Hepatology 2005, 42 (5) : 1208–36.CrossRefPubMed 17. Shah U, O’Neil B, Allen J, Goldberg RM, Bernard S, Moore D, Venook AP, Morse MM: A Phase II Study of Long-Acting
Octreotide in Patients With Advanced Hepatocellular Carcinoma and CLIP Score of 3 or Higher. Gastrointest Cancer Res 2009, 3 (2) : 45–8.PubMed 18. Barbare JC, Bouché O, Bonnetain F, Dahan L, Lombard-Bohas C, Faroux R, Raoul JL, Cattan S, Lemoine A, Blanc JF, Bronowicki JP, Zarski JP, Cazorla S, Gargot D, Thevenot T, Diaz E, Bastie A, Aparicio T, Bedenne L: Treatment of advanced hepatocellular carcinoma with long-acting octreotide: a phase III multicentre, randomised, double blind placebo-controlled study. Eur J Cancer 2009, 45 (10) : 1788–97.CrossRefPubMed 19. Bläker M, Schmitz M, Gocht A, Burghardt S, Schulz M, Bröring DC, Pace A, Greten H, De Weerth A: Differential expression of somatostatin receptor subtypes AMG510 mw in hepatocellular carcinomas. J Hepatol 2004, 41 (1) : 112–8.CrossRefPubMed 20. Reynaert H, Rombouts K,
Vandermonde A, Urbain D, Kumar U, Bioulac-Sage P, Pinzani M, Rosenbaum J, Geerts A: Expression of somatostatin selleck kinase inhibitor receptors in normal and cirrhotic human liver and in hepatocellular carcinoma. Gut 2004, 53 (8) : 1180–9.CrossRefPubMed 21. Cammà C, Schepis F, Orlando A, Albanese M, Shahied L, Trevisani F, Andreone P, Craxì A, Cottone M: Transarterial chemoembolization for unresectable hepatocellular carcinoma: meta-analysis of randomized controlled trials. Radiology 2002, 224 (1) : 47–54. ReviewCrossRefPubMed 22. Myers RP: Meta-analysis of transarterial embolization in patients with unresectable hepatocellular carcinoma. Radiology 2003, 227 (2) : 611–2. author reply 612–3CrossRefPubMed 23. Plentz RR, Tillmann HL, Kubicka S, Bleck
JS, Gebel M, Manns MP, Rudolph KL: Hepatocellular carcinoma and octreotide: treatment results in prospectively assigned patients with advanced tumor and cirrhosis stage. J A-1210477 solubility dmso Gastroenterol Hepatol 2005, 20 (9) : 1422–8.CrossRefPubMed Competing interests The authors Non-specific serine/threonine protein kinase declare that they have no competing interests. Authors’ contributions JK performed chemoembolization. MPR recruited patients. MSH and CM were equally involved in the design of the study, patient recruitment, management of the patients, statistical analysis and drafted the manuscript. All authors read an approved the final manuscript.”
“Introduction Bone marrow is not only the source of leukemic cells, but is also the primary site of leukemia relapse [1]. For these reasons, the hematopoietic microenvironment (HM) of the bone marrow plays a crucial role in the development and progression of leukemia. Variations in the HM may influence the biological behaviors of leukemia cells; for example, induction of resistance to chemotherapy drugs by hypoxia [2] is now known to involve many components.