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. 2021 Jun 18;17(5):677–691. doi: 10.1039/d1mo00117e

Fig. 5. Graphical summary. DNA methylation results reveal hypomethylation of SLFN11 promoter region in HCC1937 BRCA1 mutant cells. This combination has been shown to impact clinical treatment options. DNMT3A is a DNA methyltransferase and was elevated in HCC1937 cells along with Histone H3K36me. NSD2 is a histone methyltransferase elevated in MDA-MB-231 cells and is known to convert H3K36 to H3K36me1/2; transforming heterochromatin into euchromatin (active state). H3K36me2 recruits DNMT3A to shape the intergenic DNA methylation landscape. MDA-MB-231 cells showed increase TGFBR1, SMAD5 S465ph, and PTEN S385ph elevation leading to increased expression of TGFβ signaling and PI3K/AKT/mTOR pathways. HCC1937 cells had decreased expression of PTEN S385ph and decreased PI3K/AKT/mTOR and WNT/β-catenin pathways.

Fig. 5