Lasso Paola, Gomez-Cadena Alejandra, Urueña Claudia, Donda Alena, Martinez-Usatorre Amaia, Barreto Alfonso, Romero Pedro, Fiorentino Susana
Grupo de Inmunobiología y Biología Celular, Pontificia Universidad Javeriana, Bogotá, Colombia.
Department of Oncology, Faculty of Biology and Medicine, University of Lausanne, Lausanne, Switzerland.
Front Oncol. 2018 Aug 30;8:356. doi: 10.3389/fonc.2018.00356. eCollection 2018.
Polyphenols have tumoricidal effects via anti-proliferative, anti-angiogenic and cytotoxic mechanisms and have recently been demonstrated to modulate the immune response through their anti- or pro- oxidant activity. Nevertheless, it remains controversial whether antioxidant-rich supplements have real beneficial effects on health, especially in complex diseases such as cancer. We previously identified a polyphenol-rich extract obtained from (P2Et) with anti-tumor activity in both breast carcinoma and melanoma. The present work evaluated the ability of P2Et extract to modulate the immune system in either the steady state or following tumor challenge. We found that the prophylactic treatment of healthy mice increased the number of CD4 and CD8 activated T, NK, regulatory T, dendritic and myeloid-derived suppressor cells in lymphoid organs together with a significant increase in plasma IL-6. Interestingly, this pre-conditioning of the host immune system with P2Et did not involve a protective effect against the control of tumor growth and metastasis in transplantable models of melanoma (B16) and breast cancer (4T1), but in contrast, a detrimental effect was observed in both models. We further demonstrated that this effect was at least partly due to an increase in regulatory T cells, myeloid-derived suppressor cells, and proinflammatory cytokines, with a concomitant decrease in CD4 and CD8 T cells. Taken together, these results suggest that the anti-tumor and immunomodulation properties of the P2Et extract critically depend on the presence of the tumor and might be mediated by the complex interactions between the tumor cells and the other components of the tumor microenvironment.
多酚类物质通过抗增殖、抗血管生成和细胞毒性机制发挥杀肿瘤作用,并且最近已证明其可通过抗氧化或促氧化活性调节免疫反应。然而,富含抗氧化剂的补充剂对健康是否具有真正的有益作用仍存在争议,尤其是在癌症等复杂疾病中。我们之前鉴定出一种从[具体来源未给出]获得的富含多酚的提取物(P2Et),其在乳腺癌和黑色素瘤中均具有抗肿瘤活性。目前的工作评估了P2Et提取物在稳态或肿瘤攻击后调节免疫系统的能力。我们发现,对健康小鼠进行预防性治疗可增加淋巴器官中CD4和CD8活化T细胞、自然杀伤细胞、调节性T细胞、树突状细胞和髓源性抑制细胞的数量,并使血浆白细胞介素-6显著增加。有趣的是,用P2Et对宿主免疫系统进行这种预处理在黑色素瘤(B16)和乳腺癌(4T1)的可移植模型中并未对肿瘤生长和转移的控制产生保护作用,相反,在这两种模型中均观察到有害作用。我们进一步证明,这种作用至少部分是由于调节性T细胞、髓源性抑制细胞和促炎细胞因子的增加,同时CD4和CD8 T细胞减少。综上所述,这些结果表明P2Et提取物的抗肿瘤和免疫调节特性严重依赖于肿瘤的存在,并且可能由肿瘤细胞与肿瘤微环境的其他成分之间的复杂相互作用介导。