Startseite Hematopoietic cytokines in the sera of patients with pancreatic cancer
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Hematopoietic cytokines in the sera of patients with pancreatic cancer

  • Barbara Mroczko , Maciej Szmitkowski , Urszula Wereszczyńska-Siemiątkowska und Grażyna Jurkowska
Veröffentlicht/Copyright: 1. Juni 2005
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Abstract

Hematopoietic cytokines (HCs) can affect the growth and spread of cancer. Therefore, in the present study, we investigated in pancreatic cancer patients the serum levels of selected HCs, such as stem cell factor (SCF), interleukin 3 (IL-3), granulocyte-macrophage-colony stimulating factor (GM-CSF), granulocyte-colony stimulating factor (G-CSF) and macrophage-colony stimulating factor (M-CSF) in relation to a control group and to a group of patients with chronic pancreatitis. Classical tumor markers such as carcinoembryonic antigen (CEA) and carbohydrate antigen 19-9 (CA 19-9) were also tested. We compared the serum level of cytokines with the tumor stage. The diagnostic sensitivity, specificity, positive and negative predictive values and receiver-operating characteristics (ROC) curve for cytokines and classical tumor markers were defined. The cytokines were measured in 48 patients with pancreatic cancer, in 23 patients with chronic pancreatitis and in 40 healthy subjects. HCs were determined using ELISA. CEA and CA 19-9 were measured by microparticle enzyme immunoassay. There were significant differences in the levels of circulating SCF, IL-3, GM-CSF, M-CSF, CEA and CA 19-9 in the pancreatic cancer patients compared to the control group. The serum levels of M-CSF and tumor markers were significantly higher in pancreatic cancer patients compared to the pancreatitis group. The levels of SCF, M-CSF and tumor markers were higher in patients with a more advanced tumor stage. The M-CSF serum levels in the pancreatitis group correlated positively with the tumor markers tested – CEA and CA 19-9. The diagnostic sensitivity of SCF and specificity of M-CSF and tumor markers were the highest. The SCF and M-CSF areas under the ROC curve were greater than the areas for other cytokines. These results suggest the potential usefulness of HCs in pancreatic cancer detection; however, further investigations of early-stage pancreatic cancer patients and confirmation by a prospective study are necessary.


Corresponding author: M. Szmitkowski MD, PhD, Department of Biochemical Diagnostics, Medical Academy, M. Skłodowska-Curie 24A, 15-276 Białystok, Poland Phone: +48-85-7468587, Fax: +48-85-7468585,

References

1 Tobita K, Kijima H, Dowaki S, Kashiwagi H, Ohtani Y, Oida Y, et al. Epidermal growth factor receptor expression in human pancreatic cancer: significance for liver metastasis. Int J Mol Med 2003; 11: 305–9. 10.3892/ijmm.11.3.305Suche in Google Scholar

2 Bardeesy N, DePinho RA. Pancreatic cancer biology and genetic. Cancer 2002; 2: 897–909. Suche in Google Scholar

3 Uematsu T, Tsuchie K, Ukai K, Kimoto E, Funakawa T, Mizuno R. Granulocyte-colony stimulating factor produced by pancreatic carcinoma. Int J Pancr 1996; 9: 135–9. 10.1007/BF02805227Suche in Google Scholar

4 Dunlop RJ, Campbell CW. Cytokines and advanced cancer. J Pain Sympt Manage 2000; 20: 214–32. 10.1016/S0885-3924(00)00199-8Suche in Google Scholar

5 Esposito I, Kleeff J, Bischoff SC, Fischer L, Collecchi P, Iorio M, et al. The stem cell factor-c-kit system and mast cells in human pancreatic cancer. Lab Invest 2002; 82: 1481–92. 10.1097/01.LAB.0000036875.21209.F9Suche in Google Scholar PubMed

6 McDermott RS, Deneux L, Mosseri V, Vedrenne J, Clough K, Fourquet A, et al. Circulating macrophage colony stimulating factor as a marker of tumor progression. Eur Cytokine Netw 2002; 13: 121–7. Suche in Google Scholar

7 Pei XH, Nakanishi Y, Takayama K, Bai F, Hara N. Granulocyte, granulocyte-macrophage, and macrophage colony-stimulating factors can stimulate the invasive capacity of human lung cancer cells. Br J Cancer 1999; 79: 40–6. 10.1038/sj.bjc.6690009Suche in Google Scholar PubMed PubMed Central

8 Mroczko B, Szmitkowski M, Okulczyk B, Piotrowski Z. Granulocyte-macrophage-colony stimulating factor in patients with colorectal cancer. Folia Hist Cytobiol 2001; 39(Suppl 2): 110–1. 10.1515/CCLM.2001.059Suche in Google Scholar PubMed

9 Mroczko B, Szmitkowski M, Okulczyk B. Granulocyte-colony stimulating factor (G-CSF) and macrophage-colony stimulating factor (M-CSF) in colorectal cancer patients. Clin Chem Lab Med 2002; 40: 351–5. 10.1515/CCLM.2002.056Suche in Google Scholar PubMed

10 Mroczko B, Szmitkowski M, Okulczyk B. Hematopoietic growth factors in colorectal cancer patients. Clin Chem Lab Med 2003; 41: 646–51. 10.1515/CCLM.2003.098Suche in Google Scholar PubMed

11 Mroczko B, Szmitkowski M, Wereszczynska-Siemiatkowska U, Jurkowska G. Stem cell factor and macrophage-colony stimulating factor in patients with pan- creatic cancer. Clin Chem Lab Med 2004; 42: 256–60. 10.1515/CCLM.2004.047Suche in Google Scholar PubMed

12 Rosch T. The new TNM classification in gastroenterology (1997). Endoscopy 1998; 30: 643–9. Suche in Google Scholar

13 Kairisto V, Virtanen A, Uusipaikka E, Voipio-Pulkki LM, Nanto V, Peltola O, et al. Method for determining reference changes from patients serial data: example of cardiac enzymes. Clin Chem 1993; 39: 2298–304. 10.1093/clinchem/39.11.2298Suche in Google Scholar

14 Parker SL, Tong T, Bolden S, Wingo PA. Cancer statistics. CA Cancer J Clin 1997; 47: 5–27. 10.3322/canjclin.47.1.5Suche in Google Scholar

15 Nemunaitis J. A comparative review of colony-stimula ting factors. Drugs 1997; 54: 709–29. 10.2165/00003495-199754050-00004Suche in Google Scholar

16 Trutmann M, Terracciano L, Noppen C, Kloth J, Kaspar M, Peterli R, et al. GM-CSF gene expression and protein production in human colorectal cell lines and clinical tumor specimens. Int J Cancer 1998; 77: 378–85. 10.1002/(SICI)1097-0215(19980729)77:3<378::AID-IJC12>3.0.CO;2-4Suche in Google Scholar

17 Young MR, Lozano Y, Coogan M. Stimulation of the metastasis properties of Lewis-lung-carcinoma cells by autologous granulocyte macrophage colony-stimula- ting factor. Int J Cancer 1992; 50: 628–34. 10.1002/ijc.2910500424Suche in Google Scholar

18 Chambers SK, Wang Y, Gertz RE, Kacinski BM. Macrophage colony-stimulating factor mediates invasion of ovarian cancer cells through urokinase. Cancer Res 1995; 55: 1578–85. Suche in Google Scholar

19 Mroczko B, Szmitkowski M, Niklinski J. Stem cell factor and granulocyte-macrophage-colony stimulating factor as candidates for tumour markers for non-small-cell lung cancer. Clin Chem Lab Med 1999; 37: 959–62. 10.1515/CCLM.1999.141Suche in Google Scholar

20 Mroczko B, Szmitkowski M, Niklinski J. Granulocyte-colony stimulating factor and macrophage-colony stimulating factor in patients with non-small-cell lung cancer. Clin Chem Lab Med 2001; 39: 374–9. 10.1515/CCLM.2001.059Suche in Google Scholar

Received: 2004-7-5
Accepted: 2004-12-14
Published Online: 2005-6-1
Published in Print: 2005-4-1

©2005 by Walter de Gruyter Berlin New York

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