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A Novel Topical Fluorescent Probe for Detection of Glioblastoma.
Kitagawa, Yosuke; Tanaka, Shota; Kamiya, Mako; Kuriki, Yugo; Yamamoto, Kyoko; Shimizu, Takenori; Nejo, Takahide; Hana, Taijun; Matsuura, Reiko; Koike, Tsukasa; Yamazawa, Erika; Kushihara, Yoshihiro; Takahashi, Satoshi; Nomura, Masashi; Takami, Hirokazu; Takayanagi, Shunsaku; Mukasa, Akitake; Urano, Yasuteru; Saito, Nobuhito.
Afiliação
  • Kitagawa Y; Department of Neurosurgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Tanaka S; Department of Neurosurgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan. stanaka@m.u-tokyo.ac.jp uranokun@m.u-tokyo.ac.jp.
  • Kamiya M; Laboratory of Chemical Biology and Molecular Imaging, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Kuriki Y; Laboratory of Chemistry and Biology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
  • Yamamoto K; Laboratory of Chemical Biology and Molecular Imaging, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Shimizu T; Department of Neurosurgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Nejo T; Department of Neurosurgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Hana T; Department of Neurosurgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Matsuura R; Department of Neurosurgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Koike T; Department of Neurosurgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Yamazawa E; Department of Neurosurgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Kushihara Y; Department of Neurosurgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Takahashi S; Department of Neurosurgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Nomura M; Department of Neurosurgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Takami H; Department of Neurosurgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Takayanagi S; Department of Neurosurgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Mukasa A; Department of Neurosurgery, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
  • Urano Y; Laboratory of Chemical Biology and Molecular Imaging, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan. stanaka@m.u-tokyo.ac.jp uranokun@m.u-tokyo.ac.jp.
  • Saito N; Laboratory of Chemistry and Biology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
Clin Cancer Res ; 27(14): 3936-3947, 2021 07 15.
Article em En | MEDLINE | ID: mdl-34031057
ABSTRACT

PURPOSE:

Five-aminolevulinic acid (5-ALA) is widely used as an intraoperative fluorescent probe for radical resection of high-grade glioma, and thus aids in extending progression-free survival of patients. However, there exist some cases where 5-ALA fails to fluoresce. In some other cases, it may undergo fluorescence quenching but cannot be orally readministered during surgery. This study aimed to develop a novel hydroxymethyl rhodamine green (HMRG)-based fluorescence labeling system that can be repeatedly administered as a topical spray during surgery for the detection of glioblastoma. EXPERIMENTAL

DESIGN:

We performed a three-stage probe screening using tumor lysates and fresh tumor tissues with our probe library consisting of a variety of HMRG probes with different dipeptides. We then performed proteome and transcript expression analyses to detect candidate enzymes responsible for cleaving the probe. Moreover, in vitro and ex vivo studies using U87 glioblastoma cell line were conducted to validate the findings.

RESULTS:

The probe screening identified proline-arginine-HMRG (PR-HMRG) as the optimal probe that distinguished tumors from peritumoral tissues. Proteome analysis identified calpain-1 (CAPN1) to be responsible for cleaving the probe. CAPN1 was highly expressed in tumor tissues which reacted to the PR-HMRG probe. Knockdown of this enzyme suppressed fluorescence intensity in U87 glioblastoma cells. In situ assay using a mouse U87 xenograft model demonstrated marked contrast of fluorescence with the probe between the tumor and peritumoral tissues.

CONCLUSIONS:

The novel fluorescent probe PR-HMRG is effective in detecting glioblastoma when applied topically. Further investigations are warranted to assess the efficacy and safety of its clinical use.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rodaminas / Neoplasias Encefálicas / Glioblastoma / Corantes Fluorescentes Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rodaminas / Neoplasias Encefálicas / Glioblastoma / Corantes Fluorescentes Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article