Basu Samar, Combe Kristell, Kwiatkowski Fabrice, Caldefie-Chézet Florence, Penault-Llorca Frédérique, Bignon Yves-Jean, Vasson Marie-Paule
Clermont Université, Université d'Auvergne, UMR 1019, Unité de Nutrition Humaine, CRNH-Auvergne, BP 10448, F-63000, Clermont-Ferrand, France; Oxidative Stress and Inflammation, Department of Public Health and Caring Sciences, Faculty of Medicine, Uppsala University, Uppsala, Sweden.
Clermont Université, Université d'Auvergne, UMR 1019, Unité de Nutrition Humaine, CRNH-Auvergne, BP 10448, F-63000, Clermont-Ferrand, France.
PLoS One. 2015 Oct 2;10(10):e0138443. doi: 10.1371/journal.pone.0138443. eCollection 2015.
Current evidences suggest that expression of Ki67, cyclooxygenase (COX), aromatase, adipokines, prostaglandins, free radicals, β-catenin and α-SMA might be involved in breast cancer pathogenesis. The main objective of this study was to compare expression/localization of these potential compounds in breast cancer tissues with tissues collected adjacent to the tumor using immunohistochemistry and correlated with clinical pathology. The breast cancer specimens were collected from 30 women aged between 49 and 89 years who underwent breast surgery following cancer diagnosis. Expression levels of molecules by different stainings were graded as a score on a scale based upon staining intensity and proportion of positive cells/area or individually. AdipoR1, adiponectin, Ob-R, leptin, COX-1, COX-2, aromatase, PGF2α, F2-isoprostanes and α-SMA were localised on higher levels in the breast tissues adjacent to the tumor compared to tumor specimens when considering either score or staining area whereas COX-2 and AdipoR2 were found to be higher considering staining intensity and Ki67 on score level in the tumor tissue. There was no significant difference observed on β-catenin either on score nor on staining area and intensity between tissues adjacent to the tumor and tumor tissues. A positive correlation was found between COX-1 and COX-2 in the tumor tissues. In conclusion, these suggest that Ki67, COXs, aromatase, prostaglandin, free radicals, adipokines, β-catenin and α-SMA are involved in breast cancer. These further focus the need of examination of tissues adjacent to tumor, tumor itself and compare them with normal or benign breast tissues for a better understanding of breast cancer pathology and future evaluation of therapeutic benefit.
目前的证据表明,Ki67、环氧化酶(COX)、芳香化酶、脂肪因子、前列腺素、自由基、β-连环蛋白和α-平滑肌肌动蛋白的表达可能与乳腺癌的发病机制有关。本研究的主要目的是通过免疫组织化学比较这些潜在化合物在乳腺癌组织与肿瘤旁组织中的表达/定位,并与临床病理相关联。乳腺癌标本取自30名年龄在49至89岁之间的女性,她们在癌症诊断后接受了乳房手术。不同染色的分子表达水平根据染色强度和阳性细胞比例/面积进行评分分级,或单独分级。当考虑评分或染色面积时,与肿瘤标本相比,脂联素受体1、脂联素、瘦素受体、瘦素、COX-1、COX-2、芳香化酶、前列腺素F2α、F2-异前列腺素和α-平滑肌肌动蛋白在肿瘤旁乳腺组织中的定位水平更高,而在肿瘤组织中,考虑染色强度时COX-2和脂联素受体2更高,考虑评分水平时Ki67更高。在肿瘤旁组织和肿瘤组织之间,β-连环蛋白在评分、染色面积和强度方面均未观察到显著差异。在肿瘤组织中发现COX-1和COX-2之间存在正相关。总之,这些表明Ki67、COXs、芳香化酶、前列腺素、自由基、脂肪因子、β-连环蛋白和α-平滑肌肌动蛋白与乳腺癌有关。这些进一步突出了检查肿瘤旁组织、肿瘤本身并将它们与正常或良性乳腺组织进行比较的必要性,以便更好地理解乳腺癌病理学和未来治疗益处的评估。