TIP: A Web Server for Resolving Tumor Immunophenotype Profiling

被引:441
作者
Xu, Liwen [1 ]
Deng, Chunyu [1 ]
Pang, Bo [1 ]
Zhang, Xinxin [1 ]
Liu, Wei [1 ]
Liao, Gaoming [1 ]
Yuan, Huating [1 ]
Cheng, Peng [1 ]
Li, Feng [1 ]
Long, Zhilin [1 ]
Yan, Min [1 ]
Zhao, Tingting [2 ]
Xiao, Yun [1 ]
Li, Xia [1 ]
机构
[1] Harbin Med Univ, Coll Bioinformat Sci & Technol, Harbin 150081, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 1, Dept Neurol, Harbin, Heilongjiang, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金; 国家高技术研究发展计划(863计划);
关键词
EXPRESSION; IMMUNE; REVEALS;
D O I
10.1158/0008-5472.CAN-18-0689
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Systematically tracking the tumor immunophenotype is required to understand the mechanisms of cancer immunity and improve clinical benefit of cancer immunotherapy. However, progress in current research is hindered by the lack of comprehensive immune activity resources and easy-to-use tools for biologists, clinicians, and researchers to conveniently evaluate immune activity during the "cancer-immunity cycle." We developed a user-friendly one-stop shop web tool called TIP to comprehensively resolve tumor immunophenotype. TIP has the capability to rapidly analyze and intuitively visualize the activity of anticancer immunity and the extent of tumor-infiltrating immune cells across the seven-step cancer-immunity cycle. Also, we precalculated the pan-cancer immunophenotype for 11,373 samples from 33 The Cancer Genome Atlas human cancers that allow users to obtain and compare immunophenotype of pan-cancer samples. We expect TIP to be useful in a large number of emerging cancer immunity studies and development of effective immunotherapy biomarkers. TIP is freely available for use at http://biocc.hrbmu.edu.cn/TIP/. Significance: TIP is a one-stop shop platform that can help biologists, clinicians, and researchers conveniently evaluate anticancer immune activity with their own gene expression data. (C) 2018 AACR.
引用
收藏
页码:6575 / 6580
页数:6
相关论文
共 25 条
[21]   Regulatory circuits of T cell function in cancer [J].
Speiser, Daniel E. ;
Ho, Ping-Chih ;
Verdeil, Gregory .
NATURE REVIEWS IMMUNOLOGY, 2016, 16 (10) :500-611
[22]   Statistical and integrative system-level analysis of DNA methylation data [J].
Teschendorff, Andrew E. ;
Relton, Caroline L. .
NATURE REVIEWS GENETICS, 2018, 19 (03) :129-147
[23]   A comparison of reference-based algorithms for correcting cell-type heterogeneity in Epigenome-Wide Association Studies [J].
Teschendorff, Andrew E. ;
Breeze, Charles E. ;
Zheng, Shijie C. ;
Beck, Stephan .
BMC BIOINFORMATICS, 2017, 18
[24]  
Thorsson V, 2019, IMMUNITY, V51, P411, DOI [10.1016/j.immuni.2019.08.004, 10.1016/j.immuni.2018.03.023]
[25]   Quantitative Image Analysis of Cellular Heterogeneity in Breast Tumors Complements Genomic Profiling [J].
Yuan, Yinyin ;
Failmezger, Henrik ;
Rueda, Oscar M. ;
Ali, H. Raza ;
Graef, Stefan ;
Chin, Suet-Feung ;
Schwarz, Roland F. ;
Curtis, Christina ;
Dunning, Mark J. ;
Bardwell, Helen ;
Johnson, Nicola ;
Doyle, Sarah ;
Turashvili, Gulisa ;
Provenzano, Elena ;
Aparicio, Sam ;
Caldas, Carlos ;
Markowetz, Florian .
SCIENCE TRANSLATIONAL MEDICINE, 2012, 4 (157)