TY - JOUR
T1 - Circulating PD-1 mRNA in Peripheral Blood is a Potential Biomarker for Predicting Survival of Breast Cancer Patients
AU - Noda, Miwa
AU - Masuda, Takaaki
AU - Ito, Shuhei
AU - Tobo, Taro
AU - Kitagawa, Akihiro
AU - Hu, Qingjiang
AU - Shimizu, Dai
AU - Eguchi, Hidetoshi
AU - Etoh, Tsuyoshi
AU - Ohno, Shinji
AU - Inomata, Masafumi
AU - Mimori, Koshi
N1 - Funding Information:
Shinji Ohno has received honoraria from Chugai, Eisai, Taiho, Pfizer, Lilly, Kyowa Hakko Kirin, Novartis and AstraZeneca; grants from Eisai and Chugai, outside the submitted work. The other authors declare no competing interests.
Funding Information:
The authors thank K. Oda, M. Kasagi, S. Sakuma, N. Mishima, T. Kawano, M. Oshiumi, and M. Utou for their technical assistance and Dr. Tyler Lahusen for English proofreading. This work was supported in part by the following grants and foundations: Japan Society for the Promotion of Science Grant-in-Aid for Science Research (Grant Nos. JP16K07177, JP16K10543, JP17K16454, JP17K16521, JP17K10593, and JP17K19608); OITA Cancer Research Foundation; Daiwa Securities Health Foundation; Grant-in-Aid for Scientific Research on Innovative Areas (15H0912); Priority Issue on Post-K computer (hp170227, hp160219); JSPS KAKENHI (15H05707); Japanese Foundation for Multidisciplinary Treatment of Cancer.
Publisher Copyright:
© 2020, Society of Surgical Oncology.
PY - 2020/10/1
Y1 - 2020/10/1
N2 - Background: Programmed cell death 1 (PD-1) inhibitors have shown significant therapeutic promise in various cancers. However, the clinical significance of PD-1 expression remains not fully understood. In this study, we evaluated the clinical and prognostic relevance of PD-1 expression in breast cancer (BC). Methods: First, we analyzed PD-1 mRNA expression in BC tissues and performed a survival analysis using a dataset from The Cancer Genome Atlas. Next, we measured PD-1 mRNA expression in peripheral blood (PB) in BC patients by quantitative reverse-transcription polymerase chain reaction. We performed a survival analysis and evaluated the association between PD-1 mRNA expression in PB and the clinicopathological features of 372 BC patients who underwent curative resection. Flow cytometry (FCM) analysis was performed to identify PD-1-expressing cells in PB. Finally, we determined whether there was a correlation of PD-1 mRNA expression in PB and tumor tissue. Results: PD-1 mRNA expression was significantly higher in tumor tissues compared with normal tissues. Decreased PD-1 mRNA expression in tumor tissue was associated with poor overall survival (OS). PD-1 mRNA expression in PB of BC patients was higher than that of healthy volunteers, and increased PD-1 mRNA expression in PB was associated with poor OS. FCM revealed that PD-1 was mostly expressed on T cells in PB, predominantly in CD4+ T cells. PD-1 mRNA expression in PB was negatively correlated with PD-1 mRNA expression in tumor tissue. Conclusion: High expression of PD-1 mRNA in preoperative PB could serve as an effective biomarker that indicates poor prognosis in BC.
AB - Background: Programmed cell death 1 (PD-1) inhibitors have shown significant therapeutic promise in various cancers. However, the clinical significance of PD-1 expression remains not fully understood. In this study, we evaluated the clinical and prognostic relevance of PD-1 expression in breast cancer (BC). Methods: First, we analyzed PD-1 mRNA expression in BC tissues and performed a survival analysis using a dataset from The Cancer Genome Atlas. Next, we measured PD-1 mRNA expression in peripheral blood (PB) in BC patients by quantitative reverse-transcription polymerase chain reaction. We performed a survival analysis and evaluated the association between PD-1 mRNA expression in PB and the clinicopathological features of 372 BC patients who underwent curative resection. Flow cytometry (FCM) analysis was performed to identify PD-1-expressing cells in PB. Finally, we determined whether there was a correlation of PD-1 mRNA expression in PB and tumor tissue. Results: PD-1 mRNA expression was significantly higher in tumor tissues compared with normal tissues. Decreased PD-1 mRNA expression in tumor tissue was associated with poor overall survival (OS). PD-1 mRNA expression in PB of BC patients was higher than that of healthy volunteers, and increased PD-1 mRNA expression in PB was associated with poor OS. FCM revealed that PD-1 was mostly expressed on T cells in PB, predominantly in CD4+ T cells. PD-1 mRNA expression in PB was negatively correlated with PD-1 mRNA expression in tumor tissue. Conclusion: High expression of PD-1 mRNA in preoperative PB could serve as an effective biomarker that indicates poor prognosis in BC.
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U2 - 10.1245/s10434-020-08375-z
DO - 10.1245/s10434-020-08375-z
M3 - Article
C2 - 32206951
AN - SCOPUS:85082183760
SN - 1068-9265
VL - 27
SP - 4035
EP - 4043
JO - Annals of Surgical Oncology
JF - Annals of Surgical Oncology
IS - 10
ER -