Matches in SemOpenAlex for { <https://semopenalex.org/work/W3187378970> ?p ?o ?g. }
- W3187378970 endingPage "115657" @default.
- W3187378970 startingPage "115657" @default.
- W3187378970 abstract "Colorectal cancer (CRC) remains a major concern with high morbidity and mortality worldwide. Despite the positive influence of chemotherapy on the decline in CRC mortality, the negative influence of chemotherapy-related adverse effects (CRAEs) caused by capecitabine (Cap) remains a challenging problem. DNA methylation alteration plays a pivotal role in gene expression regulation. Here, we aimed to screen reliable and novel biomarkers for CRC diagnosis and CRAE prediction using the advanced Illumina Infinium MethylationEPIC (850 K) BeadChip. Paired tumor and normal tissues from 21 Chinese CRC patients who received Cap-based adjuvant chemotherapy were analyzed. CRC-related methylation was characterized by hypermethylated promoter islands and hypomethylated intragenic openseas; CRAE-related methylation was characterized by hyper- (or hypo-) methylated intragenic (or intergenic) regions. Based on three types of methylation profiles (differentially methylated probes, differentially methylated regions, and gene-function-differentially methylated regions), pathway enrichment analyses revealed that CRC-related genes were significantly enriched in the neuronal system, metabolism of RNA, and extracellular matrix organization; CRAE-related genes were abundantly enriched in pathways controlling regeneration functions and immune response. Finally, based on genes within the mostly related pathways and LASSO logistic regression selection, the integrated-methylation-marker systems developed here demonstrated high discriminative accuracy in both CRC diagnosis (AUROC = 1) and CRAE prediction (AUROC = 0.817–1). In conclusion, we conducted a comprehensive DNA methylation analysis of CRC patients with chemotherapy, which provided new insights into the formation of CRC and CRAEs. Most importantly, our findings identified potentially CRAE-related metabolic pathways and markers, providing a valuable reference for personalized medicine promising better safety. Trail registration: ClinicalTrials.gov , NCT03030508 , Registered 25 January 2017, https://www.clinicaltrials.gov/ct2/show/NCT03030508?term=NCT03030508&draw=2&rank=1 ." @default.
- W3187378970 created "2021-08-16" @default.
- W3187378970 creator A5000470216 @default.
- W3187378970 creator A5013951309 @default.
- W3187378970 creator A5024857104 @default.
- W3187378970 creator A5027024463 @default.
- W3187378970 creator A5033846884 @default.
- W3187378970 creator A5040423679 @default.
- W3187378970 creator A5045557806 @default.
- W3187378970 creator A5060708223 @default.
- W3187378970 creator A5070512804 @default.
- W3187378970 creator A5070863871 @default.
- W3187378970 creator A5074752067 @default.
- W3187378970 creator A5079759848 @default.
- W3187378970 date "2021-09-01" @default.
- W3187378970 modified "2023-09-24" @default.
- W3187378970 title "Genomic methylation variations predict the susceptibility of six chemotherapy related adverse effects and cancer development for Chinese colorectal cancer patients" @default.
- W3187378970 cites W1546909751 @default.
- W3187378970 cites W1576005490 @default.
- W3187378970 cites W1599313687 @default.
- W3187378970 cites W1612816801 @default.
- W3187378970 cites W1639623904 @default.
- W3187378970 cites W1965167394 @default.
- W3187378970 cites W1965914119 @default.
- W3187378970 cites W1974747095 @default.
- W3187378970 cites W1977064103 @default.
- W3187378970 cites W1979186680 @default.
- W3187378970 cites W1981705797 @default.
- W3187378970 cites W1982217924 @default.
- W3187378970 cites W1982987383 @default.
- W3187378970 cites W1988028386 @default.
- W3187378970 cites W1988475719 @default.
- W3187378970 cites W1998918372 @default.
- W3187378970 cites W2022711719 @default.
- W3187378970 cites W2023295503 @default.
- W3187378970 cites W2027229185 @default.
- W3187378970 cites W2043661964 @default.
- W3187378970 cites W2054863651 @default.
- W3187378970 cites W2056664397 @default.
- W3187378970 cites W2056668463 @default.
- W3187378970 cites W2065057589 @default.
- W3187378970 cites W2065253498 @default.
- W3187378970 cites W2066321163 @default.
- W3187378970 cites W2074017816 @default.
- W3187378970 cites W2085213378 @default.
- W3187378970 cites W2089473025 @default.
- W3187378970 cites W2093223492 @default.
- W3187378970 cites W2100382861 @default.
- W3187378970 cites W2101007892 @default.
- W3187378970 cites W2103441770 @default.
- W3187378970 cites W2108797218 @default.
- W3187378970 cites W2131474316 @default.
- W3187378970 cites W2135498562 @default.
- W3187378970 cites W2140099805 @default.
- W3187378970 cites W2141923938 @default.
- W3187378970 cites W2142827726 @default.
- W3187378970 cites W2148521032 @default.
- W3187378970 cites W2149236738 @default.
- W3187378970 cites W2149894474 @default.
- W3187378970 cites W2153250619 @default.
- W3187378970 cites W2157466346 @default.
- W3187378970 cites W2174633205 @default.
- W3187378970 cites W2206368938 @default.
- W3187378970 cites W2224137722 @default.
- W3187378970 cites W2292221433 @default.
- W3187378970 cites W2322271209 @default.
- W3187378970 cites W2329888282 @default.
- W3187378970 cites W2475148876 @default.
- W3187378970 cites W2520630506 @default.
- W3187378970 cites W2539777782 @default.
- W3187378970 cites W2545703737 @default.
- W3187378970 cites W2550254595 @default.
- W3187378970 cites W2586702633 @default.
- W3187378970 cites W2593588874 @default.
- W3187378970 cites W2624346565 @default.
- W3187378970 cites W2734832333 @default.
- W3187378970 cites W2745417329 @default.
- W3187378970 cites W2757271110 @default.
- W3187378970 cites W2767155882 @default.
- W3187378970 cites W2775788879 @default.
- W3187378970 cites W2795064020 @default.
- W3187378970 cites W2796356626 @default.
- W3187378970 cites W2797024694 @default.
- W3187378970 cites W2802211415 @default.
- W3187378970 cites W2803090911 @default.
- W3187378970 cites W2804675995 @default.
- W3187378970 cites W2889646458 @default.
- W3187378970 cites W2913716396 @default.
- W3187378970 cites W2914151360 @default.
- W3187378970 cites W2931549096 @default.
- W3187378970 cites W2933273868 @default.
- W3187378970 cites W2942607964 @default.
- W3187378970 cites W2947060096 @default.
- W3187378970 cites W2968505986 @default.
- W3187378970 cites W2977451996 @default.
- W3187378970 cites W2997492439 @default.
- W3187378970 cites W3021690689 @default.
- W3187378970 cites W3095068451 @default.