Dietary protein sources and tumoral overexpression of RhoA, VEGF-A and VEGFR2 genes among breast cancer patients.

IF 3.3 3区 医学 Q2 GENETICS & HEREDITY
Genes and Nutrition Pub Date : 2019-07-09 eCollection Date: 2019-01-01 DOI:10.1186/s12263-019-0645-7
Ali Shokri, Saeed Pirouzpanah, Mitra Foroutan-Ghaznavi, Vahid Montazeri, Ashraf Fakhrjou, Hojjatollah Nozad-Charoudeh, Gholamreza Tavoosidana
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引用次数: 0

Abstract

Background: High protein intake may promote angiogenesis giving support to the development of metastasis according to the experimental data. However, nutritional epidemiologic evidence is inconsistent with metastasis. Therefore, we aimed to study the association between dietary intake of protein and tumoral expression levels of Ras homologous gene family member A (RhoA), vascular endothelial growth factor-A (VEGF-A), and VEGF receptor-2 (VEGFR2) in primary breast cancer (BC) patients.

Methods: Over this consecutive case series, 177 women primary diagnosed with histopathologically confirmed BC in Tabriz (Iran) were enrolled between May 2011 and November 2016. A validated food frequency questionnaire was completed for eligible participants. Fold change in gene expression was measured using quantitative real-time PCR. Principal component factor analysis (PCA) was used to express dietary groups of proteins.

Results: Total protein intake was associated with the expression level of VEGF-A in progesterone receptor-positive (PR+: β = 0.296, p < 0.01) and VEGFR2 in patients with involvement of axillary lymph node metastasis (ALNM+: β = 0.295, p < 0.01) when covariates were adjusted. High animal protein intake was correlated with overexpression of RhoA in tumors with estrogen receptor-positive (ER+: β = 0.230, p < 0.05), ALNM+ (β = 0.238, p < 0.05), and vascular invasion (VI+: β = 0.313, p < 0.01). Animal protein intake was correlated with the overexpression of VEGFR2 when tumors were positive for hormonal receptors (ER+: β = 0.299, p < 0.01; PR+: β = 0.296, p < 0.01). Based on the PCA outputs, protein provided by whole meat (white and red meat) was associated inversely with RhoA expression in ALNM+ (β = - 0.253, p < 0.05) and premenopausal women (β = - 0.285, p < 0.01) in adjusted models. Whole meat was correlated with VEGFR2 overexpression in VI+ (β = 0.288, p < 0.05) and premenopausal status (β = 0.300, p < 0.05) in adjusted models. A group composed of dairy products and legumes was correlated with the overexpression of RhoA (β = 0.249, p < 0.05) and VEGF-A (β = 0.297, p < 0.05) in VI+.

Conclusions: Based on the multivariate findings, the dietary protein could associate with the overexpression of RhoA and VEGF-VEGFR2 in favor of lymphatic and vascular metastasis in BC patients.

Abstract Image

癌症患者的饮食蛋白质来源和RhoA、VEGF-A和VEGFR2基因的肿瘤过度表达。
背景:根据实验数据,高蛋白摄入可能促进血管生成,支持转移的发展。然而,营养流行病学证据与转移不一致。因此,我们旨在研究癌症(BC)患者膳食蛋白质摄入量与Ras同源基因家族成员A(RhoA)、血管内皮生长因子-A(VEGF-A)和VEGF受体-2(VEGFR2)肿瘤表达水平之间的关系。方法:在这一连续的病例系列中,2011年5月至2016年11月,在大不里士(伊朗),177名经组织病理学确诊为BC的女性被纳入研究。为符合条件的参与者完成了一份经过验证的食物频率问卷。使用定量实时PCR测量基因表达的倍数变化。主成分因子分析(PCA)用于表达膳食中的蛋白质组。结果:调整协变量后,总蛋白摄入量与参与腋窝淋巴结转移的患者中孕激素受体阳性的VEGF-A(PR+:β=0.296,p<0.01)和VEGFR2的表达水平相关(ALNM+:β=0.295,p<0.01)。在雌激素受体阳性(ER+:β=0.230,p<0.05)、ALNM+(β=0.238,p<0.05)的肿瘤中,高动物蛋白摄入与RhoA的过度表达相关,和血管侵袭(VI+:β=0.313,p<0.01)。当肿瘤激素受体呈阳性时,动物蛋白质摄入与VEGFR2的过度表达相关(ER+:β=0.0299,p<0.01;PR+:β-0.296,p<0.01),根据PCA输出,整肉(白肉和红肉)提供的蛋白质与ALNM+中RhoA的表达呈负相关(β=- 0.253,p<0.05)和绝经前妇女(β=- 0.285,p<0.01)。在调整模型中,整肉与VEGFR2在VI+中的过表达(β=0.288,p<0.05)和绝经前状态(β=0.300,p<0.05)相关。由乳制品和豆类组成的组与VI+中RhoA(β=0.249,p<0.05)和VEGF-A(β=0.0297,p<0.05)的过表达相关。结论:根据多变量研究结果,膳食蛋白质可能与RhoA和VEGF-VEGFR2的过表达有关,有利于BC患者的淋巴结和血管转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Genes and Nutrition
Genes and Nutrition 生物-遗传学
CiteScore
6.60
自引率
0.00%
发文量
14
审稿时长
6-12 weeks
期刊介绍: This journal examines the relationship between genetics and nutrition, with the ultimate goal of improving human health. It publishes original research articles and review articles on preclinical research data coming largely from animal, cell culture and other experimental models as well as critical evaluations of human experimental data to help deliver products with medically proven use.
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