Celecoxib reduces fluidity and decreases metastatic potential of colon cancer cell lines irrespective of COX-2 expression

被引:32
|
作者
Sade, Asli [1 ]
Tuncay, Seda [1 ]
Cimen, Ismail [1 ]
Severcan, Feride [1 ]
Banerjee, Sreeparna [1 ]
机构
[1] Middle E Tech Univ, Dept Biol Sci, TR-06531 Ankara, Turkey
关键词
attenuated total reflectance-Fourier transform IR (ATR-FTIR); celecoxib (CLX); colon cancer; csyclo-oxygenase-2 (COX-2); electron spin resonance (ESR); fluidity; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; FAMILIAL ADENOMATOUS POLYPOSIS; ELECTRON-SPIN-RESONANCE; NF-KAPPA-B; MEMBRANE-FLUIDITY; INFRARED-SPECTROSCOPY; BREAST-CANCER; CYCLOOXYGENASE-2; INHIBITOR; ALPHA-TOCOPHEROL; MODEL MEMBRANES;
D O I
10.1042/BSR20100149
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
CLX (celecoxib), a selective COX-2 (cyclo-oxygenase-2) inhibitor, has numerous pleiotropic effects on the body that may be independent of its COX-2 inhibitory activity. The cancer chemopreventive ability of CLX, particularly in CRC (colorectal cancer), has been shown in epidemiological studies. Here we have, for the first time, examined the biophysical effects of CLX on the cellular membranes of COX-2 expressing (HT29) and COX-2 non-expressing (SW620) cell lines using ATR-FTIR (attenuated total reflectance Fourier transform IR) spectroscopy and SL-ESR (spin label-ESR) spectroscopy. Our results show that CLX treatment decreased lipid fluidity in the cancer cell lines irrespective of COX-2 expression status. As metastatic cells have higher membrane fluidity, we examined the effect of CLX on the metastatic potential of these cells. The CLX treatment efficiently decreased the proliferation, anchorage-independent growth, ability to close a scratch wound and migration and invasion of the CRC cell lines through Matrigel. We propose that one of the ways by which CLX exerts its anti-tumorigenic effects is via alterations in cellular membrane fluidity which has a notable impact on the cells' metastatic potential.
引用
收藏
页码:35 / 44
页数:10
相关论文
共 50 条
  • [1] Interaction between celecoxib and docetaxel or cisplatin in human cell lines of ovarian cancer and colon cancer is independent of COX-2 expression levels
    Bijman, Marcel N. A.
    Hermelink, Cristian A.
    van Berkel, Maria P. A.
    Laan, Adrie C.
    Janmaat, Maarten L.
    Peters, Godefridus J.
    Boven, Epie
    BIOCHEMICAL PHARMACOLOGY, 2008, 75 (02) : 427 - 437
  • [2] Transcriptional regulation of the COX-2 expression by nitric oxide in colon cancer cell lines
    Liu, Qiang
    Inoue, Hiroyasu
    Mahendran, Ratha
    ONCOLOGY REPORTS, 2008, 19 (01) : 269 - 274
  • [3] Overexpression of COX-2 in Celecoxib-Resistant Breast Cancer Cell Lines
    Singh, Balraj
    Irving, LaTashia R.
    Tai, Karen
    Lucci, Anthony
    JOURNAL OF SURGICAL RESEARCH, 2010, 163 (02) : 235 - 243
  • [4] Inhibition of COX-2 in colon cancer cell lines by celecoxib increases the nuclear localization of active p53
    Swamy, MV
    Herzog, CR
    Rao, CV
    CANCER RESEARCH, 2003, 63 (17) : 5239 - 5242
  • [5] COX-2 independent induction of cell cycle arrest and apoptosis in colon cancer cells by the selective COX-2 inhibitor celecoxib
    Grösch, S
    Tegeder, I
    Niederberger, E
    Bräutigam, L
    Geisslinger, G
    FASEB JOURNAL, 2001, 15 (12): : 2742 - +
  • [6] Antiproliferative effects of COX-2 inhibitor celecoxib on human breast cancer cell lines
    Bocca, Claudia
    Bozzo, Francesca
    Bassignana, Andrea
    Miglietta, Antonella
    MOLECULAR AND CELLULAR BIOCHEMISTRY, 2011, 350 (1-2) : 59 - 70
  • [7] Antiproliferative effects of COX-2 inhibitor celecoxib on human breast cancer cell lines
    Claudia Bocca
    Francesca Bozzo
    Andrea Bassignana
    Antonella Miglietta
    Molecular and Cellular Biochemistry, 2011, 350 : 59 - 70
  • [8] Selective COX-2 inhibitor (celecoxib) decreases cellular growth in prostate cancer cell lines independent of p53
    Katkoori, V. R.
    Manne, K.
    Vital-Reyes, V. S.
    Rodriguez-Burford, C.
    Shanmugam, C.
    Sthanam, M.
    Manne, U.
    Chatla, C.
    Abdulkadir, S. A.
    Grizzle, W. E.
    BIOTECHNIC & HISTOCHEMISTRY, 2013, 88 (01) : 38 - 46
  • [9] COX-2 over-expression and sensitivity to celecoxib and capecitabine in metastatic breast cancer patients
    Metro, G.
    Melucci, E.
    Sperdta, I
    Mottolese, M.
    Papoldo, P.
    Milella, M.
    Carlini, P.
    Ferretti, G.
    Cognetti, F.
    Fabi, A.
    BREAST CANCER RESEARCH AND TREATMENT, 2007, 106 : S169 - S170
  • [10] COX-2 and colon cancer: Potential targets for chemoprevention
    Fournier, DB
    Gordon, GB
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2000, : 97 - 102