacin against ultraviolet light-induced skin carcinogenesis. Molecular Carcinogenesis. 1999, 25: 231-240.

19.Langman MJ, Jensen DM, Watson DJ. Adverse upper gastrointestinal effects of rofecoxib compared with NSAIDs. JAMA. 1999, 282: 1929 -1933.

20.Reed DW, Bradshaw WS, Xie W. In vivo and in vitro expression of a non mammalian cyclooxygenase-1. Prostaglandins. 1996, 52: 269-284.

21.Lipsky PE. Role of cyclooxygenase-1 and -2 in health and disease. The American Journal of Orthopedics. 1999, 28: 8-12.

22.Subbaramaiah K, Telang N and Ramonetti JT. Transcription ofcyclooxygenase-2 is enhanced in transformed mammary epithelial cells. Cancer Research. 1996, 56: 4424–4429.

23.Maier JA, Hla T, Maciag T. Cyclooxygenase is an immediate- early gene induced by interleukin-1 in human endothelial cells. The Journal of Biological Chemistry. 1990, 265: 10805- 10808.

24.Luckman SM, Dye S, Cox HJ. Induction of members of the Fos/Jun family of immediate-early genes in identified hypothalamic neurons: in vivo evidence for differential regulation. Neuroscience. 1996, 73: 473-485.

25.Hinterleitner TA, Saada JI, Berschneider HM. IL-1 stimulates intestinal myofibroblast COX gene expression and augments activation of Cl- secretion in T84 cells. American Journal of Physiology. 1996, 271: C1262-C1268.

26.Huang ZF, Massey JB, Via DP. Differential regulation of cyclooxygenase- 2 (COX-2) mRNA stability by interleukin-1 beta (IL-1 beta) and tumor necrosis factor-alpha (TNF-alpha) in human in vitro differentiated macrophages. Biochemical Pharmacology. 2000, 59: 187-194.

27.Gilroy DW, Saunders MA, Wu KK. COX-2 expression and cell-cycle progression in human fibroblasts. American Journal of Physiology. 2001, 281: C188-C194.

28.Goppelt-Struebe M, Rehm M, Schaefers HJ. Induction of cyclooxygenase- 2 by platelet-derived growth factor (PDGF) and its inhibition by dexamethasone are independent of NF-kappaB/ kappaB transcription factors. Naunyn Schmiedebergs Achieves of Pharmacology. 2000, 361: 636-645.

29.Goppelt-Struebe M, Wiedemann T, Heusinger-Ribeiro J. Cox-2 and osteopontin in co cultured platelets and mesangial cells: role of glucocorticoids. Kidney International. 2000, 57: 2229-2238.

30.Majima M, Isono M, Ikeda Y. Significant roles of inducible cyclooxygenase (COX)-2 in angiogenesis in rat sponge implants. The Japanese Journal of Pharmacology. 1997, 75: 105-114.

31.Shimada K, Kita T, Yonetani Y. Modulation by endothelin-1 of lipopolysaccharide-induced cyclooxygenase 2 expression in mouse peritoneal macrophages. European Journal of Pharmacology. 1999, 376: 285-292.

32.Shimada K, Kita T, Yonetani Y. The effect of endothelin-1 on lipopolysaccharide-induced cyclooxygenase 2 expression in association with prostaglandin E2. European Journal of Pharmacology. 2000, 388: 187-194.

33.Difference Between COX1 and COX2, by Dr khezar hayatin medical. 2013.>

34.Division of experimental oncology.

35.Plastaras JP, Guengerich FP and NebertDW. Xenobiotic metabolizing cytochrome P450 converts prostaglandin endoperoxide to hydroxyl heptadecatrienoic acid and the mutagen, malondialdehyde. Journal of Biological Chemistry. 2000, 275: 11784–11790.

36.Marnett LJ. Aspirin and the potential role of prostaglandins in colon cancer. Cancer Research. 1992, 52: 5575-5589.

37.Wiese FW, Thompson PA, Kadlubar FF. Carcinogen substrate specificity of human COX-1 and COX-2. Carcinogenesis. 2001, 22: 5-10.

38.Tsujii M, Kawano S and Tsuji S. Cyclooxygenase regulates angiogenesis induced by colon cancer cells. Cell. 1998, 93: 705–716.

39.Williams CS, Tsujii M and Reese J. Hostcyclooxygenase-2 modulates carcinoma growth. Journal of Clinical Investigation. 2000, 105: 1589–1594.

40.Sheng H, Shao J, Morrow JD. Modulation of apoptosis and bcl-2 expression by prostaglandin E2 in human colon cancer cells. Cancer Research. 1998, 58: 362-366.

41.Leahy K, Ornberg R, Wang Y. Cyclooxygenase-2 inhibition by celecoxib reduces proliferation and induces apoptosis in epithelial cells. Cancer Research. 2002, 62: 625-631.

42.Weitzman SA and Gordon LI. Inflammation and cancer: role of phagocyte-generated oxidants in carcinogenesis. Blood. 1990, 76: 655–663.

43.Balch CM, Dougherty PA and Cloud GA. Prostaglandin E2-mediated suppression of cellular immunity in colon cancer patients. Surgery.1984, 95: 71–77.

44.Whelton A. COX-1 sparing and COX-2 inhibitory drugs: The renal and hepatic safety and tolerability profiles of celecoxib. American Journal of Therapeutics. 2000, 7: 151-152.

45.Eschwege P, de Ledinghen V, Camilli T. Cyclooxygenases [in French]. La Presse Medicale. 2001, 30: 511-514.

46.Tanasescu S, Levesque H, Thuillez C. Pharmacology of aspirin [in French]. La Revue de Médecine Interne. 2000, 21(1): 18-26.

47.Soslow RA, Dannenberg AJ, Rush D. COX-2 is expressed in human pulmonary, colonic, and mammary tumors. Cancer. 2000, 89: 2637-2645.

48.Ochiai M, Oguri T, Isobe T. Cyclooxygenase-2 (COX-2) mRNA expression levels in normal lung tissues and non-small cell lung cancers. Japanese Journal of Cancer Research. 1999, 90: 1338-134.

49.Center Watch Clinical Trials Listing Service. Patient and general resources.

50.National Cancer Institute. PDQ® Clinical Trials Database User’s Guide.

51.Ryan CW, Stadler WM, Vogelzang NJ. Docetaxel and exisulind in hormone-refractory prostate cancer. Seminars in Oncology. 2001, 28: 56-61.

52.Jemal A, Thomas A, Murray T. Cancer statistics. A Cancer Journal for Clinicians. 2002, 52: 23-47.

53.Arguedas MR, Heudebert GR, Wilcox CM. Surveillance colonoscopy or chemoprevention with COX-2 inhibitors in average- risk post-polypectomy patients: A decision analysis. Alimentary Pharmacology and Therapeutics. 2001, 15: 631-638

54.Benson AB III, Desch CE, Flynn PJ. 2000 update of American Society of Clinical Oncology colorectal cancer surveillance guidelines. Journal of Clinical Oncology. 2000, 18(20): 3586- 3588.

55.Oshima M, Sugiyama H, Kitagawa K. APC gene messenger RNA: Novel isoforms that lack exon 7. Cancer Research. 1993, 53: 5589-5591.

56.Oshima M, Dinchuk JE, Kargman SL. Suppression of intestinal polyposis in APC delta716 knockout mice by inhibition of cyclooxygenase-2 (COX-2). Cell. 1996, 87: 803-809.

57.Reddy BS. Novel approaches to the prevention of colon cancer by nutritional manipulation and chemoprevention. The Fourth De Witt S. Goodman lecture. Cancer Epidemiological Biomarkers Prevention. 2000, 9: 239-247.

58.Thun MJ, Namboodiri MM, Calle EE. Aspirin use and risk of fatal cancer. Cancer Research. 1993, 53: 1322-1327.

59.Giovannucci E, Rimm EB, Stampfer MJ. Aspirin use and the risk for colorectal cancer and adenoma in male health professionals. Annals of Internal Medicine. 1994, 121: 241-246.

60.Giovannucci E, Egan KM, Hunter DJ. Aspirin and the risk of colorectal cancer in women. New England Journal of Medicine. 1995, 333: 609-614.

61.Steinbach G, Lynch PM, Phillips RK. The effect of celecoxib, a cyclooxygenase-2 inhibitor, in familial adenomatous polyposis. New England Journal of Medicine. 2000, 342: 1946-1952.

62.Marks R. The role of treatment of actinic keratoses in the prevention of morbidity and mortality due to squamous cell carcinoma. Archives of Dermatology. 1991, 127: 1031-1033.

63.Giles G.G., Marks R, Foley P. Incidence of nonmelanoma skin cancer treated in Australia. British Medical Journal. 1998, 296: 13-17.

64.Marks R, Rennie G, Selwood TS. Malignant transformation of solar keratoses to squamous cell carcinoma. Lancet. 1988, 1: 795-797.

65.Neufang G, Furstenberger G, Heidt M. Abnormal differentiation of epidermis in transgenic mice constitutively expressing cyclooxygenase-2 in skin. Proceedings of the National Academy of Sciences, U S A. 2001, 98: 7629-7634.

66.Buckman SY, Gresham A, Hale P. COX-2 expression is induced by UVB exposure in human skin: Implications for the development of skin cancer. Carcinogenesis. 1998, 19: 723-729.

67.Muller-Decker K, Kopp-Schneider A, Marks F. Localization of prostaglandin H synthase isoenzymes in murine epidermal tumors: Suppression of skin tumor promotion by inhibition of prostaglandin H synthase-2. Molecular Carcinogenesis. 1998, 23: 36-44.

68.Kagoura M, Toyoda M, Matsui C. Immuno histochemical expression of cyclooxygenase-2 in skin cancers. Journal of Cutaneous Pathology. 2001, 28: 298-302.

69.Hosomi Y, Yokose T, Hirose Y. Increased cyclooxygenase 2 (COX-2) expression occurs frequently in precursor lesions of human adenocarcinoma of the lung. Lung Cancer. 2000, 30: 73- 81.

70.Jemal A, Thomas A, Murray T. Cancer statistics. A Cancer Journal for Clinicians. 2002, 52: 23-47.

71.Sella A, Konichezky M, Flex D. Low PSA metastatic androgen- independent prostate cancer. European Urology. 2000, 38: 250-254.

72.Lim JT, Piazza GA, Han EK. Sulindac derivatives inhibit growth and induce apoptosis in human prostate cancer cell lines. Biochemical Pharmacology. 1999, 58: 1097-1107.

73.Kamijo T, Sato T, Nagatomi Y. Induction of apoptosis by cyclooxygenase- 2 inhibitors in prostate cancer cell lines. International Journal of Urology. 2001, 8: S35-S39.

74.Kirschenbaum A, Liotta DR, Yao S. Immuno histochemical localization of cyclooxygenase-1 and cyclooxygenase-2 in the human fetal and adult male reproductive tracts. Journal of Clinical Endocrinology and Metabolism. 2000, 85: 3436-3441.

75.Warren JL, Feuer E, Potosky AL. Use of Medicare hospital and physician data to assess breast cancer incidence. Medical Care. 1999, 37: 445-456.

76.Yonemoto RH. Breast cancer in Japan and United States: Epidemiology, hormone receptors, pathology, and survival. Achieves of Surgery. 1980, 115: 1056-1062.

77.Rozic JG, Chakraborty C, Lala PK. Cyclooxygenase inhibitors retard murine mammary tumor progression by reducing tumor cell migration, invasiveness and angiogenesis. International Journal of Cancer. 2001, 93: 497-506.

78.Ratnasinghe D, Phang JM, Yeh GC. Differential expression and activity of phosphatases and protein kinases in Adriamycin sensitive and resistant human breast cancer MCF-7 cells. International Journal of Oncology. 1998, 13: 79-84.

79.Pausawasdi A, Suntharabha S, Tanwatcharabhan P. Clinical study of gastric cancer. Journal of Medical Association of Thailand. 1980, 63: 655-661.

80.Uemura N, Okamoto S, Yamamoto S. Helicobacter pylori infection and the development of gastric cancer. New England Journal of Medicine. 2001, 345: 784-789.

81.Shaham J, Melzer A, Kaufman Z. Occupation and bladder cancer [in Hebrew]. Harefuah. 1996, 131: 382-386.

82.Mungan NA, Aben KK, Schoenberg MP. Gender differences in stage-adjusted bladder cancer survival. Urology. 2000, 55: 876-880.

83.Piazza GA, Thompson WJ, Pamukcu R. Exisulind, a novel proapoptotic drug, inhibits rat urinary bladder tumorigenesis. Cancer Research. 2001, 61: 3961-3968.

84.Khan KN, Knapp DW, Denicola DB. Expression of cyclooxygenase- 2 in transitional cell carcinoma of the urinary bladder in dogs. American Journal of Veterinary Research. 2000, 61: 478-481.

85.Dent J, Bremner CG, Collen MJ. Barrett’s oesophagus. Journal of Gastroenterology and Hepatology. 1991, 6: 1-22.

86.Spechler SJ. Pathogenesis and epidemiology of Barrett esophagus [in German]. Chirurg. 1994, 65: 84-87.

87.Eckardt VF, Kanzler G, Bernhard G. Life expectancy and cancer risk in patients with Barrett’s esophagus: A prospective controlled investigation. American Journal of Medicine. 2001,111: 33-37.

88.Li M, Wu X, Xu XC. Induction of apoptosis by cyclo-oxygenase- 2 inhibitor NS398 through a cytochrome C-dependent pathway in esophageal cancer cells. International Journal of Cancer. 2001, 93: 218-223.

89.Kandil HM, Tanner G, Smalley W. Cyclooxygenase-2 expression in Barrett’s esophagus. Digestive Diseases and Sciences. 2001, 46: 785-789.

90.Wilson KT, Fu S, Ramanujam KS. Increased expression of inducible nitric oxide synthase and cyclooxygenase-2 in Barrett’s esophagus and associated adenocarcinoma. Cancer Research. 1998, 58: 2929-2934.

Cite this article: Timothy A. COX-2 Inhibitors and Their Role in Cancer Prevention and Treatment. J J Cancer Sci Res. 2015, 1(3): 016.

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