Best Practices for Spatial Profiling for Breast Cancer Research with the GeoMx(R) Digital Spatial Profiler

被引:68
作者
Bergholtz, Helga [1 ]
Carter, Jodi M. [2 ]
Cesano, Alessandra [3 ]
Cheang, Maggie Chon U. [4 ]
Church, Sarah E. [5 ]
Divakar, Prajan [5 ]
Fuhrman, Christopher A. [5 ]
Goel, Shom [6 ,7 ]
Gong, Jingjing [5 ]
Guerriero, Jennifer L. [8 ]
Hoang, Margaret L. [5 ]
Hwang, E. Shelley [9 ]
Kuasne, Hellen [10 ]
Lee, Jinho [11 ]
Liang, Yan [5 ]
Mittendorf, Elizabeth A. [8 ,12 ,13 ]
Perez, Jessica [5 ]
Prat, Aleix [14 ]
Pusztai, Lajos [15 ]
Reeves, Jason W. [5 ]
Riazalhosseini, Yasser [16 ,17 ]
Richer, Jennifer K. [18 ]
Sahin, Ozgur [19 ]
Sato, Hiromi [5 ]
Schlam, Ilana [20 ,21 ]
Sorlie, Therese [1 ,22 ]
Stover, Daniel G. [23 ]
Swain, Sandra M. [24 ,25 ,26 ]
Swarbrick, Alexander [27 ,28 ]
Thompson, E. Aubrey [29 ]
Tolaney, Sara M. [13 ,30 ]
Warren, Sarah E. [5 ]
机构
[1] Oslo Univ Hosp, Inst Canc Res, Dept Canc Genet, N-0450 Oslo, Norway
[2] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[3] ESSA Pharma Inc, San Francisco, CA 94080 USA
[4] Inst Canc Res, Div Clin Studies, ICR Clin Trials & Stat Unit, London SM2 5NG, England
[5] NanoString Technol Inc, Seattle, WA 98109 USA
[6] Peter MacCallum Canc Ctr, Melbourne, Vic 3000, Australia
[7] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Parkville, Vic 3010, Australia
[8] Brigham & Womens Hosp, Dept Surg, Div Breast Surg, Boston, MA 02115 USA
[9] Duke Univ, Duke Canc Inst, Durham, NC 27710 USA
[10] McGill Univ, Rosalind & Morris Goodman Canc Ctr, Montreal, PQ H3A 0G4, Canada
[11] Oregon Hlth & Sci Univ, Knight Canc Inst, Portland, OR 97239 USA
[12] Dana Farber Canc Inst, Breast Oncol Program, Boston, MA 02215 USA
[13] Harvard Med Sch, Boston, MA 02115 USA
[14] August Pi & Sunyer Biomed Res Inst, Translat Genom & Targeted Therapies Solid Tumors, Barcelona 08036, Spain
[15] Yale Sch Med, Yale Canc Ctr, New Haven, CT 06510 USA
[16] McGill Univ, Dept Human Genet, Montreal, PQ H3A 0G4, Canada
[17] McGill Univ, McGill Univ Genome Ctr, Montreal, PQ H3A 0G4, Canada
[18] Univ Colorado, Dept Pathol, Anschutz Med Campus, Aurora, CO 80045 USA
[19] Univ South Carolina, Dept Drug Discovery & Biomed Sci, Columbia, SC 29208 USA
[20] MedStar Washington Hosp Ctr, Washington, DC 20010 USA
[21] Tufts Med Ctr, Boston, MA 02111 USA
[22] Univ Oslo, Inst Clin Med, N-0315 Oslo, Norway
[23] Ohio State Univ, Comprehens Canc Ctr, Columbus, OH 43210 USA
[24] Georgetown Lombardi Comprehens Canc Ctr, Washington, DC 20057 USA
[25] Georgetown Univ, Med Ctr, Washington, DC 20057 USA
[26] MedStar Hlth, Washington, DC 20057 USA
[27] Garvan Inst Med Res, Darlinghurst, NSW 2010, Australia
[28] UNSW Sydney, Fac Med, St Vincents Clin Sch, Sydney 2052, Australia
[29] Mayo Clin Florida, Dept Canc Biol, Jacksonville, FL 32224 USA
[30] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
关键词
breast cancer; spatial biology; RNA and protein profiling; GeoMx; digital spatial profiler; tumor microenvironment; biomarker discovery; whole transcriptome atlas; cancer transcriptome atlas; tumor heterogeneity; TUMOR-INFILTRATING LYMPHOCYTES; INTRATUMOR HETEROGENEITY; T-CELLS; EXPRESSION; RECEPTOR; RNA; IMMUNOTHERAPY; CHEMOTHERAPY; MULTIPLEX; BIOMARKER;
D O I
10.3390/cancers13174456
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary In breast cancer, there is a high degree of variability in tumors and the surrounding tissue called the tumor microenvironment (TME). To better understand tumor biology and metastasis, as well as to predict response to cancer treatments or the course of the disease, it is important to characterize molecular diversity in the breast TME. The GeoMx Digital Spatial Profiler (DSP) enables researchers to spatially analyze proteins and RNA transcripts in tumors and surrounding tissues from patients or preclinical models. Using the GeoMx DSP, protein expression and RNA transcripts in the distinct regions of a tumor can be quantified up to and including the whole transcriptome level. Herein, the GeoMx Breast Cancer Consortium presents best practices for GeoMx spatial profiling of tumors to promote the collection of high-quality data, optimization of data analysis and integration of datasets to accelerate biomarker discovery. These best practices can also be applied to any tumor type to provide information about the tumor and the TME. Breast cancer is a heterogenous disease with variability in tumor cells and in the surrounding tumor microenvironment (TME). Understanding the molecular diversity in breast cancer is critical for improving prediction of therapeutic response and prognostication. High-plex spatial profiling of tumors enables characterization of heterogeneity in the breast TME, which can holistically illuminate the biology of tumor growth, dissemination and, ultimately, response to therapy. The GeoMx Digital Spatial Profiler (DSP) enables researchers to spatially resolve and quantify proteins and RNA transcripts from tissue sections. The platform is compatible with both formalin-fixed paraffin-embedded and frozen tissues. RNA profiling was developed at the whole transcriptome level for human and mouse samples and protein profiling of 100-plex for human samples. Tissue can be optically segmented for analysis of regions of interest or cell populations to study biology-directed tissue characterization. The GeoMx Breast Cancer Consortium (GBCC) is composed of breast cancer researchers who are developing innovative approaches for spatial profiling to accelerate biomarker discovery. Here, the GBCC presents best practices for GeoMx profiling to promote the collection of high-quality data, optimization of data analysis and integration of datasets to advance collaboration and meta-analyses. Although the capabilities of the platform are presented in the context of breast cancer research, they can be generalized to a variety of other tumor types that are characterized by high heterogeneity.
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页数:27
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