TY - JOUR
T1 - Photoimmunotherapy for cancer-associated fibroblasts targeting fibroblast activation protein in human esophageal squamous cell carcinoma
AU - Watanabe, Shinichiro
AU - Noma, Kazuhiro
AU - Ohara, Toshiaki
AU - Kashima, Hajime
AU - Sato, Hiroaki
AU - Kato, Takuya
AU - Urano, Shinichi
AU - Katsube, Ryoichi
AU - Hashimoto, Yuuri
AU - Tazawa, Hiroshi
AU - Kagawa, Shunsuke
AU - Shirakawa, Yasuhiro
AU - Kobayashi, Hisataka
AU - Fujiwara, Toshiyoshi
N1 - Funding Information:
This work was supported by Grants-in-Aid from the Ministry of Education, Science, and Culture, Japan; and Grants from the Ministry of Health and Welfare, Japan. H. Kobayashi was supported by the Intramural Research Program of the National Institutes of Health, National Cancer Institute, Center for Cancer Research. We would also like to thank Mr. Toru Tanida and Ms. Tae Yamanishi for their technical assistance and Drs. Oka and Miyazaki of Saiwaicho Hospital (Okayama, Japan) for useful discussions. We also thank Meenhard Herlyn for generously providing the FEF3 and GFP-FEF3 cell lines used in this study.
Funding Information:
CONTACT Kazuhiro Noma knoma@md.okayama-u.ac.jp Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama 700-8558, Japan Writing assistance This article has been edited by SPRINGER NATURE Author Services, funded by the grants listed. This article has been republished with minor changes. These changes do not impact the academic content of the article. Supplemental data for this article can be accessed on the publisher’s website. © 2019 Taylor & Francis Group, LLC
Publisher Copyright:
© 2019, © 2019 Taylor & Francis Group, LLC.
PY - 2019
Y1 - 2019
N2 - Cancer-associated fibroblasts (CAFs) are strongly implicated in tumor progression, including in the processes of tumorigenesis, invasion, and metastasis. The targeting of CAFs using various therapeutic approaches is a novel treatment strategy; however, the efficacy of such therapies remains limited. Recently, near-infrared photoimmunotherapy (NIR-PIT), which is a novel targeted therapy employing a cell-specific mAb conjugated to a photosensitizer, has been introduced as a new type of phototherapy. In this study, we have developed a novel NIR-PIT technique to target CAFs, by focusing on fibroblast activation protein (FAP), and we evaluate the treatment efficacy in vitro and in vivo. Esophageal carcinoma cells exhibited enhanced activation of fibroblasts, with FAP over-expressed in the cytoplasm and on the cell surface. FAP-IR700-mediated PIT showed induced rapid cell death specifically for those cells in vitro and in vivo, without adverse effects. This novel therapy for CAFs, designed as local control phototherapy, was safe and showed a promising inhibitory effect on FAP+ CAFs. PIT targeting CAFs via the specific marker FAP may be a therapeutic option for CAFs in the tumor microenvironment in the future.
AB - Cancer-associated fibroblasts (CAFs) are strongly implicated in tumor progression, including in the processes of tumorigenesis, invasion, and metastasis. The targeting of CAFs using various therapeutic approaches is a novel treatment strategy; however, the efficacy of such therapies remains limited. Recently, near-infrared photoimmunotherapy (NIR-PIT), which is a novel targeted therapy employing a cell-specific mAb conjugated to a photosensitizer, has been introduced as a new type of phototherapy. In this study, we have developed a novel NIR-PIT technique to target CAFs, by focusing on fibroblast activation protein (FAP), and we evaluate the treatment efficacy in vitro and in vivo. Esophageal carcinoma cells exhibited enhanced activation of fibroblasts, with FAP over-expressed in the cytoplasm and on the cell surface. FAP-IR700-mediated PIT showed induced rapid cell death specifically for those cells in vitro and in vivo, without adverse effects. This novel therapy for CAFs, designed as local control phototherapy, was safe and showed a promising inhibitory effect on FAP+ CAFs. PIT targeting CAFs via the specific marker FAP may be a therapeutic option for CAFs in the tumor microenvironment in the future.
KW - Tumor microenvironment
KW - esophageal cancer
KW - fibroblast activation protein (FAP)
KW - mouse model
KW - near-infrared photoimmunotherapy
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U2 - 10.1080/15384047.2019.1617566
DO - 10.1080/15384047.2019.1617566
M3 - Article
C2 - 31185791
AN - SCOPUS:85067577026
SN - 1538-4047
VL - 20
SP - 1234
EP - 1248
JO - Cancer Biology and Therapy
JF - Cancer Biology and Therapy
IS - 9
ER -