TY - JOUR
T1 - Prognostic significance of CXCL12 expression in patients with colorectal carcinoma
AU - Akishima-Fukasawa, Yuri
AU - Nakanishi, Yukihiro
AU - Ino, Yoshinori
AU - Moriya, Yoshihiro
AU - Kanai, Yae
AU - Hirohashi, Setsuo
PY - 2009/8
Y1 - 2009/8
N2 - The present study investigated the protein expression level of CXCL12 in colorectal cancer and aimed to elucidate its association with prognosis. CXCL12 positivity in 50% or more of tumor cells was defined as high expression and that in less than 50% of the tumor cells as low expression. CXCL12+ tumor budding at the invasive front was divided into 2 grades: high with 10 or more budding foci per x200 field of view and low grade with fewer than 10 budding foci. Patients with high expression (72.7%) and high grade CXCL12+ tumor budding (43.0%) had significantly shorter survival than patients with low expression (P = .014) and low grade (P = .003), respectively. Patients with a combination of high expression and high grade had the worst outcome (P < .001). Our study demonstrated that CXCL12 expression in colorectal cancer cells and at sites of budding were significant prognostic factors. Furthermore, together with lymph node metastasis, a combination of both expression patterns was a more powerful independent prognostic factor.
AB - The present study investigated the protein expression level of CXCL12 in colorectal cancer and aimed to elucidate its association with prognosis. CXCL12 positivity in 50% or more of tumor cells was defined as high expression and that in less than 50% of the tumor cells as low expression. CXCL12+ tumor budding at the invasive front was divided into 2 grades: high with 10 or more budding foci per x200 field of view and low grade with fewer than 10 budding foci. Patients with high expression (72.7%) and high grade CXCL12+ tumor budding (43.0%) had significantly shorter survival than patients with low expression (P = .014) and low grade (P = .003), respectively. Patients with a combination of high expression and high grade had the worst outcome (P < .001). Our study demonstrated that CXCL12 expression in colorectal cancer cells and at sites of budding were significant prognostic factors. Furthermore, together with lymph node metastasis, a combination of both expression patterns was a more powerful independent prognostic factor.
KW - CXCL12
KW - Colorectal carcinoma
KW - Immunohistochemistry
KW - Invasive front
KW - Prognosis
UR - http://www.scopus.com/inward/record.url?scp=68549096319&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=68549096319&partnerID=8YFLogxK
U2 - 10.1309/AJCPK35VZJEWCUTL
DO - 10.1309/AJCPK35VZJEWCUTL
M3 - Article
C2 - 19605814
AN - SCOPUS:68549096319
SN - 0002-9173
VL - 132
SP - 202
EP - 210
JO - American Journal of Clinical Pathology
JF - American Journal of Clinical Pathology
IS - 2
ER -