l-Arginine as a factor increasing arginase significance in diagnosis of primary and metastatic colorectal cancer

Clinical Biochemistry

Volumn 42, Issue 4-5, 2009, Pages 353-357

  Graboń, Wojciech ^a   Mielczarek Puta, Magdalena ^a   Chrzanowska, Alicja ^a   Barańczyk Kuźma, Anna ^a  

^a MEDICAL UNIVERSITY OF WARSAW   (Poland)

Author keywords

Arginase; Colorectal cancer; Colorectal cancer liver metastases; l Arginine

Indexed keywords

ARGINASE; ARGININE;

ADULT; AGED; ARTICLE; CANCER PATIENT; COLORECTAL CANCER; CONTROLLED STUDY; DIAGNOSTIC VALUE; ENZYME ACTIVITY; FEMALE; FOLLOW UP; HUMAN; LIVER METASTASIS; MAJOR CLINICAL STUDY; MALE; POSTOPERATIVE PERIOD; PREOPERATIVE EVALUATION; PRIMARY TUMOR; PRIORITY JOURNAL; SENSITIVITY AND SPECIFICITY; BLOOD; CASE CONTROL STUDY; COLORECTAL NEOPLASMS; ENZYMOLOGY; LIVER NEOPLASMS; MIDDLE AGED; PREOPERATIVE CARE; SECONDARY;

AGED; ARGINASE; ARGININE; CASE-CONTROL STUDIES; COLORECTAL NEOPLASMS; FEMALE; HUMANS; LIVER NEOPLASMS; MALE; MIDDLE AGED; PREOPERATIVE CARE; SENSITIVITY AND SPECIFICITY;

EID: 60949083854     PISSN: 00099120     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.clinbiochem.2008.11.018     Document Type: Article

References (29)

1. Boyle P., and Ferlay J. Cancer incidence and mortality in Europe, 2004. Ann. Oncol. 16 (2005) 481-488
2. Ishizuka D., Shirai Y., Sakai Y., and Hatakeyama K. Colorectal carcinoma liver metastases: clinical significance of preoperative measurement of serum carcinoembryonic antigen and carbohydrate antigen 19-9 levels. Int. J. Colorectal Dis. 16 (2001) 32-37
3. Reiter W., Stieber P., Reuter C., Nagel D., Lau-Werner U., and Lamerz R. Multivariate analysis of the prognostic value of CEA and CA 19-9 serum levels in colorectal cancer. Anticancer Res. 20 (2000) 5195-5198
4. Wu G., and Morris Jr. S.M. Arginine metabolism; nitric oxide and beyond. Biochem. J. 336 (1998) 1-17
5. Wu G., Meininger C., Knabe D.A., Bazer F.W., and Rhoads J.M. Arginine nutrition in development, health and disease. Curr. Opin. Clin. Nutr. Metab. Care. 3 (2000) 59-66
6. Gokmen S.S., Aygit A.C., Ayhan M.S., Yorulmaz F., and Gulen S. Significance of arginase and ornithine in malignant tumors of the human skin. J. Lab. Clin. Med. 137 (2001) 340-344
7. Singh R., Pervin S., Wu G., and Chaudhuri G. Activation of caspase-3 activity and apoptosis in MDA-MB-468 cells by N(omega)-hydroxy-l-arginine, an inhibitor of arginase, is not solely dependent on reduction in intracellular polyamines. Carcinogenesis 22 (2001) 1863-1869
8. Porembska Z., Za{ogonek}bek J., Graboń W., Rahden-Staroń I., and Barańczyk-Kuźma A. Arginase isoforms in human colorectal cancer. Clin. Chim. Acta 305 (2001) 157-165
9. Mielczarek M., Chrzanowska A., Ścibior D., et al. Arginase as a useful factor for the diagnosis of colorectal cancer liver metastases. Int. J. Biol. Markers 21 (2006) 40-44
10. Porembska Z., Skwarek A., Mielczarek M., and Barańczyk-Kuźma A. Serum arginase activity in postsurgical monitoring of patients with colorectal carcinoma. Cancer 94 (2002) 2930-2934
11. Kashyap S.R., Lara A., Zhang R., Park Y.M., and DeFronzo R.A. Insulin reduces plasma arginase activity in type 2 diabetic patients. Diabetes Care 31 (2008) 134-139
12. Morris C.R., Poljakovic M., Lavrisha L., Machado L., Kuypers F.A., and Morris Jr. S.M. Decreased arginine bioavailability and increased serum arginase activity in asthma. Am. J. Respir. Crit. Care Med. 170 (2004) 148-153
13. Yu Y.M., Ryan C.M., Castillo L., et al. Arginine and ornithine kinetics in severely burned patients: increased rate of arginine disposal. Am. J. Physiol., Endocrinol Metabol. 280 (2001) E509-E517
14. Ścibior D., Ashamiss F., Wierzbicki Z., and Barańczyk-Kuźma A. Arginase activity in blood serum of patients with acute and chronic pancreatitis. Pol. Merk. Lek. 126 (2006) 522-524
15. Morris C.R., Kato G.J., Poljakovic M., et al. Dysregulated arginine metabolism, hemolysis-associated pulmonary hypertension, and mortality in sickle cell disease. JAMA 294 (2005) 81-90
16. Gopalakrishna R., and Nagarajan B. A simplified procedure for the estimation of arginine in plasma and urine using arginase. Clin. Chim. Acta. 106 (1980) 333-337
17. Chinard F.P. Photometric estimation of proline and ornithine. J. Biol. Chem. 199 (1952) 91-95
18. Caso G., McNurlan M.A., McMillan N.D., Eremin O., and Garlick P.J. Tumour cell growth in culture: dependence on arginine. Clin. Sci. (Lond) 107 (2004) 371-379
19. Cendan J.C., Souba W.W., Copeland III E.M., and Lind D.S. Characterization and growth factor stimulation of l-arginine transport in a human colon cancer cell line. Ann. Surg. Oncol. 2 (1995) 257-265
20. Cendan J.C., Souba W.W., Copeland III E., and Lind D.S. Increased l-arginine transport in a nitric oxide-producing metastatic colon cancer cell line. Ann. Surg. Oncol. 3 (1996) 501-508
21. Huang S., Trujillo J.M., and Chakrabarty S. Proliferation of human colon cancer cells: role of epidermal growth factor and transforming growth factor alpha. Int. J. Cancer 52 (1992) 978-986
22. Vissers Y.L., Dejong C.H., Luiking Y.C., Fearon K.C., von Meyenfeldt M.F., and Deutz N.E. Plasma arginine concentrations are reduced in cancer patients: evidence for arginine deficiency?. Am. J. Clin. Nutr. 81 (2005) 1126-1142
23. Glass R.E., Goode A.W., Houghton B.J., and Rowell L.W. Plasma arginine in cancer of the gastrointestinal tract: effect of surgical treatment. Gut 27 (1986) 844-848
24. Ma Q., Wang Y., Gao X., Ma Z., and Song Z. L-arginine reduces cell proliferation and ornithine decarboxylase activity in patients with colorectal adenoma and adenocarcinoma. Clin. Cancer Res. 13 (2007) 7407-7412
25. Kojima M., Morisaki T., Tsukahara Y., et al. Nitric oxide synthase expression and nitric oxide production in human colon carcinoma tissue. J. Surg. Oncol. 70 (1999) 222-229
26. Grasemann H., Schwiertz R., Grasemann C., Vester U., Racké K., and Ratjen F. Decreased systemic bioavailability of L-arginine in patients with cystic fibrosis. Respir. Res. 7 (2006) 87
27. Sandstrom P., Trulsson L., Gasslander T., Sundqvist T., von Dobeln U., and Svanvik J. Serum amino acid profile in patients with acute pancreatitis. Amino Acids 35 (2008) 225-231
28. Ochoa J.B., Bernard A.C., Mistry S.K., et al. Trauma increases extrahepatic arginase activity. Surgery 127 (2000) 419-426
29. Tsuei B.J., Bernard A.C., Shane M.D., et al. Surgery induces human mononuclear cell arginase I expression. J. Trauma. 51 (2001) 497-502