Exploring the Genomic Landscape of Hepatobiliary Cancers to Establish a Novel Molecular Classification System.
Anthony J ScholarRebecca K MarcusMary Garland-KledzikDebopriya GhoshMiquel Ensenyat-MendezJoshua GermanyJuan A Santamaria-BarriaAdam KhaderJavier I J OrozcoMelanie GoldfarbPublished in: Cancers (2024)
Taxonomy of hepatobiliary cancer (HBC) categorizes tumors by location or histopathology (tissue of origin, TO). Tumors originating from different TOs can also be grouped by overlapping genomic alterations (GA) into molecular subtypes (MS). The aim of this study was to create novel HBC MSs. Next-generation sequencing (NGS) data from the AACR-GENIE database were used to examine the genomic landscape of HBCs. Machine learning and gene enrichment analysis identified MSs and their oncogenomic pathways. Descriptive statistics were used to compare subtypes and their associations with clinical and molecular variables. Integrative analyses generated three MSs with different oncogenomic pathways independent of TO ( n = 324; p < 0.05). HC-1 "hyper-mutated-proliferative state" MS had rapidly dividing cells susceptible to chemotherapy; HC-2 "adaptive stem cell-cellular senescence" MS had epigenomic alterations to evade immune system and treatment-resistant mechanisms; HC-3 "metabolic-stress pathway" MS had metabolic alterations. The discovery of HBC MSs is the initial step in cancer taxonomy evolution and the incorporation of genomic profiling into the TNM system. The goal is the development of a precision oncology machine learning algorithm to guide treatment planning and improve HBC outcomes. Future studies should validate findings of this study, incorporate clinical outcomes, and compare the MS classification to the AJCC 8th staging system.
Keyphrases
- machine learning
- mass spectrometry
- copy number
- multiple sclerosis
- ms ms
- stem cells
- papillary thyroid
- pet ct
- big data
- single cell
- artificial intelligence
- emergency department
- induced apoptosis
- small molecule
- endothelial cells
- squamous cell carcinoma
- electronic health record
- adipose tissue
- palliative care
- dna methylation
- single molecule
- cell proliferation
- gene expression
- rectal cancer
- locally advanced
- bone marrow
- childhood cancer
- high throughput
- metabolic syndrome
- stress induced
- cell therapy
- cell cycle arrest
- pi k akt
- young adults
- oxidative stress
- heat stress
- weight loss