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MOESM2 of Early detection of the major male cancer types in blood-based liquid biopsies using a DNA methylation panel

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posted on 2019-12-03, 04:42 authored by Vera Constâncio, Sandra Nunes, Catarina Moreira-Barbosa, Rui Freitas, Jorge Oliveira, Inês Pousa, Júlio Oliveira, Marta Soares, Carlos Dias, Teresa Dias, Luís Antunes, Rui Henrique, Carmen Jerónimo
Additional file 2: Figure S1. Distribution of methylation levels in PCa patients according with metastatic dissemination. (A) APC, (B) GSTP1, (C) HOXD3, (D) RARβ2, (E) RASSF1A and (F) SEPT9 promoter’s methylation levels between non-metastatic (M0) (n=116) and metastatic (M+) (n=5) PCa patients. Mann-Whitney U Test, ***p<0.001, ****p<0.0001. Red horizontal lines represent median methylation levels. Figure S2. Cumulative incidence function plots according to clinicopathological variables (A) regional node, (B) distant metastasis, (C) clinical stage and (D) histological subtype in LC patients. p-values obtained by Gray’s test for disease-specific mortality. Figure S3. Cumulative incidence function plots according to clinicopathological variables (A) ISUP Grade Group, (B) serum PSA levels, (C) clinical stage, and (D) APC, (E) GSTP1, (F) RARβ2, (G) RASSF1A, (H) SEPT9, (I) SOX17 promoter methylation levels in PCa patients. p-values obtained by Gray’s test for disease-specific mortality. Figure S4. Cumulative incidence function plots according to clinicopathological variable (A) distant metastasis, and (B) RARβ2, (C) SEPT9 and (D) SOX17 promoter methylation levels in CRC patients. p-values obtained by Gray’s test for disease-specific mortality.

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Research Center - Portuguese Oncology Institute of Porto

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