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RNA-binding protein KHSRP promotes tumor growth and metastasis in non-small cell lung cancer
BACKGROUND: KH-type splicing regulatory protein (KHSRP) plays an important role in cancer invasion, but the relevant mechanism is not well known. In the present study, we investigated the function and potential molecular mechanism of KHSRP in non-small cell lung cancer (NSCLC) metastasis and elucida...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882349/ https://www.ncbi.nlm.nih.gov/pubmed/31775888 http://dx.doi.org/10.1186/s13046-019-1479-2 |
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author | Yan, Mingxia Sun, Lei Li, Jing Yu, Huajian Lin, Hechun Yu, Tao Zhao, Fangyu Zhu, Miaoxin Liu, Lei Geng, Qin Kong, Hanwei Pan, Hongyu Yao, Ming |
author_facet | Yan, Mingxia Sun, Lei Li, Jing Yu, Huajian Lin, Hechun Yu, Tao Zhao, Fangyu Zhu, Miaoxin Liu, Lei Geng, Qin Kong, Hanwei Pan, Hongyu Yao, Ming |
author_sort | Yan, Mingxia |
collection | PubMed |
description | BACKGROUND: KH-type splicing regulatory protein (KHSRP) plays an important role in cancer invasion, but the relevant mechanism is not well known. In the present study, we investigated the function and potential molecular mechanism of KHSRP in non-small cell lung cancer (NSCLC) metastasis and elucidated its clinical significance. METHODS: Isobaric tags for relative and absolute quantitation and the SWATH™ approach were combined with nanoliquid chromatography-tandem mass spectrometry analysis to identify metastasis-associated nucleoproteins in NSCLC. Real-time PCR and Western blot were used to screen for metastasis-associated candidate molecules. Gene knockdown and overexpression were used to investigate their functions and molecular mechanisms in lung cancer cells. Coimmunoprecipitation (Co-IP) experiments were performed to identify the interactions between candidate molecules and their interacting proteins. Gene expression and its association with multiple clinicopathologic characteristics were analyzed by immunohistochemistry (IHC) and Western blot in human lung cancer specimens. RESULTS: KHSRP was identified as a metastasis-associated candidate molecule. In NSCLC cell lines, knockdown of KHSRP significantly reduced lung cancer cell proliferation, migration, and invasion in vitro and in vivo, whereas overexpression of KHSRP did the opposite. Mechanistically, the protein heterogeneous nuclear ribonucleoprotein C (C1/C2) (HNRNPC) was identified to interact with KHSRP using Co-IP experiments. In NSCLC cell lines, overexpression of HNRNPC significantly promoted lung cancer cell proliferation, migration, and invasion in vitro and in vivo. KHSRP and HNRNPC may induce human lung cancer cell invasion and metastasis by activating the IFN-α-JAK-STAT1 signaling pathway. Drastically higher expression levels of KHSRP and HNRNPC were observed in lung cancer tissues compared to those in adjacent noncancerous tissues. Increased KHSRP and HNRNPC expression was significantly associated with advanced tumor stages and metastasis (both lymph node and distant). Kaplan-Meier survival analysis showed that patients with high KHSRP and HNRNPC expression levels were predicted to have the shortest survival times and to have a poor prognosis. CONCLUSIONS: KHSRP plays an important role in NSCLC metastasis and may serve as a potential prognostic marker and novel therapeutic target for lung cancer metastasis treatment. |
format | Online Article Text |
id | pubmed-6882349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68823492019-12-03 RNA-binding protein KHSRP promotes tumor growth and metastasis in non-small cell lung cancer Yan, Mingxia Sun, Lei Li, Jing Yu, Huajian Lin, Hechun Yu, Tao Zhao, Fangyu Zhu, Miaoxin Liu, Lei Geng, Qin Kong, Hanwei Pan, Hongyu Yao, Ming J Exp Clin Cancer Res Research BACKGROUND: KH-type splicing regulatory protein (KHSRP) plays an important role in cancer invasion, but the relevant mechanism is not well known. In the present study, we investigated the function and potential molecular mechanism of KHSRP in non-small cell lung cancer (NSCLC) metastasis and elucidated its clinical significance. METHODS: Isobaric tags for relative and absolute quantitation and the SWATH™ approach were combined with nanoliquid chromatography-tandem mass spectrometry analysis to identify metastasis-associated nucleoproteins in NSCLC. Real-time PCR and Western blot were used to screen for metastasis-associated candidate molecules. Gene knockdown and overexpression were used to investigate their functions and molecular mechanisms in lung cancer cells. Coimmunoprecipitation (Co-IP) experiments were performed to identify the interactions between candidate molecules and their interacting proteins. Gene expression and its association with multiple clinicopathologic characteristics were analyzed by immunohistochemistry (IHC) and Western blot in human lung cancer specimens. RESULTS: KHSRP was identified as a metastasis-associated candidate molecule. In NSCLC cell lines, knockdown of KHSRP significantly reduced lung cancer cell proliferation, migration, and invasion in vitro and in vivo, whereas overexpression of KHSRP did the opposite. Mechanistically, the protein heterogeneous nuclear ribonucleoprotein C (C1/C2) (HNRNPC) was identified to interact with KHSRP using Co-IP experiments. In NSCLC cell lines, overexpression of HNRNPC significantly promoted lung cancer cell proliferation, migration, and invasion in vitro and in vivo. KHSRP and HNRNPC may induce human lung cancer cell invasion and metastasis by activating the IFN-α-JAK-STAT1 signaling pathway. Drastically higher expression levels of KHSRP and HNRNPC were observed in lung cancer tissues compared to those in adjacent noncancerous tissues. Increased KHSRP and HNRNPC expression was significantly associated with advanced tumor stages and metastasis (both lymph node and distant). Kaplan-Meier survival analysis showed that patients with high KHSRP and HNRNPC expression levels were predicted to have the shortest survival times and to have a poor prognosis. CONCLUSIONS: KHSRP plays an important role in NSCLC metastasis and may serve as a potential prognostic marker and novel therapeutic target for lung cancer metastasis treatment. BioMed Central 2019-11-27 /pmc/articles/PMC6882349/ /pubmed/31775888 http://dx.doi.org/10.1186/s13046-019-1479-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Yan, Mingxia Sun, Lei Li, Jing Yu, Huajian Lin, Hechun Yu, Tao Zhao, Fangyu Zhu, Miaoxin Liu, Lei Geng, Qin Kong, Hanwei Pan, Hongyu Yao, Ming RNA-binding protein KHSRP promotes tumor growth and metastasis in non-small cell lung cancer |
title | RNA-binding protein KHSRP promotes tumor growth and metastasis in non-small cell lung cancer |
title_full | RNA-binding protein KHSRP promotes tumor growth and metastasis in non-small cell lung cancer |
title_fullStr | RNA-binding protein KHSRP promotes tumor growth and metastasis in non-small cell lung cancer |
title_full_unstemmed | RNA-binding protein KHSRP promotes tumor growth and metastasis in non-small cell lung cancer |
title_short | RNA-binding protein KHSRP promotes tumor growth and metastasis in non-small cell lung cancer |
title_sort | rna-binding protein khsrp promotes tumor growth and metastasis in non-small cell lung cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882349/ https://www.ncbi.nlm.nih.gov/pubmed/31775888 http://dx.doi.org/10.1186/s13046-019-1479-2 |
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