TY - JOUR
T1 - Cytolytic activity score as a biomarker for antitumor immunity and clinical outcome in patients with gastric cancer
AU - Hu, Qingjiang
AU - Nonaka, Kentaro
AU - wakiyama, hiroaki
AU - Miyashita, Yu
AU - Fujimoto, Yoshiaki
AU - Jogo, Tomoko
AU - Hokonohara, Kentaro
AU - Nakanishi, Ryota
AU - Hisamatsu, Yuichi
AU - Andou, Kouji
AU - Kimura, Yasue
AU - Masuda, Takaaki
AU - Oki, Eiji
AU - Mimori, Koshi
AU - Oda, Yoshinao
AU - Mori, Masaki
N1 - Funding Information:
The authors thank K Oda, K Kasagi, S Sakuma, Y Kubota, A Nakamura, and S Tsurumaru for their technical assistance. This work was supported in part by the following grants and foundations: Japan Society for the Promotion of Science (JSPS) Grant‐in‐Aid for Science Research (grant numbers JP19K16718), Hirose Foundation.
Publisher Copyright:
© 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.
PY - 2021/5
Y1 - 2021/5
N2 - Background: A simple measure of immune cytolytic activity (CYT) base on mRNA expression levels of two genes, GZMA and PRF1, was recently reported. Here, we aimed to evaluate the CYT score's potential as a measure of antitumor immunity and predictor of clinical outcome in gastric cancer (GC) patients. Materials and Methods: We evaluated the correlations between tumor-infiltrating immune cells and the CYT score in 238 GC samples from The Cancer Genome Atlas (TCGA). Next, we investigated CYT score associations with molecular subtypes, somatic mutation load, and immune checkpoint molecules in GC samples from TCGA and Asian Cancer Research Group (ACRG). Moreover, we evaluated the clinical significance of the CYT score calculated by reverse transcription (RT)-quantitative PCR (qPCR) data in 123 GC samples and the association of the CYT score with the response to anti-PD-1 therapy in 7 GC samples from Kyushu University Hospital. Results: The CYT score positively correlated with the proportions of tumor-infiltrating CD8+ T cells and macrophages and negatively correlated with the proportion of regulatory T cells in GC tissues. A high CYT score was associated with common immune checkpoint molecules, a high mutation, the Epstein–Barr virus subtype, and the microsatellite instability subtype in GC. Moreover, a low CYT score was a poor prognosis factor in patients with GC. Finally, the CYT score was higher in a responder to anti-PD-1 therapy compared to nonresponders. Conclusion: The CYT score reflects antitumor immunity and predicts clinical outcome in GC patients.
AB - Background: A simple measure of immune cytolytic activity (CYT) base on mRNA expression levels of two genes, GZMA and PRF1, was recently reported. Here, we aimed to evaluate the CYT score's potential as a measure of antitumor immunity and predictor of clinical outcome in gastric cancer (GC) patients. Materials and Methods: We evaluated the correlations between tumor-infiltrating immune cells and the CYT score in 238 GC samples from The Cancer Genome Atlas (TCGA). Next, we investigated CYT score associations with molecular subtypes, somatic mutation load, and immune checkpoint molecules in GC samples from TCGA and Asian Cancer Research Group (ACRG). Moreover, we evaluated the clinical significance of the CYT score calculated by reverse transcription (RT)-quantitative PCR (qPCR) data in 123 GC samples and the association of the CYT score with the response to anti-PD-1 therapy in 7 GC samples from Kyushu University Hospital. Results: The CYT score positively correlated with the proportions of tumor-infiltrating CD8+ T cells and macrophages and negatively correlated with the proportion of regulatory T cells in GC tissues. A high CYT score was associated with common immune checkpoint molecules, a high mutation, the Epstein–Barr virus subtype, and the microsatellite instability subtype in GC. Moreover, a low CYT score was a poor prognosis factor in patients with GC. Finally, the CYT score was higher in a responder to anti-PD-1 therapy compared to nonresponders. Conclusion: The CYT score reflects antitumor immunity and predicts clinical outcome in GC patients.
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U2 - 10.1002/cam4.3828
DO - 10.1002/cam4.3828
M3 - Article
C2 - 33769705
AN - SCOPUS:85103169995
SN - 2045-7634
VL - 10
SP - 3129
EP - 3138
JO - Cancer Medicine
JF - Cancer Medicine
IS - 9
ER -