Celecoxib and fish oil: a combination strategy for decreased inflammatory mediators in early stages of experimental mammary cancer

被引:8
作者
Negi, Anjana Kumari [1 ]
Renuka [1 ]
Bhatnagar, Archana [1 ]
Agnihotri, Navneet [1 ]
机构
[1] Panjab Univ, Dept Biochem, Chandigarh 160014, India
关键词
Inflammation; Cytokine; Interleukins; NF-kappa B; COX-2; NF-KAPPA-B; BREAST-CANCER; UP-REGULATION; CYCLOOXYGENASE-2; INHIBITOR; TRANSCRIPTION FACTOR; DOWN-REGULATION; CHEMOPREVENTIVE ACTION; SERUM INTERLEUKIN-10; INCREASED EXPRESSION; COX-2; EXPRESSION;
D O I
10.1007/s10787-015-0259-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chronic inflammation has been directly linked to cancer progression. Therefore, current study was designed to understand the mechanism of action of chemopreventive effect of celecoxib and fish oil on inflammatory mediators in experimental mammary carcinoma. Female Wistar rats were distributed into control and DMBA treated groups and further subdivided based on pretreatment with celecoxib and/or fish oil. Inflammation was measured by assessing expression of NF-kappa B, COX-2 and cytokines. The results indicated an elevation in expression of NF-kappa B, COX-2 and cytokines' levels (IFN-gamma, IL-4 and IL-10) in DMBA group as compared to controls. On pretreatment with celecoxib and/or fish oil in DMBA treated animals, a significant reduction in expression of NF-kappa B, COX-2 and cytokines' levels was observed. The decrease was more pronounced with combinatorial regimen than either celecoxib or fish oil alone. To conclude, a combinatorial strategy of celecoxib and fish oil may generate an immune response against the tumor cell by altering cytokine repertoire and decrease the tendency of tumor cells to escape immune surveillance.
引用
收藏
页码:11 / 22
页数:12
相关论文
共 93 条
[61]   COX-2 inhibits fas-mediated apoptosis in cholangiocarcinoma cells [J].
Nzeako, UC ;
Guicciardi, ME ;
Yoon, JH ;
Bronk, SF ;
Gores, GY .
HEPATOLOGY, 2002, 35 (03) :552-559
[62]   20(S)-protopanaxatriol, one of ginsenoside metabolites, inhibits inducible nitric oxide synthase and cyclooxygenase-2 expressions through inactivation of nuclear factor-κB in RAW 264.7 macrophages stimulated with lipopolysaccharide [J].
Oh, GS ;
Pae, HO ;
Choi, BM ;
Seo, EA ;
Kim, DH ;
Shin, MK ;
Kim, JD ;
Kim, JB ;
Chung, HT .
CANCER LETTERS, 2004, 205 (01) :23-29
[63]   The duplicitous effects of interleukin 4 on tumour immunity: how can the same cytokine improve or impair control of tumour growth? [J].
Olver, S. ;
Apte, S. ;
Baz, A. ;
Kienzle, N. .
TISSUE ANTIGENS, 2007, 69 (04) :293-298
[64]   Myeloid-Derived Suppressor Cells: Linking Inflammation and Cancer [J].
Ostrand-Rosenberg, Suzanne ;
Sinha, Pratima .
JOURNAL OF IMMUNOLOGY, 2009, 182 (08) :4499-4506
[65]   NF-κB and cancer: how intimate is this relationship [J].
Prasad, Sahdeo ;
Ravindran, Jayaraj ;
Aggarwal, Bharat B. .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2010, 336 (1-2) :25-37
[66]   eInterleukin-4 enhances proliferation of human pancreatic cancer cells: evidence for autocrine and paracrine actions [J].
Prokopchuk, O ;
Liu, Y ;
Henne-Bruns, D ;
Kornmann, M .
BRITISH JOURNAL OF CANCER, 2005, 92 (05) :921-928
[67]   Regulation of death receptor expression and TRAIL/Apo2L-induced apoptosis by NF-κB [J].
Ravi, R ;
Bedi, GC ;
Engstrom, LW ;
Zeng, QW ;
Mookerjee, B ;
Gélinas, C ;
Fuchs, EJ ;
Bedi, A .
NATURE CELL BIOLOGY, 2001, 3 (04) :409-416
[68]   Aberrant rel/nfkb genes and activity in human cancer [J].
Rayet, B ;
Gélinas, C .
ONCOGENE, 1999, 18 (49) :6938-6947
[69]   A randomised feasibility study of EPA and Cox-2 inhibitor (Celebrex) versus EPA, Cox-2 inhibitor (Celebrex), Resistance Training followed by ingestion of essential amino acids high in leucine in NSCLC cachectic patients - ACCeRT Study [J].
Rogers, Elaine S. ;
MacLeod, Roderick D. ;
Stewart, Joanna ;
Bird, Stephen P. ;
Keogh, Justin W. L. .
BMC CANCER, 2011, 11
[70]  
Sasaki N, 2001, CLIN CANCER RES, V7, P4136