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pmid:37509213

Assessment of Colorectal Cancer Risk Factors through the Application of Network-Based Approaches in a Racially Diverse Cohort of Colon Organoid Stem Cells.

Matthew Devall · Stephen Eaton · Cynthia Yoshida · Steven M Powell · Graham Casey · Li Li

Cancers · 2023 doi:10.3390/cancers15143550

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Assessment of Colorectal Cancer Risk Factors through the Application of Network-Based Approaches in a Racially Diverse Cohort of Colon Organoid Stem Cells.
doi
10.3390/cancers15143550
pmid
37509213
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Matthew Devall
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Stephen Eaton
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Cynthia Yoshida
[3]
Steven M Powell
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Graham Casey
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Li Li
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Cancers
year
2023
abstract
Numerous demographic factors have been associated with colorectal cancer (CRC) risk. To better define biological mechanisms underlying these associations, we performed RNA sequencing of stem-cell-enriched organoids derived from the healthy colons of seven European Americans and eight African Americans. A weighted gene co-expression network analysis was performed following RNA sequencing. Module-trait relationships were determined through the association testing of each module and five CRC risk factors (age, body mass index, sex, smoking history, and race). Only modules that displayed a significantly positive correlation for gene significance and module membership were considered for further investigation. In total, 16 modules were associated with known CRC risk factors (p < 0.05). To contextualize the role of risk modules in CRC, publicly available RNA-sequencing data from TCGA-COAD were downloaded and re-analyzed. Differentially expressed genes identified between tumors and matched normal-adjacent tissue were overlaid across each module. Loci derived from CRC genome-wide association studies were additionally overlaid across modules to identify robust putative targets of risk. Among them, MYBL2 and RXRA represented strong plausible drivers through which cigarette smoking and BMI potentially modulated CRC risk, respectively. In summary, our findings highlight the potential of the colon organoid system in identifying novel CRC risk mechanisms in an ancestrally diverse and cellularly relevant population.
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Assessment of colorectal cancer risk factors through the application of network-based approaches in a biracial cohort of colon organoid stem cells
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e of risk modules in CRC, publicly available RNA-sequencing data from TCGA-COAD were downloaded and re-a
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underlying these associations, we performed RNA sequencing of stem-cell-enriched organoids derived from
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Complete file
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