Ontology highlight
ABSTRACT: Background
Cell free RNA (cfRNA) contains transcript fragments from multiple cell types, making it useful for cancer detection in clinical settings. However, the pathophysiological origins of cfRNAs in plasma from colorectal cancer (CRC) patients remain unclear.Methods
To identify the tissue-specific contributions of cfRNAs transcriptomic profile, we used a published single-cell transcriptomics profile to deconvolute cell type abundance among paired plasma samples from CRC patients who underwent tumor-ablative surgery. We further validated the differentially expressed cfRNAs in 5 pairs of CRC tumor samples and adjacent tissue samples as well as 3 additional CRC tumor samples using RNA-sequencing.Results
The transcriptomic component from intestinal secretory cells was significantly decreased in the in-house post-surgical cfRNA. The HPGD, PACS1, and TDP2 expression was consistent across cfRNA and tissue samples. Using the Cancer Genome Atlas (TCGA) CRC datasets, we were able to classify the patients into two groups with significantly different survival outcomes.Conclusions
The three-gene signature holds promise in applying minimal residual disease (MRD) testing, which involves profiling remnants of cancer cells after or during treatment. Biomarkers identified in the present study need to be validated in a larger cohort of samples in order to ascertain their possible use in early diagnosis of CRC.
SUBMITTER: Jin N
PROVIDER: S-EPMC10115432 | biostudies-literature | 2023
REPOSITORIES: biostudies-literature
Jin Nana N Kan Chau-Ming CM Pei Xiao Meng XM Cheung Wing Lam WL Ng Simon Siu Man SSM Wong Heong Ting HT Cheng Hennie Yuk-Lin HY Leung Wing Wa WW Wong Yee Ni YN Tsang Hin Fung HF Chan Amanda Kit Ching AKC Wong Yin Kwan Evelyn YKE Cho William Chi Shing WCS Chan John Kwok Cheung JKC Tai William Chi Shing WCS Chan Ting-Fung TF Wong Sze Chuen Cesar SCC Yim Aldrin Kay-Yuen AK Yu Allen Chi-Shing AC
Frontiers in oncology 20230405
<h4>Background</h4>Cell free RNA (cfRNA) contains transcript fragments from multiple cell types, making it useful for cancer detection in clinical settings. However, the pathophysiological origins of cfRNAs in plasma from colorectal cancer (CRC) patients remain unclear.<h4>Methods</h4>To identify the tissue-specific contributions of cfRNAs transcriptomic profile, we used a published single-cell transcriptomics profile to deconvolute cell type abundance among paired plasma samples from CRC patien ...[more]