MiR-338-5p promotes metastasis of colorectal cancer by inhibition of phosphatidylinositol 3-kinase, catalytic subunit type 3-mediated autophagy pathwayResearch in context
Background: In our preliminary screening, expression of miR-338-5p was found to be higher in primary colorectal cancer (CRC) with metastasis. The autophagy related gene- phosphatidylinositol 3-kinase, catalytic subunit type 3 (PIK3C3) appeared to be targeted by miR-338-5p. Here, we provide solid evi...
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Format: | Article |
Language: | English |
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Elsevier
2019-05-01
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Series: | EBioMedicine |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2352396419302440 |
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doaj-d76130558dfb4fbbae0b98e63c873fb3 |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chien-An Chu Chung-Ta Lee Jenq-Chang Lee Yi-Wen Wang Ching-Tang Huang Sheng-Hui Lan Peng-Chan Lin Bo-Wen Lin Yu-Feng Tian Hsiao-Sheng Liu Nan-Haw Chow |
spellingShingle |
Chien-An Chu Chung-Ta Lee Jenq-Chang Lee Yi-Wen Wang Ching-Tang Huang Sheng-Hui Lan Peng-Chan Lin Bo-Wen Lin Yu-Feng Tian Hsiao-Sheng Liu Nan-Haw Chow MiR-338-5p promotes metastasis of colorectal cancer by inhibition of phosphatidylinositol 3-kinase, catalytic subunit type 3-mediated autophagy pathwayResearch in context EBioMedicine |
author_facet |
Chien-An Chu Chung-Ta Lee Jenq-Chang Lee Yi-Wen Wang Ching-Tang Huang Sheng-Hui Lan Peng-Chan Lin Bo-Wen Lin Yu-Feng Tian Hsiao-Sheng Liu Nan-Haw Chow |
author_sort |
Chien-An Chu |
title |
MiR-338-5p promotes metastasis of colorectal cancer by inhibition of phosphatidylinositol 3-kinase, catalytic subunit type 3-mediated autophagy pathwayResearch in context |
title_short |
MiR-338-5p promotes metastasis of colorectal cancer by inhibition of phosphatidylinositol 3-kinase, catalytic subunit type 3-mediated autophagy pathwayResearch in context |
title_full |
MiR-338-5p promotes metastasis of colorectal cancer by inhibition of phosphatidylinositol 3-kinase, catalytic subunit type 3-mediated autophagy pathwayResearch in context |
title_fullStr |
MiR-338-5p promotes metastasis of colorectal cancer by inhibition of phosphatidylinositol 3-kinase, catalytic subunit type 3-mediated autophagy pathwayResearch in context |
title_full_unstemmed |
MiR-338-5p promotes metastasis of colorectal cancer by inhibition of phosphatidylinositol 3-kinase, catalytic subunit type 3-mediated autophagy pathwayResearch in context |
title_sort |
mir-338-5p promotes metastasis of colorectal cancer by inhibition of phosphatidylinositol 3-kinase, catalytic subunit type 3-mediated autophagy pathwayresearch in context |
publisher |
Elsevier |
series |
EBioMedicine |
issn |
2352-3964 |
publishDate |
2019-05-01 |
description |
Background: In our preliminary screening, expression of miR-338-5p was found to be higher in primary colorectal cancer (CRC) with metastasis. The autophagy related gene- phosphatidylinositol 3-kinase, catalytic subunit type 3 (PIK3C3) appeared to be targeted by miR-338-5p. Here, we provide solid evidence in support of PIK3C3 involved in miR-338-5p related metastasis of CRC in vitro and in vivo. Methods: The potential clinical relevance of miR-338-5p and its target gene was analysed on benign colorectal polyps and primary CRCs by QPCR. Mouse spleen xenograft experiment was performed to examine the importance of miR-338-5p for metastasis. Findings: PIK3C3 was one of target genes of miR-338-5p. In primary CRCs, expression of miR-338-5p is positively related to tumour staging, distant metastasis and poor patient survival. Patients with higher ratios of miR-338-5p/PIK3C3 also had significantly poor overall survival, supporting their significance in the progression of CRC. Over-expression of miR-338-5p promotes CRC metastasis to the liver and lung in vivo, in which PIK3C3 was down-regulated in the metastatic tumours. In contrast, overexpression of PIK3C3 in miR-338-5p stable cells inhibited the growth of metastatic tumours. Both migration and invasion of CRC in vitro induced by miR-338-5p are mediated by suppression of PIK3C3. Using forward and reverse approaches, autophagy was proved to involve in CRC migration and invasion induced by miR-338-5p. Interpretation: MiR-338-5p induces migration, invasion and metastasis of CRC in part through PIK3C3-related autophagy pathway. The miR-338-5p/PIK3C3 ratio may become a prognostic biomarker for CRC patients. Fund: NCKU Hospital, Taiwan, Ministry of Science and Technology, Taiwan. Keywords: miR-338-5p, PIK3C3, Autophagy and colorectal cancer |
url |
http://www.sciencedirect.com/science/article/pii/S2352396419302440 |
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doaj-d76130558dfb4fbbae0b98e63c873fb32020-11-25T02:11:38ZengElsevierEBioMedicine2352-39642019-05-0143270281MiR-338-5p promotes metastasis of colorectal cancer by inhibition of phosphatidylinositol 3-kinase, catalytic subunit type 3-mediated autophagy pathwayResearch in contextChien-An Chu0Chung-Ta Lee1Jenq-Chang Lee2Yi-Wen Wang3Ching-Tang Huang4Sheng-Hui Lan5Peng-Chan Lin6Bo-Wen Lin7Yu-Feng Tian8Hsiao-Sheng Liu9Nan-Haw Chow10Institute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, TaiwanDepartment of Pathology, National Cheng Kung University Hospital, Taiwan; College of Medicine, National Cheng Kung University, Tainan, Taiwan; Department of Pathology, National Cheng Kung University Hospital Dou-Liou Branch, Douliou City, Yunlin County, TaiwanDepartment of Surgery, College of Medicine, National Cheng Kung University Hospital, Tainan, TaiwanDepartment of Pathology, National Cheng Kung University Hospital, Taiwan; College of Medicine, National Cheng Kung University, Tainan, TaiwanInstitute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, TaiwanInstitute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, Taiwan; Department of Life Sciences and Institute of Genome Sciences, National Yang-Ming University, Taipei, TaiwanDepartment of Internal Medicine, College of Medicine, National Cheng Kung University, Tainan, TaiwanDepartment of Surgery, College of Medicine, National Cheng Kung University Hospital, Tainan, TaiwanDepartment of Health & Nutrition, Chia Nan University of Pharmacy and Science, Tainan, Taiwan; Division of Colorectal Surgery, Department of Surgery, Chi Mei Medical Center, Tainan, TaiwanInstitute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, Taiwan; Department of Microbiology and Immunology, College of Medicine, National Cheng Kung University, Taiwan; Corresponding authors at: Department of Microbiology and Immunology, College of Medicine, National Cheng Kung University, No.1, University Road, Tainan City 701, Taiwan.Institute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, Taiwan; Department of Pathology, National Cheng Kung University Hospital, Taiwan; College of Medicine, National Cheng Kung University, Tainan, Taiwan; Corresponding authors at: Department of Pathology, College of Medicine, National Cheng Kung University, No.1, University Road, Tainan City 701, Taiwan.Background: In our preliminary screening, expression of miR-338-5p was found to be higher in primary colorectal cancer (CRC) with metastasis. The autophagy related gene- phosphatidylinositol 3-kinase, catalytic subunit type 3 (PIK3C3) appeared to be targeted by miR-338-5p. Here, we provide solid evidence in support of PIK3C3 involved in miR-338-5p related metastasis of CRC in vitro and in vivo. Methods: The potential clinical relevance of miR-338-5p and its target gene was analysed on benign colorectal polyps and primary CRCs by QPCR. Mouse spleen xenograft experiment was performed to examine the importance of miR-338-5p for metastasis. Findings: PIK3C3 was one of target genes of miR-338-5p. In primary CRCs, expression of miR-338-5p is positively related to tumour staging, distant metastasis and poor patient survival. Patients with higher ratios of miR-338-5p/PIK3C3 also had significantly poor overall survival, supporting their significance in the progression of CRC. Over-expression of miR-338-5p promotes CRC metastasis to the liver and lung in vivo, in which PIK3C3 was down-regulated in the metastatic tumours. In contrast, overexpression of PIK3C3 in miR-338-5p stable cells inhibited the growth of metastatic tumours. Both migration and invasion of CRC in vitro induced by miR-338-5p are mediated by suppression of PIK3C3. Using forward and reverse approaches, autophagy was proved to involve in CRC migration and invasion induced by miR-338-5p. Interpretation: MiR-338-5p induces migration, invasion and metastasis of CRC in part through PIK3C3-related autophagy pathway. The miR-338-5p/PIK3C3 ratio may become a prognostic biomarker for CRC patients. Fund: NCKU Hospital, Taiwan, Ministry of Science and Technology, Taiwan. Keywords: miR-338-5p, PIK3C3, Autophagy and colorectal cancerhttp://www.sciencedirect.com/science/article/pii/S2352396419302440 |