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Therapeutic Effect of pHLIP-mediated CEACAM6 Gene Silencing in Lung Adenocarcinoma

Carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) plays an important role in lung cancer progression. Here, we examined the therapeutic efficacy of CEACAM6 gene silencing using an siRNA delivery platform targeting the acidic tumour microenvironment in a lung adenocarcinoma xenograf...

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Autores principales: Son, Seung-Myoung, Yun, Jieun, Lee, Sung-Hoon, Han, Hye Sook, Lim, Young Hyun, Woo, Chang Gok, Lee, Ho-Chang, Song, Hyung Geun, Gu, Young-Mi, Lee, Hyun-Jun, Lee, Ok-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717735/
https://www.ncbi.nlm.nih.gov/pubmed/31474761
http://dx.doi.org/10.1038/s41598-019-48104-5
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author Son, Seung-Myoung
Yun, Jieun
Lee, Sung-Hoon
Han, Hye Sook
Lim, Young Hyun
Woo, Chang Gok
Lee, Ho-Chang
Song, Hyung Geun
Gu, Young-Mi
Lee, Hyun-Jun
Lee, Ok-Jun
author_facet Son, Seung-Myoung
Yun, Jieun
Lee, Sung-Hoon
Han, Hye Sook
Lim, Young Hyun
Woo, Chang Gok
Lee, Ho-Chang
Song, Hyung Geun
Gu, Young-Mi
Lee, Hyun-Jun
Lee, Ok-Jun
author_sort Son, Seung-Myoung
collection PubMed
description Carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) plays an important role in lung cancer progression. Here, we examined the therapeutic efficacy of CEACAM6 gene silencing using an siRNA delivery platform targeting the acidic tumour microenvironment in a lung adenocarcinoma xenograft mouse model. An siRNA delivery vector was constructed by tethering the peptide nucleic acid form of an siRNA targeting CEACAM6 (siCEACAM6) to a peptide with a low pH-induced transmembrane structure (pHLIP) to transport siRNAs across the plasma membrane. Specific binding of the pHLIP-siCEACAM6 conjugate to A549 lung adenocarcinoma cells at low pH was demonstrated by flow cytometry. A549 cells incubated with pHLIP-siCEACAM6 at an acidic pH showed downregulated expression of endogenous CEACAM6 protein and reduced cell viability. The in vivo tumour-suppressing effects of pHLIP-siCEACAM6 in lung adenocarcinoma were assessed in a xenograft model generated by injecting BALB/c nude mice with A549 cells. pHLIP-siCEACAM6 treatment alone resulted in tumour growth inhibition of up to 35.5%. When combined with cisplatin treatment, pHLIP-siCEACAM6 markedly enhanced tumour growth inhibition by up to 47%. In conclusion, the delivery of siCEACAM6 to lung adenocarcinoma using the pHLIP peptide has therapeutic potential as a unique cancer treatment approach.
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spelling pubmed-67177352019-09-17 Therapeutic Effect of pHLIP-mediated CEACAM6 Gene Silencing in Lung Adenocarcinoma Son, Seung-Myoung Yun, Jieun Lee, Sung-Hoon Han, Hye Sook Lim, Young Hyun Woo, Chang Gok Lee, Ho-Chang Song, Hyung Geun Gu, Young-Mi Lee, Hyun-Jun Lee, Ok-Jun Sci Rep Article Carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) plays an important role in lung cancer progression. Here, we examined the therapeutic efficacy of CEACAM6 gene silencing using an siRNA delivery platform targeting the acidic tumour microenvironment in a lung adenocarcinoma xenograft mouse model. An siRNA delivery vector was constructed by tethering the peptide nucleic acid form of an siRNA targeting CEACAM6 (siCEACAM6) to a peptide with a low pH-induced transmembrane structure (pHLIP) to transport siRNAs across the plasma membrane. Specific binding of the pHLIP-siCEACAM6 conjugate to A549 lung adenocarcinoma cells at low pH was demonstrated by flow cytometry. A549 cells incubated with pHLIP-siCEACAM6 at an acidic pH showed downregulated expression of endogenous CEACAM6 protein and reduced cell viability. The in vivo tumour-suppressing effects of pHLIP-siCEACAM6 in lung adenocarcinoma were assessed in a xenograft model generated by injecting BALB/c nude mice with A549 cells. pHLIP-siCEACAM6 treatment alone resulted in tumour growth inhibition of up to 35.5%. When combined with cisplatin treatment, pHLIP-siCEACAM6 markedly enhanced tumour growth inhibition by up to 47%. In conclusion, the delivery of siCEACAM6 to lung adenocarcinoma using the pHLIP peptide has therapeutic potential as a unique cancer treatment approach. Nature Publishing Group UK 2019-09-02 /pmc/articles/PMC6717735/ /pubmed/31474761 http://dx.doi.org/10.1038/s41598-019-48104-5 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Son, Seung-Myoung
Yun, Jieun
Lee, Sung-Hoon
Han, Hye Sook
Lim, Young Hyun
Woo, Chang Gok
Lee, Ho-Chang
Song, Hyung Geun
Gu, Young-Mi
Lee, Hyun-Jun
Lee, Ok-Jun
Therapeutic Effect of pHLIP-mediated CEACAM6 Gene Silencing in Lung Adenocarcinoma
title Therapeutic Effect of pHLIP-mediated CEACAM6 Gene Silencing in Lung Adenocarcinoma
title_full Therapeutic Effect of pHLIP-mediated CEACAM6 Gene Silencing in Lung Adenocarcinoma
title_fullStr Therapeutic Effect of pHLIP-mediated CEACAM6 Gene Silencing in Lung Adenocarcinoma
title_full_unstemmed Therapeutic Effect of pHLIP-mediated CEACAM6 Gene Silencing in Lung Adenocarcinoma
title_short Therapeutic Effect of pHLIP-mediated CEACAM6 Gene Silencing in Lung Adenocarcinoma
title_sort therapeutic effect of phlip-mediated ceacam6 gene silencing in lung adenocarcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717735/
https://www.ncbi.nlm.nih.gov/pubmed/31474761
http://dx.doi.org/10.1038/s41598-019-48104-5
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