Dissimilar cytokine patterns in different human liver and colon cancer cell lines

被引:4
作者
Guerriero, Eliana [1 ]
Capone, Francesca [1 ]
Rusolo, Fabiola [1 ]
Colonna, Giovanni [2 ]
Castello, Giuseppe [1 ]
Costantini, Susan [1 ]
机构
[1] IRCCS, Ist Nazl Studio & Cura Tumori Fdn Giovanni Pascal, San Giovanni Rotondo, Italy
[2] Univ Naples 2, Dipartimento Biochim Biofis & Patol Gen, Naples, Italy
关键词
Cytokines; Chemokines; Growth factors; Multiplex immunoassay; Cancer cell lines; HUMAN HEPATOMA-CELLS; HEPATITIS-C VIRUS; INFLAMMATORY-BOWEL-DISEASE; HEPATOCELLULAR-CARCINOMA; COLORECTAL-CANCER; TUMOR PROGRESSION; EXPRESSION; CHEMOKINES; PATHOGENESIS; CIRRHOSIS;
D O I
10.1016/j.cyto.2013.09.002
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
An accurate and simultaneous estimate of cellular levels of a large cytokine number is very useful to obtain information about an organ dysfunction leading to cancer because through the understanding of the evolution of cytokine patterns we can recognize and predict the disease progression. Cancer cell lines are commonly used to study the cancer microenvironment, to analyze their chemosensitivity and carcinogenesis as well as to test in vitro the effect of molecules, such as drugs or anti-oxidants, on the inflammation status and its progression. We noted that various cell lines commonly used as a model for studies on liver and colon cancer possess different patterns of cytokines. This aspect may generate data not comparable in laboratories using different cell lines; thus, to investigate the origin of these abnormalities we compared the cell lines HepG2 and Huh7, and HT-29 and HCT-116, for liver and colon cancer, respectively. In this context we have evaluated and compared the levels of cytokines, chemokines and growth factors in the supernatants of these cellular lines. Our aim was to identify what cytokines were significantly different correlating similarities and differences to the specific inflammation status of each cellular model of cancer. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:584 / 589
页数:6
相关论文
共 54 条
[1]   The inflammatory micro-environment in tumor progression: The role of tumor-associated macrophages [J].
Allavena, Paola ;
Sica, Antonio ;
Solinas, Graziella ;
Porta, Chiara ;
Mantovani, Alberto .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2008, 66 (01) :1-9
[2]   Inflammation and cancer: back to Virchow? [J].
Balkwill, F ;
Mantovani, A .
LANCET, 2001, 357 (9255) :539-545
[3]   CHARACTERIZATION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 STRAINS RECOVERED FROM THE BOWEL OF INFECTED INDIVIDUALS [J].
BARNETT, SW ;
BARBOZA, A ;
WILCOX, CM ;
FORSMARK, CE ;
LEVY, JA .
VIROLOGY, 1991, 182 (02) :802-809
[4]   Simultaneous evaluation of the circulating levels of both Th1 and Th2 chemokines in patients with autoimmune Addison's disease [J].
Bellastella, G. ;
Rotondi, M. ;
Pane, E. ;
Costantini, S. ;
Colella, C. ;
Calemma, R. ;
Capone, F. ;
Falorni, A. ;
Castello, G. ;
Sinisi, A. A. ;
Bizzarro, A. ;
Chiovato, L. ;
Bellastella, A. ;
De Bellis, A. .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2011, 34 (11) :831-834
[5]   Serum cytokine levels in patients with hepatocellular carcinoma [J].
Capone, Francesca ;
Costantini, Susan ;
Guerriero, Eliana ;
Calemma, Rosa ;
Napolitano, Maria ;
Scala, Stefania ;
Izzo, Francesco ;
Castello, Giuseppe .
EUROPEAN CYTOKINE NETWORK, 2010, 21 (02) :99-104
[6]   Associated neoplastic disease in inflammatory bowel disease [J].
Cendan, Juan C. ;
Behms, Kevin E. .
SURGICAL CLINICS OF NORTH AMERICA, 2007, 87 (03) :659-+
[7]   Tumor-Derived Chemokine CCL5 Enhances TGF-β-Mediated Killing of CD8+ T Cells in Colon Cancer by T-Regulatory Cells [J].
Chang, Li-Yuan ;
Lin, Yung-Chang ;
Mahalingam, Jayashri ;
Huang, Ching-Tai ;
Chen, Ten-Wen ;
Kang, Chiao-Wen ;
Peng, Hui-Min ;
Chu, Yu-Yi ;
Chiang, Jy-Ming ;
Dutta, Avijit ;
Day, Yuan-Ji ;
Chen, Tse-Ching ;
Yeh, Chau-Ting ;
Lin, Chun-Yen .
CANCER RESEARCH, 2012, 72 (05) :1092-1102
[8]   Chemokine RANTES Promoter Dimorphisms and Hepatocellular Carcinoma Occurrence in Patients with Alcoholic or Hepatitis C Virus-Related Cirrhosis [J].
Charni, Faten ;
Sutton, Angela ;
Rufat, Pierre ;
Laguillier, Christelle ;
Mansouri, Abdellah ;
Moreau, Richard ;
Ganne-Carrie, Nathalie ;
Trinchet, Jean-Claude ;
Beaugrand, Michel ;
Charnaux, Nathalie ;
Nahon, Pierre .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2011, 20 (07) :1439-1446
[9]  
Choi J. W., 2013, PROTEOMICS
[10]   Treatment of monocytes with interleukin (IL)-12 plus IL-18 stimulates survival, differentiation and the production of CXC chemokine ligands (CXCL)8, CXCL9 and CXCL10 [J].
Coma, G. ;
Pena, R. ;
Blanco, J. ;
Rosell, A. ;
Borras, F. E. ;
Este, J. A. ;
Clotet, B. ;
Ruiz, L. ;
Parkhouse, R. M. E. ;
Bofill, M. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2006, 145 (03) :535-544