Tumor-penetrating therapy for β5 integrin-rich pancreas cancer

The iRGD tumor-penetrating peptide can achieve tumor specific drug delivery but whether and how it can penetrate into desmoplastic tumors is unknown. Here, the authors show that β5 integrin expression on tumor cells, mediated by CAFs-derived TGF-β, is required for iRGD penetration into the desmoplas...

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Autores principales: Tatiana Hurtado de Mendoza, Evangeline S. Mose, Gregory P. Botta, Gary B. Braun, Venkata R. Kotamraju, Randall P. French, Kodai Suzuki, Norio Miyamura, Tambet Teesalu, Erkki Ruoslahti, Andrew M. Lowy, Kazuki N. Sugahara
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Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/80f9f85745054067b544050e7b18b670
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spelling oai:doaj.org-article:80f9f85745054067b544050e7b18b6702021-12-02T13:34:55ZTumor-penetrating therapy for β5 integrin-rich pancreas cancer10.1038/s41467-021-21858-12041-1723https://doaj.org/article/80f9f85745054067b544050e7b18b6702021-03-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-21858-1https://doaj.org/toc/2041-1723The iRGD tumor-penetrating peptide can achieve tumor specific drug delivery but whether and how it can penetrate into desmoplastic tumors is unknown. Here, the authors show that β5 integrin expression on tumor cells, mediated by CAFs-derived TGF-β, is required for iRGD penetration into the desmoplastic PDAC microenvironment and that iRGD-based combination therapy is effective in PDAC mouse models.Tatiana Hurtado de MendozaEvangeline S. MoseGregory P. BottaGary B. BraunVenkata R. KotamrajuRandall P. FrenchKodai SuzukiNorio MiyamuraTambet TeesaluErkki RuoslahtiAndrew M. LowyKazuki N. SugaharaNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-13 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Tatiana Hurtado de Mendoza
Evangeline S. Mose
Gregory P. Botta
Gary B. Braun
Venkata R. Kotamraju
Randall P. French
Kodai Suzuki
Norio Miyamura
Tambet Teesalu
Erkki Ruoslahti
Andrew M. Lowy
Kazuki N. Sugahara
Tumor-penetrating therapy for β5 integrin-rich pancreas cancer
description The iRGD tumor-penetrating peptide can achieve tumor specific drug delivery but whether and how it can penetrate into desmoplastic tumors is unknown. Here, the authors show that β5 integrin expression on tumor cells, mediated by CAFs-derived TGF-β, is required for iRGD penetration into the desmoplastic PDAC microenvironment and that iRGD-based combination therapy is effective in PDAC mouse models.
format article
author Tatiana Hurtado de Mendoza
Evangeline S. Mose
Gregory P. Botta
Gary B. Braun
Venkata R. Kotamraju
Randall P. French
Kodai Suzuki
Norio Miyamura
Tambet Teesalu
Erkki Ruoslahti
Andrew M. Lowy
Kazuki N. Sugahara
author_facet Tatiana Hurtado de Mendoza
Evangeline S. Mose
Gregory P. Botta
Gary B. Braun
Venkata R. Kotamraju
Randall P. French
Kodai Suzuki
Norio Miyamura
Tambet Teesalu
Erkki Ruoslahti
Andrew M. Lowy
Kazuki N. Sugahara
author_sort Tatiana Hurtado de Mendoza
title Tumor-penetrating therapy for β5 integrin-rich pancreas cancer
title_short Tumor-penetrating therapy for β5 integrin-rich pancreas cancer
title_full Tumor-penetrating therapy for β5 integrin-rich pancreas cancer
title_fullStr Tumor-penetrating therapy for β5 integrin-rich pancreas cancer
title_full_unstemmed Tumor-penetrating therapy for β5 integrin-rich pancreas cancer
title_sort tumor-penetrating therapy for β5 integrin-rich pancreas cancer
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/80f9f85745054067b544050e7b18b670
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