Changes in plasma chemokine C-C motif ligand 2 levels during treatment with eicosapentaenoic acid predict outcome in patients undergoing surgery for colorectal cancer liver metastasis
The mechanism of the anti-colorectal cancer (CRC) activity of the omega-3 fatty acid eicosapentaenoic acid (EPA) is not understood. We tested the hypothesis that EPA reduces expression of chemokine C-C motif ligand 2 (CCL2), a pro-inflammatory chemokine with known roles in metastasis.We measured CCL...
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Published in | Oncotarget Vol. 7; no. 19; pp. 28139 - 28150 |
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Abstract | The mechanism of the anti-colorectal cancer (CRC) activity of the omega-3 fatty acid eicosapentaenoic acid (EPA) is not understood. We tested the hypothesis that EPA reduces expression of chemokine C-C motif ligand 2 (CCL2), a pro-inflammatory chemokine with known roles in metastasis.We measured CCL2 in clinical samples from a randomized trial of EPA in patients undergoing liver surgery for CRC liver metastasis (LM) and preclinical models. Genome-wide transcriptional profiling of tumors from EPA-treated patients was performed.EPA decreased CCL2 synthesis by CRC cells in a dose-dependent manner. CCL2 was localized to malignant epithelial cells in human CRCLM. EPA did not reduce CCL2 content in human or mouse tumors compare to control. However, EPA treatment was associated with decreased plasma CCL2 levels compared with controls (P=0.04). Reduction in plasma CCL2 following EPA treatment predicted improved disease-free survival (HR 0.32; P=0.003). Lack of 'CCL2 response' was associated with a specific CRCLM gene expression signature.In conclusion, reduction in plasma CCL2 in patients with CRCLM treated with EPA predicts better clinical outcome and a specific tumor gene expression profile. Further work is needed to validate CCL2 as a therapeutic response biomarker for omega-3 fatty acid treatment of CRC patients. |
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AbstractList | The mechanism of the anti-colorectal cancer (CRC) activity of the omega-3 fatty acid eicosapentaenoic acid (EPA) is not understood. We tested the hypothesis that EPA reduces expression of chemokine C-C motif ligand 2 (CCL2), a pro-inflammatory chemokine with known roles in metastasis.We measured CCL2 in clinical samples from a randomized trial of EPA in patients undergoing liver surgery for CRC liver metastasis (LM) and preclinical models. Genome-wide transcriptional profiling of tumors from EPA-treated patients was performed.EPA decreased CCL2 synthesis by CRC cells in a dose-dependent manner. CCL2 was localized to malignant epithelial cells in human CRCLM. EPA did not reduce CCL2 content in human or mouse tumors compare to control. However, EPA treatment was associated with decreased plasma CCL2 levels compared with controls (P=0.04). Reduction in plasma CCL2 following EPA treatment predicted improved disease-free survival (HR 0.32; P=0.003). Lack of 'CCL2 response' was associated with a specific CRCLM gene expression signature.In conclusion, reduction in plasma CCL2 in patients with CRCLM treated with EPA predicts better clinical outcome and a specific tumor gene expression profile. Further work is needed to validate CCL2 as a therapeutic response biomarker for omega-3 fatty acid treatment of CRC patients. The mechanism of the anti-colorectal cancer (CRC) activity of the omega-3 fatty acid eicosapentaenoic acid (EPA) is not understood. We tested the hypothesis that EPA reduces expression of chemokine C-C motif ligand 2 (CCL2), a pro-inflammatory chemokine with known roles in metastasis. We measured CCL2 in clinical samples from a randomized trial of EPA in patients undergoing liver surgery for CRC liver metastasis (LM) and preclinical models. Genome-wide transcriptional profiling of tumors from EPA-treated patients was performed. EPA decreased CCL2 synthesis by CRC cells in a dose-dependent manner. CCL2 was localized to malignant epithelial cells in human CRCLM. EPA did not reduce CCL2 content in human or mouse tumors compare to control. However, EPA treatment was associated with decreased plasma CCL2 levels compared with controls (P=0.04). Reduction in plasma CCL2 following EPA treatment predicted improved disease-free survival (HR 0.32; P=0.003). Lack of ‘CCL2 response’ was associated with a specific CRCLM gene expression signature. In conclusion, reduction in plasma CCL2 in patients with CRCLM treated with EPA predicts better clinical outcome and a specific tumor gene expression profile. Further work is needed to validate CCL2 as a therapeutic response biomarker for omega-3 fatty acid treatment of CRC patients. |
Author | Cockbain, Andrew J Randerson-Moor, Juliette Burghel, Heather Coletta, P Louise Volpato, Milene Hull, Mark A Perry, Sarah L Ingram, Nicola Lowes, David Droop, Alastair Mann, Jake Wilson, Erica Marston, Gemma |
AuthorAffiliation | 3 MRC Medical Bioinformatics Centre, University of Leeds, Leeds, LS2 9NL, UK 1 Leeds Institute of Biomedical & Clinical Sciences, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom 2 Leeds Institute of Cancer Studies and Pathology, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom |
AuthorAffiliation_xml | – name: 1 Leeds Institute of Biomedical & Clinical Sciences, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom – name: 2 Leeds Institute of Cancer Studies and Pathology, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom – name: 3 MRC Medical Bioinformatics Centre, University of Leeds, Leeds, LS2 9NL, UK |
Author_xml | – sequence: 1 givenname: Milene surname: Volpato fullname: Volpato, Milene organization: Leeds Institute of Biomedical & Clinical Sciences, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom – sequence: 2 givenname: Sarah L surname: Perry fullname: Perry, Sarah L organization: Leeds Institute of Biomedical & Clinical Sciences, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom – sequence: 3 givenname: Gemma surname: Marston fullname: Marston, Gemma organization: Leeds Institute of Biomedical & Clinical Sciences, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom – sequence: 4 givenname: Nicola surname: Ingram fullname: Ingram, Nicola organization: Leeds Institute of Biomedical & Clinical Sciences, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom – sequence: 5 givenname: Andrew J surname: Cockbain fullname: Cockbain, Andrew J organization: Leeds Institute of Biomedical & Clinical Sciences, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom – sequence: 6 givenname: Heather surname: Burghel fullname: Burghel, Heather organization: Leeds Institute of Biomedical & Clinical Sciences, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom – sequence: 7 givenname: Jake surname: Mann fullname: Mann, Jake organization: Leeds Institute of Biomedical & Clinical Sciences, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom – sequence: 8 givenname: David surname: Lowes fullname: Lowes, David organization: Leeds Institute of Biomedical & Clinical Sciences, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom – sequence: 9 givenname: Erica surname: Wilson fullname: Wilson, Erica organization: Leeds Institute of Cancer Studies and Pathology, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom – sequence: 10 givenname: Alastair surname: Droop fullname: Droop, Alastair organization: MRC Medical Bioinformatics Centre, University of Leeds, Leeds, LS2 9NL, UK – sequence: 11 givenname: Juliette surname: Randerson-Moor fullname: Randerson-Moor, Juliette organization: Leeds Institute of Cancer Studies and Pathology, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom – sequence: 12 givenname: P Louise surname: Coletta fullname: Coletta, P Louise organization: Leeds Institute of Biomedical & Clinical Sciences, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom – sequence: 13 givenname: Mark A surname: Hull fullname: Hull, Mark A organization: Leeds Institute of Biomedical & Clinical Sciences, Wellcome Trust Brenner Building, St James's University Hospital, Leeds LS9 7TF, United Kingdom |
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Cites_doi | 10.1111/j.1476-5381.2012.01882.x 10.1016/j.bbalip.2014.08.010 10.1158/1078-0432.CCR-08-2491 10.1158/1078-0432.CCR-09-1631 10.1111/sji.12240 10.1152/ajpgi.00252.2012 10.1158/1055-9965.EPI-14-0699-T 10.1002/hep.26094 10.1016/j.surg.2011.12.018 10.1016/0022-1759(83)90303-4 10.2147/CEG.S43457 10.1007/s10585-007-9060-3 10.1593/neo.10388 10.1158/1078-0432.CCR-15-0204 10.1158/0008-5472.CAN-09-1451 10.1016/j.bpg.2011.08.001 10.1136/gutjnl-2013-306445 10.1016/j.rmed.2007.02.021 10.1074/jbc.M112.365999 10.1053/j.gastro.2009.11.005 10.1038/nature13931 10.1084/jem.20141836 10.1186/gb-2004-5-10-r80 10.1136/gut.2004.059824 10.1136/gut.2009.200642 10.1038/nature10138 10.2337/db12-1042 10.1136/gut.2010.233718 10.3945/jn.111.142240 10.1093/biostatistics/4.2.249 |
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Keywords | colorectal cancer eicosapentaenoic acid and biomarker prognosis molecular pharmacology |
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References | Calder (6) 2015; 1851 Mapp (15) 2007; 101 Hull (2) 2012; 61 Murphy (26) 2012; 303 Kern (10) 2013; 62 Miyazaki (11) 2009; 34 Hull (12) 2010; 12 Speed (32) 2003; 4 Algul (7) 2014; 7 Cheng (25) 2012; 287 Darzi (22) 2007; 24 Matsushima (21) 2000; 6 Ran (20) 2009; 15 Newton-Bishop (31) 2009; 15 Danish Childhood Diabetes (19) 2014; 80 Hull (14) 2012; 166 Pollard (8) 2011; 475 Hull (3) 2010; 59 35 Pollard (27) 2015; 212 Hull (5) 2011; 25 Mukaida (9) 2009; 69 Mosmann (30) 1983; 65 McLeod (1) 2012; 151 Shiels (18) 2014; 23 Hull (4) 2014; 63 De Palma (29) 2014; 515 Kulig (23) 2015; 125 Muschel (16) 2013; 57 Leisch (34) 2004; 5 Coffey (13) 2010; 138 Sakamoto (24) 2006; 55 Gardner (17) 2011; 141 Dabrosin (28) 2015; 21 R Development Core Team (33) 2011 |
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SubjectTerms | Animals Antineoplastic Agents - therapeutic use Biomarkers, Tumor - blood Chemokine CCL2 - blood Colorectal Neoplasms - drug therapy Colorectal Neoplasms - mortality Colorectal Neoplasms - pathology Disease-Free Survival Eicosapentaenoic Acid - therapeutic use Female Humans Kaplan-Meier Estimate Liver Neoplasms - drug therapy Liver Neoplasms - secondary Liver Neoplasms - surgery Male Mice Mice, Inbred C57BL Research Paper Treatment Outcome |
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Title | Changes in plasma chemokine C-C motif ligand 2 levels during treatment with eicosapentaenoic acid predict outcome in patients undergoing surgery for colorectal cancer liver metastasis |
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