TY - JOUR
T1 - Aberrant fatty acid-binding protein-7 gene expression in cutaneous malignant melanoma
AU - Goto, Yasufumi
AU - Koyanagi, Kazuo
AU - Narita, Norihiko
AU - Kawakami, Yutaka
AU - Takata, Minoru
AU - Uchiyama, Aya
AU - Nguyen, Linhda
AU - Nguyen, Tung
AU - Ye, Xing
AU - Morton, Donald L.
AU - Hoon, Dave S.B.
N1 - Funding Information:
We thank Kana Rivera for editorial assistance. This study was supported by National Cancer Institute project II PO CA029605 and CA012582, Weil Family Fund (Los Angeles, CA) and the Leslie and Susan Gonda (Goldschmied) Foundation (Los Angeles, CA).
PY - 2010/1
Y1 - 2010/1
N2 - Fatty acid-binding protein-7 (FABP7) has been shown to be expressed in cutaneous melanoma; however, its role in tumor progression is unclear. Expression of FABP7 was assessed during melanoma progression through assessment of various clinicopathology stages of primary tumor progression and metastasis. FABP7 mRNA was highly expressed in 60 of 87 (69%) primary melanomas, compared with significant (P0.0001) reduction in 13 of 68 (19%) metastatic melanomas. Analysis of 37 paired primary and metastatic melanomas by immunohistochemistry with anti-FABP7 Ab showed 73 and 27% positivity, respectively (P0.001). FABP7 detection of metastatic tissues was inversely correlated with relapse-free (P0.0001) and overall (P0.0001) survival. To examine FABP7 expression loss in advanced melanomas, loss of heterozygosity (LOH) was assessed using microsatellite markers encompassing the FABP7 gene. LOH was identified in 10 of 20 (50%) metastatic melanomas at 6q22.31, compared with 0 of 14 primary melanomas (P0.0017). FABP7 as a surrogate biomarker for circulating tumor cells (CTCs) in the blood was assessed by quantitative real-time (qRT)-PCR from melanoma patients blood (n134). Assessment of patients blood showed that FABP7() CTC decreased with disease progression. FABP7 may function as a tumor progression gene and can be used as a potential diagnostic biomarker of early-stage melanoma systemic spreading in blood.
AB - Fatty acid-binding protein-7 (FABP7) has been shown to be expressed in cutaneous melanoma; however, its role in tumor progression is unclear. Expression of FABP7 was assessed during melanoma progression through assessment of various clinicopathology stages of primary tumor progression and metastasis. FABP7 mRNA was highly expressed in 60 of 87 (69%) primary melanomas, compared with significant (P0.0001) reduction in 13 of 68 (19%) metastatic melanomas. Analysis of 37 paired primary and metastatic melanomas by immunohistochemistry with anti-FABP7 Ab showed 73 and 27% positivity, respectively (P0.001). FABP7 detection of metastatic tissues was inversely correlated with relapse-free (P0.0001) and overall (P0.0001) survival. To examine FABP7 expression loss in advanced melanomas, loss of heterozygosity (LOH) was assessed using microsatellite markers encompassing the FABP7 gene. LOH was identified in 10 of 20 (50%) metastatic melanomas at 6q22.31, compared with 0 of 14 primary melanomas (P0.0017). FABP7 as a surrogate biomarker for circulating tumor cells (CTCs) in the blood was assessed by quantitative real-time (qRT)-PCR from melanoma patients blood (n134). Assessment of patients blood showed that FABP7() CTC decreased with disease progression. FABP7 may function as a tumor progression gene and can be used as a potential diagnostic biomarker of early-stage melanoma systemic spreading in blood.
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U2 - 10.1038/jid.2009.195
DO - 10.1038/jid.2009.195
M3 - Article
C2 - 19587692
AN - SCOPUS:72049127502
SN - 0022-202X
VL - 130
SP - 221
EP - 229
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
IS - 1
ER -