Cancer Biology Division, School of Biotechnology, Kalinga Institute of Industrial Technology (KIIT), Deemed to be University, Bhubaneswar-751024, Odisha, India.
School of Medical Science and Technology, Indian Institute of Technology Kharagpur-721302, West Bengal, India.
J Nutr Biochem. 2021 Jun;92:108624. doi: 10.1016/j.jnutbio.2021.108624. Epub 2021 Mar 8.
Tumor associated macrophages in the tumor microenvironment secrete multiple cytokines, which regulate cancer cells growth and invasiveness. We systematically studied the role of cytokines in the induction of cancer stem like cells (CSCs) in oral cancer cells niche and evaluated the mechanism of Resveratrol nanoparticle (Res-Nano) mediated-reduction of CSCs properties in cells. A highly M1-like macrophages-enriched conditioned medium (CM) was generated by treating fixed doses of PMA and LPS in THP-1 cells alone as well as co-cultured of H-357 plus THP-1 cells. These M1-like macrophages increased the production of cytokines (e.g., TNF-α, IL-6, IL-1β, etc.). A CSCs populated environment was created after addition of cytokine-enriched-CM of co-culture of H-357 and THP-1 cells to cancer cells and cytokine enriched CM of THP-1 cells to patient derived primary oral cancer cells, respectively. After incubation with CM, enhancement of stemness, angiogenic and metastatic properties of both H-357 and primary oral cancer cells were noted. Res-NP decreased the cytokines level in CSCs-enriched cells and reduced the invasion, proliferation and growth of CSCs. Representative metastatic (CD133, ALDH1, CXCR4, etc.) and angiogenic markers (MMPs, iNOS, VEGF-A, etc.) were decreased after Res-NP treatment in CSCs enriched oral cancer cells niche. It also disrupted angiogenesis, depleted nitric oxide production in fertilized chick embryos and reduced the expression of metastatic and angiogenic markers in xenograft mice model system. Thus, this study concluded that CSCs-mediated stemness is a cytokine dependent phenomena and treatment of Res-NP inhibit this process in in vitro, in vivo and ex vivo systems.
肿瘤相关巨噬细胞在肿瘤微环境中分泌多种细胞因子,调节癌细胞的生长和侵袭性。我们系统地研究了细胞因子在诱导口腔癌细胞龛中癌症干细胞样细胞(CSC)中的作用,并评估了白藜芦醇纳米粒子(Res-Nano)介导的CSC 特性降低的机制。通过单独用 PMA 和 LPS 处理固定剂量的 THP-1 细胞以及共培养 H-357 和 THP-1 细胞,生成了富含 M1 样巨噬细胞的条件培养基(CM)。这些 M1 样巨噬细胞增加了细胞因子(例如 TNF-α、IL-6、IL-1β 等)的产生。将共培养的 H-357 和 THP-1 细胞的富含细胞因子的 CM 添加到癌细胞中,或者将 THP-1 细胞的富含细胞因子的 CM 添加到患者来源的原发性口腔癌细胞中,分别创建了 CSC 种群环境。用 CM 孵育后,注意到 H-357 和原发性口腔癌细胞的干性、血管生成和转移特性增强。Res-NP 降低了 CSCs 富集细胞中的细胞因子水平,并减少了 CSCs 的侵袭、增殖和生长。Res-NP 处理 CSCs 富集的口腔癌细胞龛中的代表性转移性(CD133、ALDH1、CXCR4 等)和血管生成标志物(MMPs、iNOS、VEGF-A 等)减少。它还破坏了血管生成,耗尽了受精鸡胚中的一氧化氮产生,并减少了异种移植小鼠模型系统中的转移性和血管生成标志物的表达。因此,这项研究得出结论,CSC 介导的干性是一种细胞因子依赖的现象,Res-NP 的治疗抑制了体外、体内和体外系统中的这一过程。