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High kinesin family member 18A expression correlates with poor prognosis in primary lung adenocarcinoma
BACKGROUND: Lung adenocarcinoma (LUAD) is the most prevalent pathological subtype of lung cancer. Kinesin family member 18A (KIF18A) plays an important role in tumorigenesis. Its roles in breast cancer, colorectal cancer, and other tumors have been demonstrated; however, studies of KIF18A in LUAD ar...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6500977/ https://www.ncbi.nlm.nih.gov/pubmed/30907518 http://dx.doi.org/10.1111/1759-7714.13051 |
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author | Li, Xiaoqing Liu, Meirong Zhang, Zheng Zhang, Linlin Liang, Xingmei Sun, Linlin Zhong, Diansheng |
author_facet | Li, Xiaoqing Liu, Meirong Zhang, Zheng Zhang, Linlin Liang, Xingmei Sun, Linlin Zhong, Diansheng |
author_sort | Li, Xiaoqing |
collection | PubMed |
description | BACKGROUND: Lung adenocarcinoma (LUAD) is the most prevalent pathological subtype of lung cancer. Kinesin family member 18A (KIF18A) plays an important role in tumorigenesis. Its roles in breast cancer, colorectal cancer, and other tumors have been demonstrated; however, studies of KIF18A in LUAD are limited. This study aimed to determine the role of KIF18A in LUAD progression and prognostic prediction. METHODS: KIF18A expression was examined in LUAD cells and tissues by immunohistochemistry and Western blotting. Cell proliferation assay was performed to study the role of KIF18A in LUAD cells. Correlations between KIF18A expression and clinicopathological features were analyzed. The role of KIF18A in LUAD prognosis was evaluated using data from The Cancer Genome Atlas (TCGA). RESULTS: KIF18A expression was increased in tumor cells and tissues. Downregulation of KIF18A expression resulted in the suppression of cancer cell proliferation in in vitro assays, and was particularly related to poor tumor differentiation, big tumor size, lymph node metastasis, and more advanced tumor stage. In the TCGA dataset, high KIF18A messenger RNA expression was associated with poor disease‐free and overall survival in patients with LUAD. In addition, multivariate analysis indicated that KIF18A is an independent prognostic factor of disease‐free and overall survival in LUAD. CONCLUSIONS: Collectively, our results demonstrate that KIFl8A is highly expressed in LUAD. KIFl8A plays an important role in LUAD cell proliferation, but is a poor prognostic factor. |
format | Online Article Text |
id | pubmed-6500977 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-65009772019-05-10 High kinesin family member 18A expression correlates with poor prognosis in primary lung adenocarcinoma Li, Xiaoqing Liu, Meirong Zhang, Zheng Zhang, Linlin Liang, Xingmei Sun, Linlin Zhong, Diansheng Thorac Cancer Original Articles BACKGROUND: Lung adenocarcinoma (LUAD) is the most prevalent pathological subtype of lung cancer. Kinesin family member 18A (KIF18A) plays an important role in tumorigenesis. Its roles in breast cancer, colorectal cancer, and other tumors have been demonstrated; however, studies of KIF18A in LUAD are limited. This study aimed to determine the role of KIF18A in LUAD progression and prognostic prediction. METHODS: KIF18A expression was examined in LUAD cells and tissues by immunohistochemistry and Western blotting. Cell proliferation assay was performed to study the role of KIF18A in LUAD cells. Correlations between KIF18A expression and clinicopathological features were analyzed. The role of KIF18A in LUAD prognosis was evaluated using data from The Cancer Genome Atlas (TCGA). RESULTS: KIF18A expression was increased in tumor cells and tissues. Downregulation of KIF18A expression resulted in the suppression of cancer cell proliferation in in vitro assays, and was particularly related to poor tumor differentiation, big tumor size, lymph node metastasis, and more advanced tumor stage. In the TCGA dataset, high KIF18A messenger RNA expression was associated with poor disease‐free and overall survival in patients with LUAD. In addition, multivariate analysis indicated that KIF18A is an independent prognostic factor of disease‐free and overall survival in LUAD. CONCLUSIONS: Collectively, our results demonstrate that KIFl8A is highly expressed in LUAD. KIFl8A plays an important role in LUAD cell proliferation, but is a poor prognostic factor. John Wiley & Sons Australia, Ltd 2019-03-25 2019-05 /pmc/articles/PMC6500977/ /pubmed/30907518 http://dx.doi.org/10.1111/1759-7714.13051 Text en © 2019 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Li, Xiaoqing Liu, Meirong Zhang, Zheng Zhang, Linlin Liang, Xingmei Sun, Linlin Zhong, Diansheng High kinesin family member 18A expression correlates with poor prognosis in primary lung adenocarcinoma |
title | High kinesin family member 18A expression correlates with poor prognosis in primary lung adenocarcinoma |
title_full | High kinesin family member 18A expression correlates with poor prognosis in primary lung adenocarcinoma |
title_fullStr | High kinesin family member 18A expression correlates with poor prognosis in primary lung adenocarcinoma |
title_full_unstemmed | High kinesin family member 18A expression correlates with poor prognosis in primary lung adenocarcinoma |
title_short | High kinesin family member 18A expression correlates with poor prognosis in primary lung adenocarcinoma |
title_sort | high kinesin family member 18a expression correlates with poor prognosis in primary lung adenocarcinoma |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6500977/ https://www.ncbi.nlm.nih.gov/pubmed/30907518 http://dx.doi.org/10.1111/1759-7714.13051 |
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