TY - JOUR
T1 - Concordant overexpression of phosphorylated ATF2 and STAT3 in extramammary Paget's disease
AU - Chen, Si Yuan
AU - Takeuchi, Satoshi
AU - Moroi, Yoichi
AU - Hayashida, Sayaka
AU - Kido, Makiko
AU - Tomoeda, Hiroto
AU - Uenotsuchi, Takeshi
AU - Tu, Ya Ting
AU - Furue, Masutaka
AU - Urabe, Kazunori
PY - 2009/4
Y1 - 2009/4
N2 - Background: Activating transcription factor 2 (ATF2) and signal transducer and activator of transcription 3 (STAT3) play important roles in the pathogenesis of various tumors, but ATF2 expression/activation and the relationship with STAT3 activation have not yet been investigated in extramammary Paget's disease (EMPD). Objective: To investigate potential contributions of ATF2 and STAT3 pathways to the pathogenesis of EMPD. Method: Paraffin-embedded 45 EMPD specimens (43 primary EMPD and 2 nodal metastases) were subjected to immunohistochemical staining for ATF2, phosphorylated (p)-ATF2 and p-STAT3. Results: P-ATF2 expression in advanced EMPD, non-invasive EMPD and normal skin (NS) controls were 97.9 ± 1.8%, 82.0 ± 23.4% and 45.8 ± 3.2%, respectively, and p-STAT3 expression in advanced EMPD, non-invasive EMPD and NS were 97.0 ± 2.9%, 83.2 ± 23.3% and 50.1 ± 6.7%, respectively. P-ATF2 and p-STAT3 expressions in EMPD were significantly higher than those in NS, indicating a possible contribution of these pathways to the tumor development. P-ATF2 and p-STAT3 expressions in advanced EMPD were significantly higher than those in non-invasive EMPD, possibly indicating that these pathways might also contribute to the tumor invasion and/or metastasis. We also found an exceptionally high positive correlation between p-ATF2 and p-STAT3 expressions in EMPD. Conclusions: P-ATF2 and p-STAT3 are concordantly overexpressed in EMPD and their expressions may possibly be associated with the tumor stage. Chen S-Y, Takeuchi S, Moroi Y, Hayashida S, Kido M, Tomoeda H, Uenotsuchi T, Tu Y-T, Furue M, Urabe K. Concordant overexpression of phosphorylated ATF2 and STAT3 in extramammary Paget's disease.
AB - Background: Activating transcription factor 2 (ATF2) and signal transducer and activator of transcription 3 (STAT3) play important roles in the pathogenesis of various tumors, but ATF2 expression/activation and the relationship with STAT3 activation have not yet been investigated in extramammary Paget's disease (EMPD). Objective: To investigate potential contributions of ATF2 and STAT3 pathways to the pathogenesis of EMPD. Method: Paraffin-embedded 45 EMPD specimens (43 primary EMPD and 2 nodal metastases) were subjected to immunohistochemical staining for ATF2, phosphorylated (p)-ATF2 and p-STAT3. Results: P-ATF2 expression in advanced EMPD, non-invasive EMPD and normal skin (NS) controls were 97.9 ± 1.8%, 82.0 ± 23.4% and 45.8 ± 3.2%, respectively, and p-STAT3 expression in advanced EMPD, non-invasive EMPD and NS were 97.0 ± 2.9%, 83.2 ± 23.3% and 50.1 ± 6.7%, respectively. P-ATF2 and p-STAT3 expressions in EMPD were significantly higher than those in NS, indicating a possible contribution of these pathways to the tumor development. P-ATF2 and p-STAT3 expressions in advanced EMPD were significantly higher than those in non-invasive EMPD, possibly indicating that these pathways might also contribute to the tumor invasion and/or metastasis. We also found an exceptionally high positive correlation between p-ATF2 and p-STAT3 expressions in EMPD. Conclusions: P-ATF2 and p-STAT3 are concordantly overexpressed in EMPD and their expressions may possibly be associated with the tumor stage. Chen S-Y, Takeuchi S, Moroi Y, Hayashida S, Kido M, Tomoeda H, Uenotsuchi T, Tu Y-T, Furue M, Urabe K. Concordant overexpression of phosphorylated ATF2 and STAT3 in extramammary Paget's disease.
UR - http://www.scopus.com/inward/record.url?scp=61449233249&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=61449233249&partnerID=8YFLogxK
U2 - 10.1111/j.1600-0560.2008.01076.x
DO - 10.1111/j.1600-0560.2008.01076.x
M3 - Article
C2 - 19278424
AN - SCOPUS:61449233249
SN - 0303-6987
VL - 36
SP - 402
EP - 408
JO - Journal of Cutaneous Pathology
JF - Journal of Cutaneous Pathology
IS - 4
ER -