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Fig. 1 | Journal of Experimental & Clinical Cancer Research

Fig. 1

From: An immunotherapeutic approach to decipher the role of long non-coding RNAs in cancer progression, resistance and epigenetic regulation of immune cells

Fig. 1

LncRNA mediated molecular pathways in T Cells. In CTLs and Th cells, due to TCR signalling, there may be a Ca2+ influx, which can activate calmodulin. This promotes deacetylation of NILKA promoter, causing nuclear translocation of p300 inhibiting NF-kB pathway and activating AICD. In CD8+ cells, Lnc-NEAT1 regulates miR-155p mediated Tim-3 activation. While binding of Lnc-Tim-3 to Tim-3 protein inhibit Lck/NFAT1/AP-1 pathway and permit the localisation of Bat-3 towards p300 mediated activation of RelA and p53. In Th1 cells, EZH2 binds to LSD1, causing nuclear localization of EZH2, which inactivates transcription of MAF-4 gene by recruiting Linc-MAF-4 and H3K27 trimethylation of the promotor. In CD4+/CD8+ cells, Lnc-NeST and Lnc-HOTTIP binds to WDR5 protein of SET/MLL/WRD5 complex. The NeST can even recruit STAT to WDR5 through methylation. STAT4, thus gets localised to nucleus causing activation of IFN gamma pathways

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