Polymorphisms of the PD-L1 gene 3′-untranslated region are associated with the expression of PD-L1 in non-small cell lung cancer

被引:1
作者
Ohhara, Yoshihito [1 ,2 ]
Tomaru, Utano [3 ,9 ]
Kinoshita, Ichiro [1 ,2 ,4 ]
Hatanaka, Kanako C. [5 ,6 ]
Noguchi, Takuro [1 ,2 ]
Hatanaka, Yutaka [5 ]
Amono, Toraji [7 ]
Matsuno, Yoshihiro [3 ]
Dosaka-Akita, Hirotoshi [1 ,2 ,8 ]
机构
[1] Hokkaido Univ, Fac Med, Dept Med Oncol, Sapporo, Japan
[2] Hokkaido Univ, Grad Sch Med, Sapporo, Japan
[3] Hokkaido Univ Hosp, Dept Surg Pathol, Sapporo, Japan
[4] Hokkaido Univ Hosp, Div Clin Canc Genom, Sapporo, Japan
[5] Hokkaido Univ Hosp, Res Div Genome Compan Diagnost, Sapporo, Japan
[6] Hokkaido Univ Hosp, Ctr Dev Adv Diagnost, Sapporo, Japan
[7] Hokkaido Univ Hosp, Clin Res & Med Innovat Ctr, Sapporo, Japan
[8] Hokkaido Univ Hosp, Res Div Canc Immunotherapy, Sapporo, Japan
[9] Hokkaido Univ Hosp, Dept Surg Pathol, Kita 14 Nishi 5,Kita Ku, Sapporo 0608648, Japan
关键词
3'-UTR; microRNA; non-small cell lung cancers; PD-L1; single-nucleotide polymorphism; PROGNOSIS; B7-H1; TUMOR;
D O I
10.1002/gcc.23216
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent results show that polymorphisms of programmed death ligand 1 (PD-L1, also known as CD274 or B7-H1) might be used as a possible marker for effectiveness of chemotherapy and cancer risk. However, the effect of PD-L1 gene variations on PD-L1 expression remain unclear. Given the post-transcriptional machinery in tumor PD-L1 expression, we investigated single nucleotide polymorphisms (SNPs) in the 3 '-untranslated region (3 '-UTR) of the PD-L1 gene, rs4143815 and rs4742098, using formalin-fixed paraffin-embedded sections of 154 patients with non-small cell lung cancers (NSCLCs). In rs4143815, the GG genotype showed significant association with PD-L1 expression (P = 0.032). In rs4742098, the AA genotype was significantly associated with histology and PD-L1 expression (P = 0.022 and P = 0.008, respectively). In multivariate logistic regression analysis, the AA genotype in rs4742098 was correlated with PD-L1 expression (odds ratio 0.408, P = 0.048). Interestingly, approximately 10% of the NSCLC cases showed somatic mutation when we compared genotypes of these SNPs between NSCLC tissues and non-tumor tissues from the same patients. In addition, cases with somatic mutation showed higher levels of PD-L1 expression than cases with germline mutation in rs4143815 GG. In conclusion, we demonstrated that the rs4143815 and rs4742098 SNPs in the 3 '-UTR of PD-L1 were associated with tumor PD-L1 expression in NSCLCs.
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页数:9
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共 32 条
[1]   Investigation of single and synergic effects of NLRC5 and PD-L1 variants on the risk of colorectal cancer [J].
Catalano, Calogerina ;
da Silva Filho, Miguel Inacio ;
Frank, Christoph ;
Jiraskova, Katerina ;
Vymetalkova, Veronika ;
Levy, Miroslav ;
Liska, Vaclav ;
Vycital, Ondrej ;
Naccarati, Alessio ;
Vodickova, Ludmila ;
Hemminki, Kari ;
Vodicka, Pavel ;
Weber, Alexander N. R. ;
Foersti, Asta .
PLOS ONE, 2018, 13 (02)
[2]   Metastasis is regulated via microRNA-200/ZEB1 axis control of tumour cell PD-L1 expression and intratumoral immunosuppression [J].
Chen, Limo ;
Gibbons, Don L. ;
Goswami, Sangeeta ;
Cortez, Maria Angelica ;
Ahn, Young-Ho ;
Byers, Lauren A. ;
Zhang, Xuejun ;
Yi, Xiaohui ;
Dwyer, David ;
Lin, Wei ;
Diao, Lixia ;
Wang, Jing ;
Roybal, Jonathon D. ;
Patel, Mayuri ;
Ungewiss, Christin ;
Peng, David ;
Antonia, Scott ;
Mediavilla-Varela, Melanie ;
Robertson, Gordon ;
Jones, Steve ;
Suraokar, Milind ;
Welsh, James W. ;
Erez, Baruch ;
Wistuba, Ignacio I. ;
Chen, Lieping ;
Peng, Di ;
Wang, Shanshan ;
Ullrich, Stephen E. ;
Heymach, John V. ;
Kurie, Jonathan M. ;
Qin, F. Xiao-Feng .
NATURE COMMUNICATIONS, 2014, 5
[3]   Immune checkpoint inhibitors for nonsmall cell lung cancer treatment [J].
Chen, Yuh-Min .
JOURNAL OF THE CHINESE MEDICAL ASSOCIATION, 2017, 80 (01) :7-14
[4]  
Dong HD, 2002, NAT MED, V8, P793, DOI 10.1038/nm730
[5]   Variant SNPs at the microRNA complementary site in the B7-H1 3'-untranslated region increase the risk of non-small cell lung cancer [J].
Du, Wenwen ;
Zhu, Jianjie ;
Chen, Yanbin ;
Zeng, Yuanyuan ;
Shen, Dan ;
Zhang, Nan ;
Ning, Weiwei ;
Liu, Zeyi ;
Huang, Jian-An .
MOLECULAR MEDICINE REPORTS, 2017, 16 (03) :2682-2690
[6]   The IASLC Lung Cancer Staging Project: Proposals for Revision of the TNM Stage Groupings in the Forthcoming (Eighth) Edition of the TNM Classification for Lung Cancer [J].
Goldstraw, Peter ;
Chansky, Kari ;
Crowley, John ;
Rami-Porta, Ramon ;
Asamura, Hisao ;
Eberhardt, Wilfried E. E. ;
Nicholson, Andrew G. ;
Groome, Patti ;
Mitchell, Alan ;
Bolejack, Vanessa .
JOURNAL OF THORACIC ONCOLOGY, 2016, 11 (01) :39-51
[7]   Atezolizumab for First-Line Treatment of PD-L1-Selected Patients with NSCLC [J].
Herbst, Roy S. ;
Giaccone, Giuseppe ;
de Marinis, Filippo ;
Reinmuth, Niels ;
Vergnenegre, Alain ;
Barrios, Carlos H. ;
Morise, Masahiro ;
Felip, Enriqueta ;
Andric, Zoran ;
Geater, Sarayut ;
Ozguroglu, Mustafa ;
Zou, Wei ;
Sandler, Alan ;
Enquist, Ida ;
Komatsubara, Kimberly ;
Deng, Yu ;
Kuriki, Hiroshi ;
Wen, Xiaohui ;
McCleland, Mark ;
Mocci, Simonetta ;
Jassem, Jacek ;
Spigel, David R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2020, 383 (14) :1328-1339
[8]   New and emerging targeted treatments in advanced non-small-cell lung cancer [J].
Hirsch, Fred R. ;
Suda, Kenichi ;
Wiens, Jacinta ;
Bunn, Paul A., Jr. .
LANCET, 2016, 388 (10048) :1012-1024
[9]   Expression of Fucosyltransferase 8 Is Associated with an Unfavorable Clinical Outcome in Non-Small Cell Lung Cancers [J].
Honma, Rio ;
Kinoshita, Ichiro ;
Miyoshi, Eiji ;
Tomaru, Utano ;
Matsuno, Yoshihiro ;
Shimizu, Yasushi ;
Takeuchi, Satoshi ;
Kobayashi, Yuka ;
Kaga, Kichizo ;
Taniguchi, Naoyuki ;
Dosaka-Akita, Hirotoshi .
ONCOLOGY, 2015, 88 (05) :298-308
[10]   Aberrant PD-L1 expression through 3′-UTR disruption in multiple cancers [J].
Kataoka, Keisuke ;
Shiraishi, Yuichi ;
Takeda, Yohei ;
Sakata, Seiji ;
Matsumoto, Misako ;
Nagano, Seiji ;
Maeda, Takuya ;
Nagata, Yasunobu ;
Kitanaka, Akira ;
Mizuno, Seiya ;
Tanaka, Hiroko ;
Chiba, Kenichi ;
Ito, Satoshi ;
Watatani, Yosaku ;
Kakiuchi, Nobuyuki ;
Suzuki, Hiromichi ;
Yoshizato, Tetsuichi ;
Yoshida, Kenichi ;
Sanada, Masashi ;
Itonaga, Hidehiro ;
Imaizumi, Yoshitaka ;
Totoki, Yasushi ;
Munakata, Wataru ;
Nakamura, Hiromi ;
Hama, Natsuko ;
Shide, Kotaro ;
Kubuki, Yoko ;
Hidaka, Tomonori ;
Kameda, Takuro ;
Masuda, Kyoko ;
Minato, Nagahiro ;
Kashiwase, Koichi ;
Izutsu, Koji ;
Takaori-Kondo, Akifumi ;
Miyazaki, Yasushi ;
Takahashi, Satoru ;
Shibata, Tatsuhiro ;
Kawamoto, Hiroshi ;
Akatsuka, Yoshiki ;
Shimoda, Kazuya ;
Takeuchi, Kengo ;
Seya, Tsukasa ;
Miyano, Satoru ;
Ogawa, Seishi .
NATURE, 2016, 534 (7607) :402-+