KMID : 1130320080510010073
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Korean Journal of Pediatrics 2008 Volume.51 No. 1 p.73 ~ p.77
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Clinical significance of loss of p16 protein by immunohistochemical staining in acute lymphoblastic leukemia
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Jin Hye-Young
Yoon Yoo-Sook Kang Joon-Won Jo Deog-Yeon Kwon Kye-Chul Park Kyung-Duk Kang Kyoung-In Kim Sun-Young
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Abstract
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Purpose: p16 gene, mapped to the 9p21 chromosomal region, has emerged as a candidate tumor suppressor
gene in human neoplasm. It is an inhibitor of cyclin-dependent kinase and inhibits Rb phosphorylation. In a variety of tumors including childhood acute lymphoblastic leukemia (ALL), deletion and/or mutation of the p16 gene has been found. Despite their high frequency, the prognostic importance of p16 alterations is still controversial in ALL and has been reported to be either unfavorable or similar to that of other patients. We studied the correlation between loss of p16 protein confirmed by immunohistochemical staining and clinical outcomes of patients diagnosed as ALL.
Methods: We performed an immunohistochemical staining for p16 protein in 74 cases of bone marrow biopsy slide initially diagnosed as ALL between January 1998 and December 2006. We reviewed the clinical manifestations, laboratory findings, treatment outcomes retrospectively.
Results: Of 74 slides, 12 were negative for p16 protein. Seven were males and 5 were females with a median age at diagnosis was 5.8 (1.3-18.8) years. Initial WBC were 17,225 (500-403,300)/¥ìL. By immunologic surface marker analysis, 7 patients were early pre-B CALLA (£«) and 5 patients were T-cell ALL. Two patients of intermediate risk group had relapsed and died. Three patients had family history of breast cancer. Four patients died and overall survival rates were 53.5¡¾18.7%.
Conclusions: Loss of p16 protein is supposed to be an independent risk factor of childhood ALL associated with poor outcomes. In clinical setting, the clinician must take into account p16 status, not only at the genomic but also at the protein level. Further clinical experience on thoroughly investigated cases will help a better understanding between p16 status and clinical outcomes. (Korean J Pediatr 2008;51:73-77)
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KEYWORD
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Leukemia, Lymphocytic, Acute, p16
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