TY - JOUR
T1 - PD-L1 expression in papillary renal cell carcinoma
AU - Motoshima, Takanobu
AU - Komohara, Yoshihiro
AU - Ma, Chaoya
AU - Dewi, Arni Kusuma
AU - Noguchi, Hirotsugu
AU - Yamada, Sohsuke
AU - Nakayama, Toshiyuki
AU - Kitada, Shohei
AU - Kawano, Yoshiaki
AU - Takahashi, Wataru
AU - Sugimoto, Masaaki
AU - Takeya, Motohiro
AU - Fujimoto, Naohiro
AU - Oda, Yoshinao
AU - Eto, Masatoshi
N1 - Publisher Copyright:
© 2017 The Author(s).
PY - 2017/1/13
Y1 - 2017/1/13
N2 - Background: The immune escape or tolerance of cancer cells is considered to be closely involved in cancer progression. Programmed death-1 (PD-1) is an inhibitory receptor expressed on activating T cells, and several types of cancer cells were found to express PD-1 ligand 1 (PD-L1) and ligand 2 (PD-L2). Methods: In the present study, we investigated PD-L1/2 expression in papillary renal cell carcinoma (pRCC). Result: We found PD-L1 expression in 29 of 102 cases, but no PD-L2 expression was seen. PD-L1 expression was not significantly correlated with any clinicopathological factor, including progression-free survival and overall survival. The frequency of PD-L1-positive cases was higher in type 2 (36%) than in type 1 (22%) pRCC; however, there was no significant difference in the percentages of score 0 cases (p value = 0.084 in Chi-square test). The frequency of high PD-L1 expression cases was higher in type 2 (23%) than in type 1 (11%), and the frequency of high PD-L1 expression cases was higher in grade 3/4 (21%) than in grade 1/2 (13%). However, no significant association was found between PD-L1 expression and all clinicopathological factors in pRCC. Conclusion: High expression of PD-L1 in cancer cells was potentially associated to highly histological grade of malignancy in pRCC. The evaluation of the PD-L1 protein might still be useful for predicting the efficacy of anti-cancer immunotherapy using immuno-checkpoint inhibitors, however, not be useful for predicting the clinical prognosis.
AB - Background: The immune escape or tolerance of cancer cells is considered to be closely involved in cancer progression. Programmed death-1 (PD-1) is an inhibitory receptor expressed on activating T cells, and several types of cancer cells were found to express PD-1 ligand 1 (PD-L1) and ligand 2 (PD-L2). Methods: In the present study, we investigated PD-L1/2 expression in papillary renal cell carcinoma (pRCC). Result: We found PD-L1 expression in 29 of 102 cases, but no PD-L2 expression was seen. PD-L1 expression was not significantly correlated with any clinicopathological factor, including progression-free survival and overall survival. The frequency of PD-L1-positive cases was higher in type 2 (36%) than in type 1 (22%) pRCC; however, there was no significant difference in the percentages of score 0 cases (p value = 0.084 in Chi-square test). The frequency of high PD-L1 expression cases was higher in type 2 (23%) than in type 1 (11%), and the frequency of high PD-L1 expression cases was higher in grade 3/4 (21%) than in grade 1/2 (13%). However, no significant association was found between PD-L1 expression and all clinicopathological factors in pRCC. Conclusion: High expression of PD-L1 in cancer cells was potentially associated to highly histological grade of malignancy in pRCC. The evaluation of the PD-L1 protein might still be useful for predicting the efficacy of anti-cancer immunotherapy using immuno-checkpoint inhibitors, however, not be useful for predicting the clinical prognosis.
UR - http://www.scopus.com/inward/record.url?scp=85010399626&partnerID=8YFLogxK
U2 - 10.1186/s12894-016-0195-x
DO - 10.1186/s12894-016-0195-x
M3 - Article
C2 - 28086852
AN - SCOPUS:85010399626
SN - 1471-2490
VL - 17
SP - 1
EP - 6
JO - BMC Urology
JF - BMC Urology
IS - 1
M1 - 8
ER -