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HOME > J Pathol Transl Med > Volume 44(2); 2010 > Article
Original Article Lyn Expression in Osteoblastic Osteosarcoma Tissues and Its Correlation with Clinicopathologic Factors.
Min Sun Jin, Shin Kwang Khang, Min Suk Kim, Hee Seung Choi, Jung Eun Lee, Kil Ho Kim, Dae Geun Jeon, Jae Soo Koh
Journal of Pathology and Translational Medicine 2010;44(2):125-131
DOI: https://doi.org/10.4132/KoreanJPathol.2010.44.2.125
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1Department of Pathology, Korea Cancer Center Hospital, Seoul, Korea. jskoh@kcch.re.kr
2Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
3Laboratory and Experimental Pathology, Korea Institute of Radiological and Medical Sciences, Seoul, Korea.
4Department of Orthopedic Surgery, Korea Cancer Center Hospital, Seoul, Korea.

BACKGROUND
The Src family kinases (SFKs) are involved in multiple aspects of tumorigenesis, such as, proliferation, migration, and angiogenesis, and are involved in the generation and progression of many types of tumors. Furthermore, dasatinib, a general SFKs inhibitor was recently approved for use in chronic myeloid leukemia. This study was performed to evaluate the expression of Lyn, a member of the SFKs, in osteosarcoma tissues.
METHODS
One hundred and sixteen patients with osteoblastic osteosarcoma were selected for Lyn expression analysis. The correlation between Lyn expression in tumor sections and patients' clinicopathologic characteristics and the prognostic significance of Lyn expression were evaluated.
RESULTS
Lyn was found to be expressed in 52 of the 116 patients (44.8%), and Lyn positive tumor was found to be significantly associated with a lytic tumor pattern on plain radiographs (p = 0.04). Furthermore, those positive for Lyn showed longer metastasis free survival (5-year metastasis free survival, 65.2% for Lyn positive and 46.8% for Lyn negative; p = 0.06), though this was only marginally significant.
CONCLUSIONS
Lyn was found to be overexpressed in osteosarcoma tissues, and this overexpression was found to be correlated with osteolysis.


JPTM : Journal of Pathology and Translational Medicine