Translocator protein-targeted photodynamic therapy for direct and abscopal immunogenic cell death in colorectal cancer

被引:28
|
作者
Xie, Qing [1 ]
Li, Zhen [1 ,2 ]
Liu, Yang [1 ]
Zhang, Dawei [1 ,3 ]
Su, Meng [1 ]
Niitsu, Hiroaki [5 ]
Lu, Yuanyuan [5 ]
Coffey, Robert J. [4 ,5 ]
Bai, Mingfeng [1 ,6 ,7 ]
机构
[1] Vanderbilt Univ, Inst Imaging Sci, Med Ctr, 1161 21st Ave South, Nashville, TN 37232 USA
[2] China Med Univ, Dept Gen Surg, Affiliated Hosp 4, 4 Chongshan East Rd, Shenyang 110032, Peoples R China
[3] Guangzhou Med Univ, Dept Hepatobiliary Surg, Affiliated Hosp 2, 250 East Changgang Rd, Guangzhou 510260, Peoples R China
[4] Vanderbilt Univ, Dept Cell & Dev Biol, Sch Med, Nashville, TN 37232 USA
[5] Vanderbilt Univ, Dept Med, Med Ctr, Nashville, TN 37232 USA
[6] Vanderbilt Univ, Dept Radiol & Radiol Sci, Med Ctr, Nashville, TN 37232 USA
[7] Vanderbilt Univ, Vanderbilt Ingram Canc Ctr, Med Ctr, Nashville, TN 37232 USA
关键词
TSPO; Photodynamic therapy; Immunogenic cell death; Colorectal cancer; Anti-tumor immunity; PERIPHERAL BENZODIAZEPINE-RECEPTOR; ENDOPLASMIC-RETICULUM STRESS; CALRETICULIN EXPOSURE; BREAST-CANCER; EXPRESSION; PROLIFERATION; LOCALIZATION; MITOCHONDRIA; HYPERICIN; APOPTOSIS;
D O I
10.1016/j.actbio.2021.07.052
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Abscopal effect is an attractive cancer therapeutic effect referring to tumor regression at a location dis -tant from the primary treatment site. Immunogenic cell death (ICD) offers a mechanistic link between the primary and remote therapeutic effects by activating favorable anti-tumor immune responses. In this study, we induced ICD in colorectal cancer (CRC) cell lines in vitro and in vivo by targeting the 18 kDa translocator protein (TSPO), a mitochondrial receptor overexpressed in CRC. Photodynamic therapy (PDT) using a TSPO-targeted photosensitizer, IR700DX-6T, caused effective apoptotic cell death in fourteen CRC cell lines. In a syngeneic immunocompetent CRC mouse model, the growth of tumors subjected to TSPO-PDT was greatly suppressed. Remarkably, untreated tumors in the opposing flank also showed marked growth suppression. Dendritic and CD8(+) T cells were activated after TSPO-PDT treatment, accompanied by decreased Treg cells in both treated and non-treated tumors. In addition, a cancer vaccine developed from TSPO-PDT produced a significant tumor inhibition effect. These results indicate that TSPO-PDT could not only directly suppress tumor growth but also dramatically provoke host anti-tumor immunity, high-lighting the potential of TSPO-PDT as a successful therapeutic for CRC that exhibits systemic effects. Statement of significance Abscopal effect is an attractive cancer therapeutic effect referring to tumor regression at a location dis -tant from the primary treatment site. Immunogenic cell death (ICD) offers a mechanistic link between the primary and remote therapeutic effects by activating favorable anti-tumor immune responses. In this study, we report a new therapeutic approach that can reduce the growth of multiple CRC cell lines by in-ducing ICD. Notably, a direct and abscopal effect was observed in mouse tumor-derived MC38 cells when injected into syngeneic immunocompetent mice. If comparable effects could be achieved in humans, it would establish a novel paradigm for treating micro-and macro-metastasis. (c) 2021 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:716 / 729
页数:14
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