Systematic Pan-Cancer Analysis of KLRB1 with Prognostic Value and Immunological Activity across Human Tumors

被引:29
作者
Cheng, Xin [1 ]
Cao, Yucheng [2 ]
Wang, Xiaowei [3 ,4 ]
Cheng, Lin [1 ]
Liu, Yaqiong [1 ]
Lei, Jun [1 ]
Peng, Weijun [1 ]
Shi, Dazun [5 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Integrated Tradit Chinese Western Med, Changsha, Peoples R China
[2] Guangzhou Univ Chinese Med, Clin Coll 2, Guangzhou 510006, Guangdong, Peoples R China
[3] Cent South Univ, Xiangya Hosp 2, Dept Pathol, Changsha, Peoples R China
[4] Natl Univ Ireland Galway, Regenerat Med Inst REMEDI, Univ Rd, Galway H91 TK33, Ireland
[5] Cent South Univ, Xiangya Hosp, Dept Gynecol & Obstet, Changsha 410008, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
HUMAN NKR-P1A; T-CELLS; CD161; IMMUNOTHERAPY; RECEPTOR; ACTIVATION; EXPRESSION; LANDSCAPE; MOLECULE; LIGAND;
D O I
10.1155/2022/5254911
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction. KLRB1 is a gene encoding CD161 expressed in NK cells and some T cell subsets. At present, KLRB1 is believed to affect tumorigenesis and development by regulating the cytotoxicity of NK cells in several cancers. However, there is a lack of systematic reviews of KLRB1 in a variety of malignancies. Objectives. Hence, our research is aimed at providing a relatively comprehensive understanding of the role of KLRB1 in different types of cancer, paving the way for further research on the molecular mechanism and immunotherapy potential of KLRB1. Methods. In this study, we used relevant public databases, including TCGA (The Cancer Genome Atlas), GEO (Gene Expression Omnibus), CCLE (Cancer Cell Line Encyclopedia), GTEx (Genotype Tissue-Expression), and HPA (Human Protein Atlas), to perform a pan-cancer analysis of KLRB1 across 33 types of cancer. We explored the potential molecular mechanism of KLRB1 in clinical prognosis and tumor immunity from the aspects of gene expression, survival status, clinical phenotype, immune infiltration, immunotherapy response, and chemotherapeutic drug sensitivity. Results. KLRB1 was downregulated in 13 cancers while upregulated in kidney cancer. Patients with high expression of KLRB1 have a better prognosis in most types of cancer. Moreover, the KLRB1 expression level is related to TMB and MSI and related to various immune signatures of tumor. The expression of KLRB1 can affect tumor immune cell infiltration. KLRB1 expression level can also affect the sensitivity of chemotherapy drugs. Conclusions. KLRB1 may be a prognostic and immunological biomarker across tumors. At the same time, KLRB1 expression can reflect the sensitivity of cancer patients to chemotherapy drugs. KLRB1 may become a new target for immunotherapy.
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页数:21
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共 46 条
[1]   LLT1-mediated Activation of IFN-γ Production in Human Natural Killer Cells Involves ERK Signalling Pathway [J].
Bambard, N. D. ;
Mathew, S. O. ;
Mathew, P. A. .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2010, 71 (03) :210-219
[2]   Immune Landscape of Invasive Ductal Carcinoma Tumor Microenvironment Identifies a Prognostic and Immunotherapeutically Relevant Gene Signature [J].
Bao, Xuanwen ;
Shi, Run ;
Zhang, Kai ;
Xin, Shan ;
Li, Xin ;
Zhao, Yanbo ;
Wang, Yanfang .
FRONTIERS IN ONCOLOGY, 2019, 9
[3]   Expression of LLT1 and its receptor CD161 in lung cancer is associated with better clinical outcome [J].
Braud, Veronique M. ;
Biton, Jerome ;
Becht, Etienne ;
Knockaert, Samantha ;
Mansuet-Lupo, Audrey ;
Cosson, Estelle ;
Damotte, Diane ;
Alifano, Marco ;
Validire, Pierre ;
Anjuere, Fabienne ;
Cremer, Isabelle ;
Girard, Nicolas ;
Gossot, Dominique ;
Seguin-Givelet, Agathe ;
Dieu-Nosjean, Marie-Caroline ;
Germain, Claire .
ONCOIMMUNOLOGY, 2018, 7 (05)
[4]   Mechanisms of Multidrug Resistance in Cancer Chemotherapy [J].
Bukowski, Karol ;
Kciuk, Mateusz ;
Kontek, Renata .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (09)
[5]   Suppression of antitumor T cell immunity by the oncometabolite (R)-2-hydroxyglutarate [J].
Bunse, Lukas ;
Pusch, Stefan ;
Bunse, Theresa ;
Sahm, Felix ;
Sanghvi, Khwab ;
Friedrich, Mirco ;
Alansary, Dalia ;
Sonner, Jana K. ;
Green, Edward ;
Deumelandt, Katrin ;
Kilian, Michael ;
Neftel, Cyril ;
Uhlig, Stefanie ;
Kessler, Tobias ;
von Landenberg, Anna ;
Berghoff, Anna S. ;
Marsh, Kelly ;
Steadman, Mya ;
Zhu, Dongwei ;
Nicolay, Brandon ;
Wiestler, Benedikt ;
Breckwoldt, Michael O. ;
Al-Ali, Ruslan ;
Karcher-Bausch, Simone ;
Bozza, Matthias ;
Oezen, Iris ;
Kramer, Magdalena ;
Meyer, Jochen ;
Habel, Antje ;
Eisel, Jessica ;
Poschet, Gernot ;
Weller, Michael ;
Preusser, Matthias ;
Nadji-Ohl, Minou ;
Thon, Niklas ;
Burger, Michael C. ;
Harter, Patrick N. ;
Ratliff, Miriam ;
Harbottle, Richard ;
Benner, Axel ;
Schrimpf, Daniel ;
Okun, Jurgen ;
Herold-Mende, Christel ;
Turcan, Sevin ;
Kaulfuss, Stefan ;
Hess-Stumpp, Holger ;
Bieback, Karen ;
Cahill, Daniel P. ;
Plate, Karl H. ;
Haenggi, Daniel .
NATURE MEDICINE, 2018, 24 (08) :1192-+
[6]   Sequestration of T cells in bone marrow in the setting of glioblastoma and other intracranial tumors [J].
Chongsathidkiet, Pakawat ;
Jackson, Christina ;
Koyama, Shohei ;
Loebel, Franziska ;
Cui, Xiuyu ;
Farber, S. Harrison ;
Woroniecka, Karolina ;
Elsamadicy, Aladine A. ;
Dechant, Cosette A. ;
Kemeny, Hanna R. ;
Sanchez-Perez, Luis ;
Cheema, Tooba A. ;
Souders, Nicholas C. ;
Herndon, James E. ;
Coumans, Jean-Valery ;
Everitt, Jeffrey, I ;
Nahed, Brian, V ;
Sampson, John H. ;
Gunn, Michael D. ;
Martuza, Robert L. ;
Dranoff, Glenn ;
Curry, William T. ;
Fecci, Peter E. .
NATURE MEDICINE, 2018, 24 (09) :1459-+
[7]   DNA Methyltransferase Inhibitors: Catalysts For Antitumour Immune Responses [J].
Dan, Huimin ;
Zhang, Shanshan ;
Zhou, Yongning ;
Guan, Quanlin .
ONCOTARGETS AND THERAPY, 2019, 12 :10903-10916
[8]   Tertiary lymphoid structures, drivers of the anti-tumor responses in human cancers [J].
Dieu-Nosjean, Marie-Caroline ;
Giraldo, Nicolas A. ;
Kaplon, Helene ;
Germain, Claire ;
Fridman, Wolf Herman ;
Sautes-Fridman, Catherine .
IMMUNOLOGICAL REVIEWS, 2016, 271 (01) :260-275
[9]   The role of myeloid cells in cancer therapies [J].
Engblom, Camilla ;
Pfirschke, Christina ;
Pittet, Mikael J. .
NATURE REVIEWS CANCER, 2016, 16 (07) :447-462
[10]   CD161 (NKR-P1A) costimulation of CD1d-dependent activation of human T cells expressing invariant Vα24JαQ T cell receptorα chains [J].
Exley, M ;
Porcelli, S ;
Furman, M ;
Garcia, J ;
Balk, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (05) :867-876