Open Access
Open access
том 7 издание 1 номер публикации 579

sTRAIL-iRGD is a promising therapeutic agent for gastric cancer treatment

Ying Huang 1
Xihan Li 2
Huizi Sha 3
Lianru Zhang 3
XINYU BIAN 3
Xiao Han 4
Baorui Liu 3
Тип публикацииJournal Article
Дата публикации2017-04-03
scimago Q1
wos Q1
БС1
SJR0.874
CiteScore6.7
Impact factor3.9
ISSN20452322
Multidisciplinary
Краткое описание
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) selectively kills tumor cells and augments chemotherapeutics in vivo. Here, we developed sTRAIL-iRGD, a recombinant protein consisting of sTRAIL fused to CRGDKGPDC, a C-terminal end binding peptide with an integrin-binding arginine-glycine-aspartic acid (iRGD) motif. CRGDKGPDC is a tumor-homing peptide with high penetration into tumor tissue and cells. We found that sTRAIL-iRGD internalized into cultured gastric cancer tumor cells and localized to both the tumor mass in vivo and three-dimensional multicellular spheroids in vitro. sTRAIL-iRGD had an antitumor effect in tumor cell lines, multicellular spheroids and nude mice with tumors. Repeated treatment with sTRAIL-iRGD reduced tumor growth and volume in vivo. Mice treated with sTRAIL-iRGD and paclitaxel (PTX) in combination showed no sign of sTRAIL-iRGD-related liver toxicity. Our data suggest that sTRAIL-iRGD is a promising anti-gastric cancer agent with high selectivity and limited systemic toxicity.
Найдено 
Найдено 

Топ-30

Журналы

1
2
Drug Development Research
2 публикации, 11.76%
Antibodies
1 публикация, 5.88%
Cancers
1 публикация, 5.88%
Cells
1 публикация, 5.88%
International Journal of Molecular Sciences
1 публикация, 5.88%
Journal of Cancer Research and Clinical Oncology
1 публикация, 5.88%
Drug Delivery and Translational Research
1 публикация, 5.88%
Cell Death and Disease
1 публикация, 5.88%
International Journal of Pharmaceutics
1 публикация, 5.88%
Acta Biomaterialia
1 публикация, 5.88%
Biomaterials Science
1 публикация, 5.88%
Drug Delivery
1 публикация, 5.88%
Molecular Cancer Therapeutics
1 публикация, 5.88%
International Journal of Biological Macromolecules
1 публикация, 5.88%
Bulletin du Cancer
1 публикация, 5.88%
Russian Chemical Reviews
1 публикация, 5.88%
1
2

Издатели

1
2
3
4
MDPI
4 публикации, 23.53%
Elsevier
4 публикации, 23.53%
Springer Nature
3 публикации, 17.65%
Wiley
2 публикации, 11.76%
Royal Society of Chemistry (RSC)
1 публикация, 5.88%
Taylor & Francis
1 публикация, 5.88%
American Association for Cancer Research (AACR)
1 публикация, 5.88%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 публикация, 5.88%
1
2
3
4
  • Мы не учитываем публикации, у которых нет DOI.
  • Статистика публикаций обновляется еженедельно.

Вы ученый?

Создайте профиль, чтобы получать персональные рекомендации коллег, конференций и новых статей.
Метрики
17
Поделиться
Цитировать
ГОСТ |
Цитировать
Huang Y. et al. sTRAIL-iRGD is a promising therapeutic agent for gastric cancer treatment // Scientific Reports. 2017. Vol. 7. No. 1. 579
ГОСТ со всеми авторами (до 50) Скопировать
Huang Y., Li X., Sha H., Zhang L., BIAN X., Han X., Liu B. sTRAIL-iRGD is a promising therapeutic agent for gastric cancer treatment // Scientific Reports. 2017. Vol. 7. No. 1. 579
RIS |
Цитировать
TY - JOUR
DO - 10.1038/s41598-017-00688-6
UR - https://doi.org/10.1038/s41598-017-00688-6
TI - sTRAIL-iRGD is a promising therapeutic agent for gastric cancer treatment
T2 - Scientific Reports
AU - Huang, Ying
AU - Li, Xihan
AU - Sha, Huizi
AU - Zhang, Lianru
AU - BIAN, XINYU
AU - Han, Xiao
AU - Liu, Baorui
PY - 2017
DA - 2017/04/03
PB - Springer Nature
IS - 1
VL - 7
PMID - 28373646
SN - 2045-2322
ER -
BibTex
Цитировать
BibTex (до 50 авторов) Скопировать
@article{2017_Huang,
author = {Ying Huang and Xihan Li and Huizi Sha and Lianru Zhang and XINYU BIAN and Xiao Han and Baorui Liu},
title = {sTRAIL-iRGD is a promising therapeutic agent for gastric cancer treatment},
journal = {Scientific Reports},
year = {2017},
volume = {7},
publisher = {Springer Nature},
month = {apr},
url = {https://doi.org/10.1038/s41598-017-00688-6},
number = {1},
pages = {579},
doi = {10.1038/s41598-017-00688-6}
}