TY - JOUR
T1 - Expression of survivin and of antigen detected by a novel monoclonal antibody, T332, is associated with outcome of diffuse large B-cell lymphoma and its subtypes
AU - Watanuki-Miyauchi, Rumiko
AU - Kojima, Yasushi
AU - Tsurumi, Hisashi
AU - Hara, Takeshi
AU - Goto, Naoe
AU - Kasahara, Seiji
AU - Saio, Masanao
AU - Moriwaki, Hisataka
AU - Takami, Tsuyoshi
PY - 2005/6
Y1 - 2005/6
N2 - Although diffuse large B-cell lymphoma (DLBCL) is the most common type of non-Hodgkin lymphoma, it is both clinically and morphologically heterogenous. The present study investigates the significance of survivin and a novel monoclonal antibody (MAb), T332, immunohistochemically for predicting the prognoses of DLBCL and its subtypes classified as germinal center B-cell-like type (GCB) and non-GCB type (NGCB) based on the expression profiles of CD10, bcl-6, and MUM1. A total of 60 cases of DLBCL (GCB, n = 22; NGCB, n = 38) were examined for the expression of survivin and T332 antigen. Survivin+ DLBCL had a significantly worse prognosis (P =0.01) than survivin- cases, as already reported, while survivin+ GCB or NGCB tended to have poor prognoses (P = 0.06 and 0.07, respectively). However, T332+ DLBCL and NGCB had significantly more unfavorable prognoses than T332 - cases (P = 0.01 and 0.02, respectively) while there was no significant survival difference between the T332+ and T332 - groups of GCB (P = 0.11). Interestingly DLBCL coexpressing survivin and T332 (n = 13) had a significantly worse prognosis (P = 0.009) than the remaining single positive and double negative cases (n = 31). In conclusion, survivin and the novel MAb, T332, might be a good predictor of DLBCL and its subtypes.
AB - Although diffuse large B-cell lymphoma (DLBCL) is the most common type of non-Hodgkin lymphoma, it is both clinically and morphologically heterogenous. The present study investigates the significance of survivin and a novel monoclonal antibody (MAb), T332, immunohistochemically for predicting the prognoses of DLBCL and its subtypes classified as germinal center B-cell-like type (GCB) and non-GCB type (NGCB) based on the expression profiles of CD10, bcl-6, and MUM1. A total of 60 cases of DLBCL (GCB, n = 22; NGCB, n = 38) were examined for the expression of survivin and T332 antigen. Survivin+ DLBCL had a significantly worse prognosis (P =0.01) than survivin- cases, as already reported, while survivin+ GCB or NGCB tended to have poor prognoses (P = 0.06 and 0.07, respectively). However, T332+ DLBCL and NGCB had significantly more unfavorable prognoses than T332 - cases (P = 0.01 and 0.02, respectively) while there was no significant survival difference between the T332+ and T332 - groups of GCB (P = 0.11). Interestingly DLBCL coexpressing survivin and T332 (n = 13) had a significantly worse prognosis (P = 0.009) than the remaining single positive and double negative cases (n = 31). In conclusion, survivin and the novel MAb, T332, might be a good predictor of DLBCL and its subtypes.
UR - https://www.scopus.com/pages/publications/21344458613
UR - https://www.scopus.com/inward/citedby.url?scp=21344458613&partnerID=8YFLogxK
U2 - 10.1111/j.1440-1827.2005.01832.x
DO - 10.1111/j.1440-1827.2005.01832.x
M3 - Article
C2 - 15943789
AN - SCOPUS:21344458613
SN - 1320-5463
VL - 55
SP - 324
EP - 330
JO - Pathology International
JF - Pathology International
IS - 6
ER -