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Glyoxalase-I Is a Novel Prognosis Factor Associated with Gastric Cancer Progression

Glyoxalase I (GLO1), a methylglyoxal detoxification enzyme, is implicated in the progression of human malignancies. The role of GLO1 in gastric cancer development or progression is currently unclear. The expression of GLO1 was determined in primary gastric cancer specimens using quantitative polymer...

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Autores principales: Cheng, Wan-Li, Tsai, Ming-Ming, Tsai, Chung-Ying, Huang, Ya-Hui, Chen, Cheng-Yi, Chi, Hsiang-Cheng, Tseng, Yi-Hsin, Chao, Im-Wai, Lin, Wei-Chi, Wu, Sheng-Ming, Liang, Ying, Liao, Chia-Jung, Lin, Yang-Hsiang, Chung, I-Hsiao, Chen, Wei-Jan, Lin, Paul Y., Wang, Chia-Siu, Lin, Kwang-Huei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315534/
https://www.ncbi.nlm.nih.gov/pubmed/22479608
http://dx.doi.org/10.1371/journal.pone.0034352
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author Cheng, Wan-Li
Tsai, Ming-Ming
Tsai, Chung-Ying
Huang, Ya-Hui
Chen, Cheng-Yi
Chi, Hsiang-Cheng
Tseng, Yi-Hsin
Chao, Im-Wai
Lin, Wei-Chi
Wu, Sheng-Ming
Liang, Ying
Liao, Chia-Jung
Lin, Yang-Hsiang
Chung, I-Hsiao
Chen, Wei-Jan
Lin, Paul Y.
Wang, Chia-Siu
Lin, Kwang-Huei
author_facet Cheng, Wan-Li
Tsai, Ming-Ming
Tsai, Chung-Ying
Huang, Ya-Hui
Chen, Cheng-Yi
Chi, Hsiang-Cheng
Tseng, Yi-Hsin
Chao, Im-Wai
Lin, Wei-Chi
Wu, Sheng-Ming
Liang, Ying
Liao, Chia-Jung
Lin, Yang-Hsiang
Chung, I-Hsiao
Chen, Wei-Jan
Lin, Paul Y.
Wang, Chia-Siu
Lin, Kwang-Huei
author_sort Cheng, Wan-Li
collection PubMed
description Glyoxalase I (GLO1), a methylglyoxal detoxification enzyme, is implicated in the progression of human malignancies. The role of GLO1 in gastric cancer development or progression is currently unclear. The expression of GLO1 was determined in primary gastric cancer specimens using quantitative polymerase chain reaction, immunohistochemistry (IHC), and western blotting analyses. GLO1 expression was higher in gastric cancer tissues, compared with that in adjacent noncancerous tissues. Elevated expression of GLO1 was significantly associated with gastric wall invasion, lymph node metastasis, and pathological stage, suggesting a novel role of GLO1 in gastric cancer development and progression. The 5-year survival rate of the lower GLO1 expression groups was significantly greater than that of the higher expression groups (log rank P = 0.0373) in IHC experiments. Over-expression of GLO1 in gastric cancer cell lines increases cell proliferation, migration and invasiveness. Conversely, down-regulation of GLO1 with shRNA led to a marked reduction in the migration and invasion abilities. Our data strongly suggest that high expression of GLO1 in gastric cancer enhances the metastasis ability of tumor cells in vitro and in vivo, and support its efficacy as a potential marker for the detection and prognosis of gastric cancer.
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spelling pubmed-33155342012-04-04 Glyoxalase-I Is a Novel Prognosis Factor Associated with Gastric Cancer Progression Cheng, Wan-Li Tsai, Ming-Ming Tsai, Chung-Ying Huang, Ya-Hui Chen, Cheng-Yi Chi, Hsiang-Cheng Tseng, Yi-Hsin Chao, Im-Wai Lin, Wei-Chi Wu, Sheng-Ming Liang, Ying Liao, Chia-Jung Lin, Yang-Hsiang Chung, I-Hsiao Chen, Wei-Jan Lin, Paul Y. Wang, Chia-Siu Lin, Kwang-Huei PLoS One Research Article Glyoxalase I (GLO1), a methylglyoxal detoxification enzyme, is implicated in the progression of human malignancies. The role of GLO1 in gastric cancer development or progression is currently unclear. The expression of GLO1 was determined in primary gastric cancer specimens using quantitative polymerase chain reaction, immunohistochemistry (IHC), and western blotting analyses. GLO1 expression was higher in gastric cancer tissues, compared with that in adjacent noncancerous tissues. Elevated expression of GLO1 was significantly associated with gastric wall invasion, lymph node metastasis, and pathological stage, suggesting a novel role of GLO1 in gastric cancer development and progression. The 5-year survival rate of the lower GLO1 expression groups was significantly greater than that of the higher expression groups (log rank P = 0.0373) in IHC experiments. Over-expression of GLO1 in gastric cancer cell lines increases cell proliferation, migration and invasiveness. Conversely, down-regulation of GLO1 with shRNA led to a marked reduction in the migration and invasion abilities. Our data strongly suggest that high expression of GLO1 in gastric cancer enhances the metastasis ability of tumor cells in vitro and in vivo, and support its efficacy as a potential marker for the detection and prognosis of gastric cancer. Public Library of Science 2012-03-29 /pmc/articles/PMC3315534/ /pubmed/22479608 http://dx.doi.org/10.1371/journal.pone.0034352 Text en Cheng et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cheng, Wan-Li
Tsai, Ming-Ming
Tsai, Chung-Ying
Huang, Ya-Hui
Chen, Cheng-Yi
Chi, Hsiang-Cheng
Tseng, Yi-Hsin
Chao, Im-Wai
Lin, Wei-Chi
Wu, Sheng-Ming
Liang, Ying
Liao, Chia-Jung
Lin, Yang-Hsiang
Chung, I-Hsiao
Chen, Wei-Jan
Lin, Paul Y.
Wang, Chia-Siu
Lin, Kwang-Huei
Glyoxalase-I Is a Novel Prognosis Factor Associated with Gastric Cancer Progression
title Glyoxalase-I Is a Novel Prognosis Factor Associated with Gastric Cancer Progression
title_full Glyoxalase-I Is a Novel Prognosis Factor Associated with Gastric Cancer Progression
title_fullStr Glyoxalase-I Is a Novel Prognosis Factor Associated with Gastric Cancer Progression
title_full_unstemmed Glyoxalase-I Is a Novel Prognosis Factor Associated with Gastric Cancer Progression
title_short Glyoxalase-I Is a Novel Prognosis Factor Associated with Gastric Cancer Progression
title_sort glyoxalase-i is a novel prognosis factor associated with gastric cancer progression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315534/
https://www.ncbi.nlm.nih.gov/pubmed/22479608
http://dx.doi.org/10.1371/journal.pone.0034352
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