Comprehensive Benchmarking and Integration of Tumor Microenvironment Cell Estimation Methods.
Alejandro Jiménez-SánchezOliver CastMartin L MillerPublished in: Cancer research (2019)
Various computational approaches have been developed for estimating the relative abundance of different cell types in the tumor microenvironment (TME) using bulk tumor RNA data. However, a comprehensive comparison across diverse datasets that objectively evaluates the performance of these approaches has not been conducted. Here, we benchmarked seven widely used tools and gene sets and introduced ConsensusTME, a method that integrates gene sets from all the other methods for relative TME cell estimation of 18 cell types. We collected a comprehensive benchmark dataset consisting of pan-cancer data (DNA-derived purity, leukocyte methylation, and hematoxylin and eosin-derived lymphocyte counts) and cell-specific benchmark datasets (peripheral blood cells and tumor tissues). Although none of the methods outperformed others in every benchmark, ConsensusTME ranked top three in all cancer-related benchmarks and was the best performing tool overall. We provide a Web resource to interactively explore the benchmark results and an objective evaluation to help researchers select the most robust and accurate method to further investigate the role of the TME in cancer (www.consensusTME.org). SIGNIFICANCE: This work shows an independent and comprehensive benchmarking of recently developed and widely used tumor microenvironment cell estimation methods based on bulk expression data and integrates the tools into a consensus approach.
Keyphrases
- single cell
- peripheral blood
- cell therapy
- rna seq
- gene expression
- dna methylation
- physical activity
- poor prognosis
- machine learning
- electronic health record
- microbial community
- young adults
- induced apoptosis
- papillary thyroid
- bone marrow
- transcription factor
- lymph node metastasis
- cell free
- cell cycle arrest
- childhood cancer