Department of Orthopedics , Renmin Hospital of Wuhan University , Wuhan 430060 , P. R. China.
Key Laboratory of Biomedical Polymers of Ministry of Education, Institute for Advanced Studies (IAS) and Department of Chemistry , Wuhan University , Wuhan 430072 , P. R. China.
ACS Nano. 2019 Aug 27;13(8):8618-8629. doi: 10.1021/acsnano.9b02993. Epub 2019 Jul 1.
Natural nanoparticles have been extensively studied due to their diverse properties and easy accessibility. Here, the nanoparticles extracted from cuttlefish ink (CINPs) with significant antitumor efficacy are explored. These CINPs, with spherical morphology, good dispersibility, and biocompatibility, are rich in melanin and contain a variety of amino acids and monosaccharides. Through the activation of mitogen-activated protein kinase (MAPK) signaling pathway, CINPs can efficiently reprogram tumor-associated macrophages (TAMs) from immune-suppressive M2-like phenotype to antitumor M1-like phenotype. Besides, under near-infrared (NIR) irradiation, CINPs exhibit high photothermal effect and tumor cell killing ability, which make them a potential candidate in photothermal therapy (PTT) of tumor. , CINPs can increase the proportion of M1 macrophages and foster the recruitment of cytotoxic T lymphocytes (CTLs) to tumors, leading to reduced primary tumor growth and lung metastasis. In combination with their photothermal effect, which can induce tumor-specific antigens release, CINPs could almost completely inhibit tumor growth accompanied by more active immune responses. Collectively, these CINPs described here can provide both tumor immunotherapy and PTT, implying that CINPs are promising for tumor treatment.
由于具有多样的性质和易于获取的特点,天然纳米颗粒得到了广泛的研究。在此,我们探索了具有显著抗肿瘤功效的墨鱼汁纳米颗粒(CINPs)。这些 CINPs 呈球形形态,具有良好的分散性和生物相容性,富含黑色素,并含有多种氨基酸和单糖。CINPs 通过激活丝裂原活化蛋白激酶(MAPK)信号通路,能够有效地将肿瘤相关巨噬细胞(TAMs)从免疫抑制的 M2 样表型重编程为抗肿瘤的 M1 样表型。此外,在近红外(NIR)照射下,CINPs 表现出高的光热效应和肿瘤细胞杀伤能力,使其成为肿瘤光热治疗(PTT)的潜在候选物。通过激活丝裂原活化蛋白激酶(MAPK)信号通路,CINPs 能够有效地将肿瘤相关巨噬细胞(TAMs)从免疫抑制的 M2 样表型重编程为抗肿瘤的 M1 样表型。此外,在近红外(NIR)照射下,CINPs 表现出高的光热效应和肿瘤细胞杀伤能力,使其成为肿瘤光热治疗(PTT)的潜在候选物。CINPs 可以增加 M1 巨噬细胞的比例,并促进细胞毒性 T 淋巴细胞(CTLs)向肿瘤的募集,从而导致原发肿瘤生长和肺转移的减少。结合其光热效应,可诱导肿瘤特异性抗原释放,CINPs 几乎可以完全抑制肿瘤生长,同时引发更活跃的免疫反应。总的来说,这里描述的 CINPs 既能提供肿瘤免疫治疗,又能提供光热治疗,这表明 CINPs 有望用于肿瘤治疗。