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Tumor-targeting cell-penetrating peptide, p28, for glioblastoma imaging and therapy

Despite recent advances in cancer research, glioblastoma multiforme (GBM) remains a highly aggressive brain tumor as its treatment options are limited. The current standard treatment includes surgery followed by radiotherapy and adjuvant chemotherapy. However, surgery without image guidance is often...

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Autores principales: Mander, Sunam, Naffouje, Samer A., Gao, Jin, Li, Weiguo, Christov, Konstantin, Green, Albert, Bongarzone, Ernesto R., Das Gupta, Tapas K., Yamada, Tohru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353713/
https://www.ncbi.nlm.nih.gov/pubmed/35936749
http://dx.doi.org/10.3389/fonc.2022.940001
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author Mander, Sunam
Naffouje, Samer A.
Gao, Jin
Li, Weiguo
Christov, Konstantin
Green, Albert
Bongarzone, Ernesto R.
Das Gupta, Tapas K.
Yamada, Tohru
author_facet Mander, Sunam
Naffouje, Samer A.
Gao, Jin
Li, Weiguo
Christov, Konstantin
Green, Albert
Bongarzone, Ernesto R.
Das Gupta, Tapas K.
Yamada, Tohru
author_sort Mander, Sunam
collection PubMed
description Despite recent advances in cancer research, glioblastoma multiforme (GBM) remains a highly aggressive brain tumor as its treatment options are limited. The current standard treatment includes surgery followed by radiotherapy and adjuvant chemotherapy. However, surgery without image guidance is often challenging to achieve maximal safe resection as it is difficult to precisely discern the lesion to be removed from surrounding brain tissue. In addition, the efficacy of adjuvant chemotherapy is limited by poor penetration of therapeutics through the blood-brain barrier (BBB) into brain tissues, and the lack of tumor targeting. In this regard, we utilized a tumor-targeting cell-penetration peptide, p28, as a therapeutic agent to improve the efficacy of a current chemotherapeutic agent for GBM, and as a carrier for a fluorescence imaging agent for a clear identification of GBM. Here, we show that a near-infrared (NIR) imaging agent, ICG-p28 (a chemical conjugate of an FDA-approved NIR dye, indocyanine green ICG, and tumor-targeting p28 peptide) can preferentially localize tumors in multiple GBM animal models. Moreover, xenograft studies show that p28, as a therapeutic agent, can enhance the cytotoxic activity of temozolomide (TMZ), one of the few effective drugs for brain tumors. Collectively, our findings highlight the important role of the tumor-targeting peptide, which has great potential for intraoperative image-guided surgery and the development of new therapeutic strategies for GBM.
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spelling pubmed-93537132022-08-06 Tumor-targeting cell-penetrating peptide, p28, for glioblastoma imaging and therapy Mander, Sunam Naffouje, Samer A. Gao, Jin Li, Weiguo Christov, Konstantin Green, Albert Bongarzone, Ernesto R. Das Gupta, Tapas K. Yamada, Tohru Front Oncol Oncology Despite recent advances in cancer research, glioblastoma multiforme (GBM) remains a highly aggressive brain tumor as its treatment options are limited. The current standard treatment includes surgery followed by radiotherapy and adjuvant chemotherapy. However, surgery without image guidance is often challenging to achieve maximal safe resection as it is difficult to precisely discern the lesion to be removed from surrounding brain tissue. In addition, the efficacy of adjuvant chemotherapy is limited by poor penetration of therapeutics through the blood-brain barrier (BBB) into brain tissues, and the lack of tumor targeting. In this regard, we utilized a tumor-targeting cell-penetration peptide, p28, as a therapeutic agent to improve the efficacy of a current chemotherapeutic agent for GBM, and as a carrier for a fluorescence imaging agent for a clear identification of GBM. Here, we show that a near-infrared (NIR) imaging agent, ICG-p28 (a chemical conjugate of an FDA-approved NIR dye, indocyanine green ICG, and tumor-targeting p28 peptide) can preferentially localize tumors in multiple GBM animal models. Moreover, xenograft studies show that p28, as a therapeutic agent, can enhance the cytotoxic activity of temozolomide (TMZ), one of the few effective drugs for brain tumors. Collectively, our findings highlight the important role of the tumor-targeting peptide, which has great potential for intraoperative image-guided surgery and the development of new therapeutic strategies for GBM. Frontiers Media S.A. 2022-07-22 /pmc/articles/PMC9353713/ /pubmed/35936749 http://dx.doi.org/10.3389/fonc.2022.940001 Text en Copyright © 2022 Mander, Naffouje, Gao, Li, Christov, Green, Bongarzone, Das Gupta and Yamada https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Mander, Sunam
Naffouje, Samer A.
Gao, Jin
Li, Weiguo
Christov, Konstantin
Green, Albert
Bongarzone, Ernesto R.
Das Gupta, Tapas K.
Yamada, Tohru
Tumor-targeting cell-penetrating peptide, p28, for glioblastoma imaging and therapy
title Tumor-targeting cell-penetrating peptide, p28, for glioblastoma imaging and therapy
title_full Tumor-targeting cell-penetrating peptide, p28, for glioblastoma imaging and therapy
title_fullStr Tumor-targeting cell-penetrating peptide, p28, for glioblastoma imaging and therapy
title_full_unstemmed Tumor-targeting cell-penetrating peptide, p28, for glioblastoma imaging and therapy
title_short Tumor-targeting cell-penetrating peptide, p28, for glioblastoma imaging and therapy
title_sort tumor-targeting cell-penetrating peptide, p28, for glioblastoma imaging and therapy
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353713/
https://www.ncbi.nlm.nih.gov/pubmed/35936749
http://dx.doi.org/10.3389/fonc.2022.940001
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