Proteomic profiling reveals antitumor effects of RT2 peptide on a human colon carcinoma xenograft mouse model

A comparative study of human colon HCT-116 xenograft in nude mice treated with and without peptide RT2 at high doses is performed along with a label-free proteomic analysis of the tissue in order to understand the potential mechanisms by which RT2 acts in vivo against colorectal tumors. RT2 displays...

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Main Authors: Surachai Maijaroen, Sompong Klaynongsruang, Somrudee Reabroi, Arthit Chairoungdua, Sittiruk Roytrakul, Jureerut Daduang, Lapatrada Taemaitree, Nisachon Jangpromma
Other Authors: Khon Kaen University
Format: Article
Published: 2022
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/75250
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spelling th-mahidol.752502022-08-04T11:47:50Z Proteomic profiling reveals antitumor effects of RT2 peptide on a human colon carcinoma xenograft mouse model Surachai Maijaroen Sompong Klaynongsruang Somrudee Reabroi Arthit Chairoungdua Sittiruk Roytrakul Jureerut Daduang Lapatrada Taemaitree Nisachon Jangpromma Khon Kaen University Mahidol University Thailand National Center for Genetic Engineering and Biotechnology Pharmacology, Toxicology and Pharmaceutics A comparative study of human colon HCT-116 xenograft in nude mice treated with and without peptide RT2 at high doses is performed along with a label-free proteomic analysis of the tissue in order to understand the potential mechanisms by which RT2 acts in vivo against colorectal tumors. RT2 displays no significant systematic toxicity, but reduces tumor growth after either intraperitoneal or intratumoral injection demonstrating it is a safe and efficacious antitumor agent in vivo. Of the 3196 proteins identified by label-free proteomics, 61 proteins appear only in response to RT2 and are involved in cellular processes largely localized in the cells and cell parts. Some of the proteins identified, including CFTR, Wnt7a, TIA1, PADI2, NRBP2, GADL1, LZIC, TLR6, and GPR37, have been reported to suppress tumor growth and are associated with cell proliferation, invasion, metastasis, angiogenesis, apoptosis, and immune evasion. Our work supports their role as tumor biomarkers and reveals RT2 has a complex mechanism of action in vivo. 2022-08-04T04:47:50Z 2022-08-04T04:47:50Z 2022-02-15 Article European Journal of Pharmacology. Vol.917, (2022) 10.1016/j.ejphar.2022.174753 18790712 00142999 2-s2.0-85123117243 https://repository.li.mahidol.ac.th/handle/123456789/75250 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85123117243&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Pharmacology, Toxicology and Pharmaceutics
spellingShingle Pharmacology, Toxicology and Pharmaceutics
Surachai Maijaroen
Sompong Klaynongsruang
Somrudee Reabroi
Arthit Chairoungdua
Sittiruk Roytrakul
Jureerut Daduang
Lapatrada Taemaitree
Nisachon Jangpromma
Proteomic profiling reveals antitumor effects of RT2 peptide on a human colon carcinoma xenograft mouse model
description A comparative study of human colon HCT-116 xenograft in nude mice treated with and without peptide RT2 at high doses is performed along with a label-free proteomic analysis of the tissue in order to understand the potential mechanisms by which RT2 acts in vivo against colorectal tumors. RT2 displays no significant systematic toxicity, but reduces tumor growth after either intraperitoneal or intratumoral injection demonstrating it is a safe and efficacious antitumor agent in vivo. Of the 3196 proteins identified by label-free proteomics, 61 proteins appear only in response to RT2 and are involved in cellular processes largely localized in the cells and cell parts. Some of the proteins identified, including CFTR, Wnt7a, TIA1, PADI2, NRBP2, GADL1, LZIC, TLR6, and GPR37, have been reported to suppress tumor growth and are associated with cell proliferation, invasion, metastasis, angiogenesis, apoptosis, and immune evasion. Our work supports their role as tumor biomarkers and reveals RT2 has a complex mechanism of action in vivo.
author2 Khon Kaen University
author_facet Khon Kaen University
Surachai Maijaroen
Sompong Klaynongsruang
Somrudee Reabroi
Arthit Chairoungdua
Sittiruk Roytrakul
Jureerut Daduang
Lapatrada Taemaitree
Nisachon Jangpromma
format Article
author Surachai Maijaroen
Sompong Klaynongsruang
Somrudee Reabroi
Arthit Chairoungdua
Sittiruk Roytrakul
Jureerut Daduang
Lapatrada Taemaitree
Nisachon Jangpromma
author_sort Surachai Maijaroen
title Proteomic profiling reveals antitumor effects of RT2 peptide on a human colon carcinoma xenograft mouse model
title_short Proteomic profiling reveals antitumor effects of RT2 peptide on a human colon carcinoma xenograft mouse model
title_full Proteomic profiling reveals antitumor effects of RT2 peptide on a human colon carcinoma xenograft mouse model
title_fullStr Proteomic profiling reveals antitumor effects of RT2 peptide on a human colon carcinoma xenograft mouse model
title_full_unstemmed Proteomic profiling reveals antitumor effects of RT2 peptide on a human colon carcinoma xenograft mouse model
title_sort proteomic profiling reveals antitumor effects of rt2 peptide on a human colon carcinoma xenograft mouse model
publishDate 2022
url https://repository.li.mahidol.ac.th/handle/123456789/75250
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