Reprogramming of CaCo2 colorectal cancer cells after using the complex of poly-(N-vinylpyrrolidone) with small non-coding RNAs

DOI: 10.1016/j.toxrep.2019.02.001

Keywords: SncRNAs, small non-coding RNAs, miR, micro-RNA, piR, piwi-interacting RNA, P-element induced wimpy testis interacting RNA, IL, interleukin, CD, cluster of differentiation, DTT, dithyothreitol, MKI-67, marker of proliferation ki-67, OCT4, octamer-binding transcription factor 4, mTOR, mechanistic target of rapamycin, VMAF, musculoaponeurotic fibrosarcoma, PIWIL1, piwi-like protein 1, BACH1, BTB domain and CNC homolog 1, HMOX1, heme oxygenase 1, RB1, retinoblastoma 1, DICER1, ribonuclease III, AGO2, argonaute 2, HOXA10, homebox A10, KIR1DL2, CD158b, expressed on natural killer cells and a subset of T cells, TGFBR2, transforming growth factor beta receptor 2, ICOS1B, inducible T-cell co-stimulator, GITR3A, glucocorticoid-induced TNFR-related protein, PNVP, poly-(N-vinylpyrrolidone), TNFRS6B, TNF receptor superfamily 6B, Wnt-1, wingless type MMTV integration site family, member 1, DNMT1, DNA methyltransferase 1, ERK1/2, extracellular signal regulated kinase ？, FGF2, fibroblast growth factor 2, iPS, induced pluripotent stem cells, H3K9me3, tri-methyl lysine 9 of histone H3, TSS, transcriptional start sites, HILI, human piwi, TE, transposon elements miRNA-152, piRNA-30074, Polymer carriers, CaCo2 colorectal adenocarcinoma, Reprogramming, Amphiphilic poly-(N-vinylpyrrolidone)

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