TY - JOUR
T1 - A complex pattern of chemokine receptor expression is seen in osteosarcoma
AU - von Luettichau, Irene
AU - Segerer, Stephan
AU - Wechselberger, Alexandra
AU - Notohamiprodjo, Mike
AU - Nathrath, Michaela
AU - Kremer, Markus
AU - Henger, Anna
AU - Djafarzadeh, Roghieh
AU - Burdach, Stefan
AU - Huss, Ralf
AU - Nelson, Peter J.
N1 - Funding Information:
This work was supported by the Madleine Schickedanz KinderKrebsstiftung and STMWK Bayern Kapitel 1528 Bu IX/8-3a71a10-9b/32439 to IvL. EU F6 INNOCHEM, DFG 468/2-2 and TR-SFB 36 to PJN. We thank Wiebke Buck, Dan Draganovic and Sabine Moosmann for technical support. The authors would also like to thank Millenium Inc. for providing antibody reagents to CCR10 and CCR4, Matthias Mack and Elisabeth Kremmer for providing the CCR5 and CXCR5 antibodies respectively. We thank the COSS/ EURAMOS database for kindly providing the clinical follow up of some of the patients. We also thank Tibor Schuster, Institute for Medical Statistics and Epidemiology, for consulting on statistical analysis.
PY - 2008/1/24
Y1 - 2008/1/24
N2 - Background: Osteosarcoma is the most frequent bone tumor in childhood and adolescence. Patients with primary metastatic disease have a poor prognosis. It is therefore important to better characterize the biology of this tumor to define new prognostic markers or therapeutic targets for tailored therapy. Chemokines and their receptors have been shown to be involved in the development and progression of malignant tumors. They are thought to be active participants in the biology of osteosarcoma. The function of specific chemokines and their receptors is strongly associated with the biological context and microenvironment of their expression. In this report we characterized the expression of a series of chemokine receptors in the complex environment that defines osteosarcoma. Methods: The overall level of chemokine receptor mRNA expression was determined using TaqMan RT-PCR of microdissected archival patient biopsy samples. Expression was then verified at the protein level by immunohistochemistry using a series of receptor specific antibody reagents to elucidate the cellular association of expression. Results: Expression at the RNA level was found for most of the tested receptors. CCR1 expression was found on infiltrating mononuclear and polynuclear giant cells in the tumor. Cells associated with the lining of intratumoral vessels were shown to express CCR4. Infiltrating mononuclear cells and tumor cells both showed expression of the receptor CCR5, while CCR7 was predominantly expressed by the mononuclear infiltrate. CCR10 was only very rarely detected in few scattered infiltrating cells. Conclusion: Our data elucidate for the first time the cellular context of chemokine receptor expression in osteosarcoma. This is an important issue for better understanding potential chemokine/chemokine receptor function in the complex biologic processes that underlie the development and progression of osteosarcoma. Our data support the suggested involvement of chemokines and their receptors in diverse aspects of the biology of osteosarcoma, but also contradict aspects of previous reports describing the expression of these receptors in this tumor.
AB - Background: Osteosarcoma is the most frequent bone tumor in childhood and adolescence. Patients with primary metastatic disease have a poor prognosis. It is therefore important to better characterize the biology of this tumor to define new prognostic markers or therapeutic targets for tailored therapy. Chemokines and their receptors have been shown to be involved in the development and progression of malignant tumors. They are thought to be active participants in the biology of osteosarcoma. The function of specific chemokines and their receptors is strongly associated with the biological context and microenvironment of their expression. In this report we characterized the expression of a series of chemokine receptors in the complex environment that defines osteosarcoma. Methods: The overall level of chemokine receptor mRNA expression was determined using TaqMan RT-PCR of microdissected archival patient biopsy samples. Expression was then verified at the protein level by immunohistochemistry using a series of receptor specific antibody reagents to elucidate the cellular association of expression. Results: Expression at the RNA level was found for most of the tested receptors. CCR1 expression was found on infiltrating mononuclear and polynuclear giant cells in the tumor. Cells associated with the lining of intratumoral vessels were shown to express CCR4. Infiltrating mononuclear cells and tumor cells both showed expression of the receptor CCR5, while CCR7 was predominantly expressed by the mononuclear infiltrate. CCR10 was only very rarely detected in few scattered infiltrating cells. Conclusion: Our data elucidate for the first time the cellular context of chemokine receptor expression in osteosarcoma. This is an important issue for better understanding potential chemokine/chemokine receptor function in the complex biologic processes that underlie the development and progression of osteosarcoma. Our data support the suggested involvement of chemokines and their receptors in diverse aspects of the biology of osteosarcoma, but also contradict aspects of previous reports describing the expression of these receptors in this tumor.
UR - http://www.scopus.com/inward/record.url?scp=40149105104&partnerID=8YFLogxK
U2 - 10.1186/1471-2407-8-23
DO - 10.1186/1471-2407-8-23
M3 - Article
C2 - 18215331
AN - SCOPUS:40149105104
SN - 1471-2407
VL - 8
JO - BMC Cancer
JF - BMC Cancer
M1 - 23
ER -