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The association between the expression of PD-L1 and CMTM6 in undifferentiated pleomorphic sarcoma

Authors :
Kenichi Kohashi
Yoshihiro Matsumoto
Yasuharu Nakashima
Shinichiro Kawatoko
Hidetaka Yamamoto
Izumi Kinoshita
Kengo Kawaguchi
Toshifumi Fujiwara
Makoto Endo
Nokitaka Setsu
Shin Ishihara
Yu Toda
Daisuke Kiyozawa
Yousuke Susuki
Takeshi Iwasaki
Dai Takamatsu
Taro Mori
Yuichi Yamada
Yoshihiro Ito
Yoshinao Oda
Source :
Journal of cancer research and clinical oncology. 147(7)
Publication Year :
2021

Abstract

Undifferentiated pleomorphic sarcoma (UPS) is a sarcoma with a poor prognosis. A clinical trial, SARC028, revealed that treatment with anti-PD-1 drugs was effective against UPS. Studies have reported that UPS expresses PD-L1, sometimes strongly (≥ 50%). However, the mechanism of PD-L1 expression in UPS has remained unclear. CKLF-like MARVEL transmembrane domain containing 6 (CMTM6) was identified as a novel regulator of PD-L1 expression. The positive relationship between PD-L1 and CMTM6 has been reported in several studies. The aim of this study was thus to examine CMTM6 expression in UPS and evaluate the relationship between PD-L1 and CMTM6 in this disease. Fifty-one primary UPS samples were subjected to CMTM6 and PD-L1 immunostaining. CMTM6 expression was assessed using proportion and intensity scores. CMTM6 gene copy number was also evaluated using a real-time PCR-based copy number assay. We also analyzed the mRNA expression and copy number variation of PD-L1 and CMTM6 in The Cancer Genome Atlas (TCGA) data. TCGA data indicated that the mRNAs encoded by genes located around 3p22 were coexpressed with CMTM6 mRNA in UPS. Both proportion and intensity scores of CMTM6 positively correlated with strong PD-L1 expression (≥ 50%) (both p = 0.023). CMTM6 copy number gain increased CMTM6 expression. Patients with UPS with a high CMTM6 intensity score had a worse prognosis for overall survival. UPS showed variation in CMTM6 copy number and CMTM6 expression. CMTM6 expression was significantly correlated with PD-L1 expression, especially with strong PD-L1 expression.

Details

ISSN :
14321335
Volume :
147
Issue :
7
Database :
OpenAIRE
Journal :
Journal of cancer research and clinical oncology
Accession number :
edsair.doi.dedup.....157188cfdbb0b1d2b84b6f1d831bc673