Malfitano Anna Maria, Pisanti Simona, Napolitano Fabiana, Di Somma Sarah, Martinelli Rosanna, Portella Giuseppe
Department of Translational Medical Sciences, University of Naples Federico II, 80131 Naples, Italy.
Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Via Salvador Allende, Baronissi, 84081 Salerno, Italy.
Cancers (Basel). 2020 Jul 21;12(7):1987. doi: 10.3390/cancers12071987.
Tumor-associated macrophages (TAMs) represent the most abundant innate immune cells in tumors. TAMs, exhibiting anti-inflammatory phenotype, are key players in cancer progression, metastasis and resistance to therapy. A high TAM infiltration is generally associated with poor prognosis, but macrophages are highly plastic cells that can adopt either proinflammatory/antitumor or anti-inflammatory/protumor features in response to tumor microenvironment stimuli. In the context of cancer therapy, many anticancer therapeutics, apart from their direct effect on tumor cells, display different effects on TAM activation status and density. In this review, we aim to evaluate the indirect effects of anticancer therapies in the modulation of TAM phenotypes and pro/antitumor activity.
肿瘤相关巨噬细胞(TAM)是肿瘤中最丰富的固有免疫细胞。表现出抗炎表型的TAM是癌症进展、转移和治疗抵抗的关键参与者。TAM的高浸润通常与预后不良相关,但巨噬细胞是高度可塑性的细胞,可根据肿瘤微环境刺激呈现促炎/抗肿瘤或抗炎/促肿瘤特性。在癌症治疗背景下,许多抗癌疗法除了对肿瘤细胞有直接作用外,还对TAM的激活状态和密度表现出不同影响。在本综述中,我们旨在评估抗癌疗法在调节TAM表型和促/抗肿瘤活性方面的间接作用。