138 research outputs found

    Supplementary Figure 1 from TFF2–CXCR4 Axis Is Associated with <i>BRAF</i> V600E Colon Cancer

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    Supplementary Figure 1. Normalized TFF2 mRNA expression vs. phospho-ERK1/2 protein levels in BRAF WT tumors.</p

    Supplementary Table 1 from TFF2–CXCR4 Axis Is Associated with <i>BRAF</i> V600E Colon Cancer

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    Supplementary Table 1. Natural language processing results to identify senescence suppressors that are two-fold overexpressed in sessile serrated polyps.</p

    Distribution of MSI-L/MSS colorectal cancers according to the number of methylated promoters

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    <p><b>Copyright information:</b></p><p>Taken from "18q loss of heterozygosity in microsatellite stable colorectal cancer is correlated with CpG island methylator phenotype-negative (CIMP-0) and inversely with CIMP-low and CIMP-high"</p><p>http://www.biomedcentral.com/1471-2407/7/72</p><p>BMC Cancer 2007;7():72-72.</p><p>Published online 2 May 2007</p><p>PMCID:PMC1876238.</p><p></p> The X and Y axes indicate the number of methylated promoters and the number of tumors, respectively. Based on the and mutation rates, CIMP-high is defined as the presence of ≥ 6/8 methylated promoters. Also note that CIMP-0 tumors with 0/8 methylated promoters are more likely to have both wild-type and , compared to CIMP-low tumors with 1/8 to 5/8 methylated promoters. Abbreviations: BRAF+, -mutated wild-type; KRAS+, -mutated wild-type; K+/B+, -mutated -mutated; KRAS/BRAF WT, both wild-type and ; MSI-L, microsatellite instability-low; MSS, microsatellite stable

    Baseline characteristics of the Nurses' Health Study cohort<sup>*</sup>.

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    <p>*Dietary intake and other characteristics at baseline questionnaire in 1980 (mean value, unless otherwise indicated).</p>Ψ<p>All values have been directly standardized according to the age distribution of the cohort.</p>†<p>Pack-years were calculated for former and current smokers only.</p>‡<p>The body-mass index is the weight in kilograms divided by the square of the height in meters.</p>§<p>METS are metabolic equivalents. This was calculated based on the frequency of physical activities (such as jogging) in 1986.</p

    Risk of colon cancer according to baseline quintiles of one-carbon nutrient intake by BRAF mutation status in tumors among 88,691 women in the Nurses' Health Study (1980–2002).

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    ‡<p>Age adjusted only.</p><p>*All models are adjusted for age (continuous), energy intake, gender, screening sigmoidoscopy, family history of colorectal cancer, aspirin use, smoking, physical activity in METs, baseline body mass index, a history of colon polyps, beef intake, calcium, multi-vitamin use, and baseline folate, vitamin B<sub>6</sub>, B<sub>12</sub>, methionine, and alcohol if not primary exposure.</p

    Frequency of 18q LOH in MSI-L/MSS colorectal cancers, according to the number of methylated promoters

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    <p><b>Copyright information:</b></p><p>Taken from "18q loss of heterozygosity in microsatellite stable colorectal cancer is correlated with CpG island methylator phenotype-negative (CIMP-0) and inversely with CIMP-low and CIMP-high"</p><p>http://www.biomedcentral.com/1471-2407/7/72</p><p>BMC Cancer 2007;7():72-72.</p><p>Published online 2 May 2007</p><p>PMCID:PMC1876238.</p><p></p> CIMP-0 tumors (N = 200) with 0 methylated promoters show the highest frequency of 18q LOH

    Risk of colon cancer according to baseline quintiles of one-carbon nutrient intake by CIMP expression in tumors among 88,691 women in the Nurses' Health Study (1980–2002).

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    ‡<p>Age adjusted only.</p><p>*All models are adjusted for age (continuous), energy intake, gender, screening sigmoidoscopy, family history of colorectal cancer, aspirin use, smoking, physical activity in METs, baseline body mass index, a history of colon polyps, beef intake, calcium, multi-vitamin use, and baseline folate, vitamin B6, B12, methionine, and alcohol if not primary exposure. P for heterogeneity of the association for folate intake and CIMP-low/0 colon cancer versus folate intake and CIMP-high colon cancers = 0.73 (χ<sup>2</sup> = 1.31, 3 d.f.).</p><p>P for heterogeneity of the association for vitamin B<sub>6</sub> intake and CIMP-high colon cancer and vitamin B<sub>6</sub> intake and CIMP-low/0 colon cancers = 0.63 (χ<sup>2</sup> = 2.6, 4 d.f.) and for vitamin B<sub>12</sub> intake = 0.94 (χ<sup>2</sup> = 0.79, 4 d.f.). P for heterogeneity of the association for methionine intake and CIMP-high colon cancer and methionine intake and CIMP-low/0 colon cancers = 0.007 (χ<sup>2</sup> = 14.097, 4 d.f.), and for alcohol intake = 0.32 (χ<sup>2</sup> = 3.52, 3 d.f.).</p

    Supplementary Methods and tables from Plasma Inflammatory Markers and Risk of Advanced Colorectal Adenoma in Women

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    This file contains supplementary methods on assessment of dietary and lifestyle factors, and supplementary table 1 (Stratified association of plasma MIC-1 level with risk of advanced colorectal adenomas in the Nurses' Health Study (1990-2008)).</p
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