He Ningning, Feng Guowei, Li Yang, Xu Yang, Xie Xiaoyan, Wang Hui, Wang Yuebing, Ou Lailiang, Pei Xuetao, Liu Na, Li Zongjin
School of Medicine, Nankai University, 94 Weijin Road, Tianjin, 300071, People's Republic of China.
Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, Nankai University, Tianjin, People's Republic of China.
Stem Cell Res Ther. 2016 Jul 27;7(1):95. doi: 10.1186/s13287-016-0360-x.
Microenvironment is being increasingly recognized as a critical determinant in tumor progression and metastasis. However, the appropriate regulatory mechanism to maintain the normal balance between differentiation and self-renewal of the cancer cell in microenvironment is not well known.
4T1 breast cancer cells were treated with embryonic stem (ES) cell conditioned medium which was collected from mouse ES cells. Inhibition of tumor cell growth was based on the reduction of cell proliferation and viability, and inhibition of aggressive properties of tumor cells were examined using the wound-healing and mammosphere assays. The expression of stem cell-associated genes was detected by quantitative RT-PCR.
We used a real-time imaging system to investigate the effect of the mouse ES cell microenvironment on aggressive breast cancer cells in vitro and in vivo. Exposure of breast cancer cells in mouse ES cell conditioned medium resulted in inhibition of growth, migration, metastasis, and angiogenesis of cancer cells. For many tumors, aggressive properties were tightly related to Stat3 signaling activation. We specifically discovered that the ES cell microenvironment sufficiently suppressed Stat3 signaling pathway activation in aggressive tumor cells, leading to a reduction in tumorigenesis and invasiveness.
We identified important functions of Stat3 and their implications for antitumor effects of ES cell conditioned medium. Some factors secreted by ES cells could efficiently suppress Stat3 pathway activation in breast cancer cells, and were then involved in cancer cell growth, survival, invasion, and migration. This study may act as a platform to understand tumor cell plasticity and may offer new therapeutic strategies to inhibit breast cancer progression.
微环境日益被认为是肿瘤进展和转移的关键决定因素。然而,维持微环境中癌细胞分化与自我更新之间正常平衡的适当调节机制尚不清楚。
用从小鼠胚胎干细胞收集的胚胎干细胞条件培养基处理4T1乳腺癌细胞。基于细胞增殖和活力的降低来抑制肿瘤细胞生长,并使用伤口愈合和乳腺球测定法检查肿瘤细胞侵袭性的抑制情况。通过定量逆转录聚合酶链反应检测干细胞相关基因的表达。
我们使用实时成像系统研究小鼠胚胎干细胞微环境对体外和体内侵袭性乳腺癌细胞的影响。将乳腺癌细胞暴露于小鼠胚胎干细胞条件培养基中会导致癌细胞生长、迁移、转移和血管生成受到抑制。对于许多肿瘤来说,侵袭性与信号转导和转录激活因子3(Stat3)信号激活密切相关。我们特别发现胚胎干细胞微环境充分抑制了侵袭性肿瘤细胞中Stat3信号通路的激活,从而导致肿瘤发生和侵袭性降低。
我们确定了Stat3的重要功能及其对胚胎干细胞条件培养基抗肿瘤作用的影响。胚胎干细胞分泌的一些因子可有效抑制乳腺癌细胞中Stat3通路的激活,并参与癌细胞生长、存活、侵袭和迁移。本研究可能成为理解肿瘤细胞可塑性的平台,并可能提供抑制乳腺癌进展的新治疗策略。