التفاصيل البيبلوغرافية
العنوان: |
Ultra High‐Plex Spatial Proteogenomic Investigation of Giant Cell Glioblastoma Multiforme Immune Infiltrates Reveals Distinct Protein and RNA Expression Profiles |
المؤلفون: |
Bonnett, Shilah, Rosenbloom, Alyssa, Ong, Giang, Conner, Mark, Newhouse, Daniel, New, Felicia, Sato, Hiromi, Phan, Chi, Ilcisin, Saskia, Lyssand, John, Geiss, Gary, Beechem, Joseph M. |
المصدر: |
Alzheimer's & Dementia ; volume 19, issue S13 ; ISSN 1552-5260 1552-5279 |
بيانات النشر: |
Wiley |
سنة النشر: |
2023 |
المجموعة: |
Wiley Online Library (Open Access Articles via Crossref) |
الوصف: |
Background The advancement of spatially resolved, multiplex proteomic and transcriptomic technologies has revolutionized and redefined the approaches to complex biological questions pertaining to tissue heterogeneity, tumor microenvironments, cellular interactions, cellular diversity, and therapeutic response. Most spatial technologies yield single analyte proteomic or transcriptomic datasets from separate formalin‐fixed paraffin‐embedded (FFPE) tissues sections. Multiple studies have demonstrated a poor correlation between RNA expression and protein abundance owing to transcriptional and translational regulation, target turnover, and post‐translational protein modifications. Therefore, a workflow that accurately measures RNA and protein simultaneously within a single tissue section with distinct spatial context is critical to a more complete biological understanding of cellular interactions and activities. Such multimodal omic datasets of protein and DNA or RNA have been termed “spatial proteogenomics”. Method Here we present a novel spatial proteogenomic (SPG) assay on the GeoMx ® Digital Spatial Profiler platform with NGS readout that enables ultra high‐plex digital quantitation of proteins (147‐plex) and RNA (whole transcriptome,>18,000‐plex) from a single FFPE sample. We demonstrated high concordance, R>0.85, and minor change in sensitivity (<11%) between the SPG assay and the single analyte GeoMx Whole Transcriptome Atlas and GeoMx NGS Protein assays. We used the SPG assay to interrogate 23 different glioblastoma multiforme samples across 4 pathologies. Results We observed clustering of both RNA and protein based on cancer pathology and anatomic location. The in‐depth investigation of giant cell glioblastoma multiforme (gcGBM) revealed distinct protein and RNA expression profiles compared to that of glioblastoma multiforme (GBM). Spatial proteogenomics allowed simultaneous interrogation of critical protein post‐translational modifications alongside whole transcriptomic profiles within the ... |
نوع الوثيقة: |
article in journal/newspaper |
اللغة: |
English |
DOI: |
10.1002/alz.076769 |
الاتاحة: |
http://dx.doi.org/10.1002/alz.076769 |
Rights: |
http://onlinelibrary.wiley.com/termsAndConditions#vor |
رقم الانضمام: |
edsbas.5CD523C6 |
قاعدة البيانات: |
BASE |