nCounter® Breast Cancer 360™ Panel

Helping Your Research

Want a system that provides a unique 360° view of gene expression for the breast tumor, microenvironment, and immune response? If yes, then you have found the right product. The Human nCounter Breast Cancer 360 panel and data analysis report helps researchers quickly decode the complexities of breast cancer biology, develop novel breast cancer gene signatures, and categorize disease heterogeneity using 48 biological signatures including signatures based upon the validated PAM50 and Tumor Inflammation Signature (TIS) assays. Get the most out of your panel by quickly distilling a large amount of data into actionable signatures measuring variables crucial to breast tumor-immune interaction.

Inspired by systems biology approaches to cancer research, NanoString’s 360 Series Panel Collection gives you a 360° view of gene expression by combining carefully-curated content involved in the biology of the tumor, microenvironment, and the immune response into a single holistic assay. Each panel contains the 18-gene Tumor Inflammation Signature (TIS) that measures a peripherally-suppressed, adaptive immune response and has been shown to correlate with response to checkpoint inhibitors.

Breast Cancer

How It Works

The content included in the Breast Cancer 360 panel allows for a more comprehensive measurement of biological variables crucial to tumor progression and response to a wide range of treatments. Research signatures are enriched with potentially predictive genes involved in proliferation, endothelium, angiogenesis, cytotoxicity, stroma, inflammatory chemokines, and apoptosis.
01:

Highly Curated Content:

Expertly curated, comprehensive content includes 776 genes across 23 key breast cancer pathways and processes, 10 research focused signatures and 30 novel signatures measuring important tumor and immune activities.

02:

Comprehensive Coverage:

Expanded evaluation of breast cancer subtypes including: PAM50 Signature, TNBC, and Claudin-Low Signature.

03:

Interactive, Flexible Report:

The Interactive Breast Cancer 360 data analysis report provides insight into 48 signatures across 13 categories measuring biological variables crucial to breast cancer tumor biology.

You can access validated signatures like PAM50, Tumor Inflammation Signature (TIS), Risk of Recurrence (ROR)/Genomic Risk. Analyze your data by survival, response or grouping variables, or drill down into individual sample variability. Analyze clinical variables by TNBC/PAM50 subtype or variables of your choosing.

04:

Publication-Ready Data:

The report generates figures, statistical outputs, and methods for your publication or poster presentation.

Panel Selection Tool

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Product Information

Breast Cancer 360 Biological Signatures
Breast Cancer 360 Pathways and Processes
PAM50 and TIS Signatures
Product Specifications
Product Comparison
Catalog Information
Breast Cancer 360 Biological Signatures
Breast Cancer 360 Pathways and Processes

Includes expertly curated 776 genes across 23 categories of breast cancer tumor biology to support the evaluation of pathways and process, as well as novel signature development.

PAM50 and TIS Signatures

Content included in the Breast Cancer 360 panel allows for a more comprehensive measurement of biological variables crucial to tumor progression and response to a wide range of treatments. Research signatures are enriched with potentially predictive genes involved in proliferation, endothelium, angiogenesis, cytotoxicity, stroma, inflammatory chemokines, and apoptosis.

  • 48 signatures including two analytically validated signatures- PAM50 and Tumor Inflammation Signature
  • 10 research-focused signatures and 30 novel signatures measuring important tumor and immune activities
  • adapted to decode breast cancer biology in concert

Analytically Validated Signatures

PAM50 Signature1,2

Included with the Breast Cancer 360 panel is the PAM50 Signature.  This 50-gene signature measures a gene expression profile that allows for the classification of breast cancer into four biologically distinct subtypes and a prognostic score.

  • PAM50 Subtype
    • Luminal A
    • Luminal B
    • HER2-Enriched
    • Basal-like
  • Prosigna Score / Risk of Recurrence

Tumor Inflammation Signature3

Included with the Breast Cancer 360 panel is the Tumor Inflammation Signature. This 18-gene signature measures activity known to be associated with response to PD-1/PD-L1 inhibitors pathway blockade3.

  • Includes 4 areas of immune biology used to determine peripherally suppressed immune response and the identification of “hot” or “cold” tumors
    • Antigen Presenting Cells
    • T Cell/NK presence
    • IFNγ Biology
    • T Cell Exhaustion
  • Tissue-of-origin agnostic (Pan-cancer)
  • Potential surrogate for PD-L1 and mutational load in research setting4

View publication and video.

Product Specifications
Product Comparison

360 Series Product Comparison

Fully-annotated gene lists in Excel format are available for each of the 360 Panels. The table below compares the biology coverage of the 360 Panels across the tumor, microenvironment, and the immune response to that of the PanCancer Panels Collection.

Catalog Information

Related Resources

See All Resources
Product Bulletin Breast Cancer 360 – Product Bulletin
Report BC360 Demo Data Analysis Report
Report BC360 Time Series Demo Data Analysis Report
Report BC360 TNBC Demo Data Analysis Report
Report Viewing nCounter 360 Web Reports

Publications

View All Publications

Highly Multiplexed Spatially Resolved Proteomic and Transcriptional Profiling of the Glioblastoma Microenvironment Using Archived Formalin-Fixed Paraffin-Embedded Specimens.

Glioblastoma is a heterogeneous tumor for which effective treatment options are limited and often insufficient. Few studies have examined the intratumoral transcriptional and proteomic heterogeneity of the glioblastoma microenvironment to characterize the spatial distribution of potential molecular and cellular therapeutic immunooncology targets.

PFKFB3 overexpression in monocytes of patients with colon but not rectal cancer programs pro-tumor macrophages and is indicative for higher risk of tumor relapse.

Introduction: Circulating monocytes are main source for tumor-associated macrophages (TAMs) that control tumor growth, angiogenesis, metastasis and therapy resistance. We raised the questions how monocyte programming is affected by growing tumors localized in colon and rectal sections, and how treatment onsets affect monocyte programming in the circulation.

Spatial genomics reveals a high number and specific location of B cells in the pancreatic ductal adenocarcinoma microenvironment of long-term survivors.

Background and aim: Only 10% of pancreatic ductal adenocarcinoma (PDAC) patients survive longer than five years. Factors underlining long-term survivorship in PDAC are not well understood.

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