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Unit polyion complex (uPIC) nanocarrier for siRNA delivery to glioblastoma and pancreatic cancer, Cancer Science

https://repo.qst.go.jp/records/85334
https://repo.qst.go.jp/records/85334
7871b9fa-0240-4ee9-bac7-aa55a10f87c5
Item type 会議発表論文 / Conference Paper(1)
公開日 2022-01-12
タイトル
タイトル Unit polyion complex (uPIC) nanocarrier for siRNA delivery to glioblastoma and pancreatic cancer, Cancer Science
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_5794
資源タイプ conference paper
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Watanabe, Sumiyo

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WEKO 1028515

Watanabe, Sumiyo

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Hayashi, Kotaro

× Hayashi, Kotaro

WEKO 1028516

Hayashi, Kotaro

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Tho, Kayoko

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WEKO 1028517

Tho, Kayoko

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Kim, Hunjin

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WEKO 1028518

Kim, Hunjin

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Chaya, Hiroyuki

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WEKO 1028519

Chaya, Hiroyuki

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Fukushima, Shigeto

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Fukushima, Shigeto

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Keisuke Katsushima

× Keisuke Katsushima

WEKO 1028521

Keisuke Katsushima

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Kondo, Yutaka

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WEKO 1028522

Kondo, Yutaka

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Ogura, Satomi

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WEKO 1028523

Ogura, Satomi

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Cabral, Horacio

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Cabral, Horacio

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Kensuke, Osada

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WEKO 1028525

Kensuke, Osada

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Nishiyama, Nobuhiro

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WEKO 1028526

Nishiyama, Nobuhiro

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Miyata, Kanjiro

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WEKO 1028527

Miyata, Kanjiro

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Kataoka, Kazunori

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Kataoka, Kazunori

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Kensuke, Osada

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内容記述タイプ Abstract
内容記述 There are critical issues in siRNA therapeutics, as follows, 1) siRNA is immediately degraded in extracellular milieu, such as bloodstream, 2)
the size of siRNA is -5nm, so siRNA is readily excreted from the kidney to the urine, and 3) the negative charge of siRNA repels the negatively
charged cell membrane, inhibiting the cellular uptake of siRNA. Thus, many previous studies have encapsulated siRNA into -100 nm-sized
nanoparticles to stabilize it. However, refractory cancers have tight barriers that prevent the penetration of such nanoparticles into cancer
cells. To overcome these hurdles, a new type of siRNA nanocarrier is developed for the cancer-targeted siRNA delivery, using a Y-shaped
block catiomer (YBC) with precisely regulated chain length and precisely neutralize their charges. Indeed, two YBCs are bound to a single
siRNA in the bloodstream, generating a dynamic polyin-pair, termed uPIC. Owing to both high stability in the bloodstream and ultra-small
(or optimal) size (-18 nm) to penetrate fibrotic tissues, uPIC efficiently delivers siRNA into murine models of fibrotic pancreatic cancer and
glioblastoma, exerting the significant anticancer activity in vivo.
書誌情報 Cancer Science

巻 112, p. 181, 発行日 2022-01
DOI
識別子タイプ DOI
関連識別子 10.1111/cas.14823
関連サイト
識別子タイプ URI
関連識別子 https://onlinelibrary.wiley.com/doi/10.1111/cas.14823
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