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Bcl-2 和 Fas 的表达与乳腺癌中脂肪来源干细胞 (ASCs) 的增殖特异性相关。

Bcl-2 and Fas expressions correlate with proliferative specificity of adipose-derived stem cells (ASCs) in breast cancer.

机构信息

Shiraz Institute for Cancer Research, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Immunol Invest. 2011;40(3):290-8. doi: 10.3109/08820139.2010.540892. Epub 2011 Jan 4.

Abstract

The tumor microenvironment consists of a dynamic interaction with several cell types including infiltrating cells from the immune system, fibroblasts, adipose derived stem cells (ASCs), and an appropriate milieu for tumor cell growth, expansion and spreading. The aim of this study was to focus on ASCs function by isolating and characterizing them from both breast cancer and normal breast adipose tissues. Therefore, the expressions of Bcl-2 and Fas mRNAs in these cells were determined using real-time quantitative PCR (Q-PCR). Also the proliferative properties of ASCs were compared among different pathological states and normal ASCs utilizing the MTT assay. It was observed that, Bcl-2 mRNA had 5-fold more expression in ASCs of patients than in controls. In contrast, Fas had a lower expression of mRNA in ASCs of patients compared to the controls. ASCs isolated from patients with stage 3 breast cancer had a statistically significant higher rate of proliferation compared to stage 2 and normal ASCs (P-value < 0.001). Based on these results, ASCs of the tumor microenvironment may contribute to tumor growth and progression and consequently protect tumor cells from the host immune response. Therefore these cells may be considered as therapeutic targets of cancer immunotherapy.

摘要

肿瘤微环境由多种细胞类型的动态相互作用组成,包括免疫系统浸润细胞、成纤维细胞、脂肪来源干细胞 (ASCs),以及有利于肿瘤细胞生长、扩增和扩散的环境。本研究的目的是专注于 ASC 的功能,从乳腺癌和正常乳腺脂肪组织中分离和鉴定它们。因此,使用实时定量 PCR (Q-PCR) 测定这些细胞中 Bcl-2 和 Fas mRNA 的表达。还利用 MTT 测定法比较了不同病理状态和正常 ASC 中 ASC 的增殖特性。结果表明,与对照组相比,患者 ASC 中的 Bcl-2 mRNA 表达增加了 5 倍。相比之下,Fas 在患者 ASC 中的 mRNA 表达较低。与 2 期和正常 ASC 相比,来自 3 期乳腺癌患者的 ASC 的增殖率具有统计学意义上的显著升高(P 值<0.001)。基于这些结果,肿瘤微环境中的 ASC 可能有助于肿瘤生长和进展,并因此保护肿瘤细胞免受宿主免疫反应的影响。因此,这些细胞可以被认为是癌症免疫治疗的治疗靶点。

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