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B Fold Enrichment (Lep vs Mock) 0 2 4 6 8 Positive regulation of cell differentiation Negative regulation of epithelial-mesenchymal- transition Cell junction.

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Presentation on theme: "B Fold Enrichment (Lep vs Mock) 0 2 4 6 8 Positive regulation of cell differentiation Negative regulation of epithelial-mesenchymal- transition Cell junction."— Presentation transcript:

1 B Fold Enrichment (Lep vs Mock) 0 2 4 6 8 Positive regulation of cell differentiation Negative regulation of epithelial-mesenchymal- transition Cell junction organization Cell developmental process Cell morphogenesis ** Supplementary Figure S1 A Mock Leptin 47 253 STAT3 G9a 732 473 6111804 E miR-200c NUMB GATA3 FOXA2 miR-34a HOXA5 Leptin Mock ** * ** * Leptin+shSTAT3 * Leptin+shG9a MiR-200c 40 0 40 0 Mock Leptin 3kb 7072862 STAT3 G9a 3kb ch12: 7072862 H3K9Me2 30 0 C Supplementary Figure S1 Leptin induces STAT3-G9a interaction and their co- occupancy on targeted gene promoters. (A) Venn diagram showing overlap of STAT3 and G9a bound genes. (B) Gene ontology functional annotation of STAT3 and G 9a bound genes showing enrichment in specific biological processes. ChIP-seq results for (C) STAT3-G9a co- occupied MiR-200c with enhanced H3K9Me2 (bar positions denote the TSS) and (D) STAT3 and G9a peak distribution around TSS. (E) Fold change of miRNA/mRNA expression in MCF7 cells that expressed shSTAT3 or shG9a under leptin treatment (n=3, asterisk indicates P<0.05, double asterisk indicates P<0.01). Error bars denote ±SD. *

2 Leptin Mock Con-Vec miR-200c * B Con-Vec Leptin: - + miR-200c Con-Vec Leptin: - + Actin E-cad N-cad C D Leptin Mock Con-Vec miR-200c Con-Vec miR-200c * * MCF12AMCF7 E - + Leptin: miR-200c Con-Vec F Supplementary Figure 2 miR-200c-3p miR-124-3p miR-34a-5p miR-20b-5p Let-7f-5p miR-210-3p miR-21-5p miR-125a-5p ** Mock Leptin * * *** * * A Supplementary Figure S2 Leptin induces EMT and stem cell-like traits via down-regulation of miR-200c. (A) Genome-wide human miRNA array analysis showing miRNAs with significant expression changes in MCF12A cells treated with 50 ng/mL leptin for 12 hours (> 2 fold, n=3, asterisk indicates P<0.05, double asterisk indicates P<0.01). (B) Cell morphological change, (C) EMT protein expression (E-cadherin and N-cadherin), and (D) the percentage of CD24 - CD44 + population in MCF12A cells that stably expressed miR-200c and treated with 50 ng/mL leptin for 3 days (scale bar: 20  m, n=3, asterisk indicates P<0.05). (E) Representative images of spheres generated from MCF12A cells, and (F) the number of spheres generated from MCF12A and MCF7 cells that stably expressed miR-200c and treated with 50 ng/mL leptin for 7 days (scale bar: 100  m, n=3, asterisk indicates P<0.05). Error bars denote ±SD.

3 p-STAT3 STAT3 Actin OBR Leptin: - + sh-Vec sh-STAT3 - + G9a Actin OBR sh-Vec sh-G9a - + Leptin: - + AB Supplementary Figure S3 STAT3 and G9a expression is required for OBR induction by leptin. OBR protein expression levels in MCF7 cells that stably expressed (A) sh-STAT3 or (B) sh-G9a or the control sh-Vec under leptin treatment. Supplementary Figure S3

4 Supplementary Figure S4 Supplementary Figure S4 Distinct tumor phenotypes in Western obese animals compared to lean animals. (A) Animals in the highest tertile of body fat (determined by DEXA scan) were placed in the Western-obese group and those in the lowest tertile placed in the Western-lean group. Rats were then injected with 50 mg/kg MNU. Animals were palpated by 8 weeks after MNU injection and tumor incidences were monitored. (B) H&E staining showing aggressive adenocarcinoma (with tumor epithelial cells invading adjacent muscle tissue, black arrow) is the predominant tumor type in Western- obese animals, while Western-lean animals manifest benign adenoma (with low cuboidal epithelial cells forming duct-like structures, black arrow). Error bars denote ±SD. A B Obese Lean

5 Supplementary Figure S5 STAT3 activation and OBR overexpression in diet-induced obesity rats. (A) Representative leptin (LEP), p-STAT3, and OBR staining, and (B) fold change of miRNA/mRNA expression in mammary tissues of the obese and lean rats with Western diet, and the control rats with regular diet (scale bar=100um, n=5 animals/group, asterisk indicates P<0.05). (C, D) Immunoblots showing p-STAT3 levels in the tumor lysates collected on the indicated days (in between the days of treatment) from the MNU-treated obese rats with Western diet treated with S3I-201 or DMSO. (E) Quantification of p-STAT3 expression in (D) by ImageJ densitometry analysis (relative p-STAT3 level is normalized with total STAT3 and Actin, n=5 animals/group). Error bars denote ±SD. LEP OBR p-STAT3 Western-Obese Western-Lean Regular Chow A B miR-200c OBR Fold change of miRNA/mRNA expression * * Western-Lean Regular Chow Western-Obese - d3 d6 d9 d12 d3 d6 d9 d12 DMSOS3I-201 p-STAT3 STAT3 Actin d1 d4 d7 d10 d13 d3 d6 d9 d12 S3I-201or DMSO treatment Lysate collection C D E Relative expression of P-STAT3 Treatment: - d3 d6 d9 d12 d3 d6 d9 d12 DMSO P< 0.01 Supplementary Figure S5


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