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Expression of HIWI in human esophageal squamous cell carcinoma is significantly associated with poorer prognosis

BACKGROUND: HIWI, the human homologue of Piwi family, is present in CD34(+ )hematopoietic stem cells and germ cells, but not in well-differentiated cell populations, indicating that HIWI may play an impotent role in determining or maintaining stemness of these cells. That HIWI expression has been de...

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Autores principales: He, Wei, Wang, Zhihui, Wang, Qi, Fan, Qingxia, Shou, Chengcao, Wang, Junsheng, Giercksky, Karl-Erik, Nesland, Jahn M, Suo, Zhenhe
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2801519/
https://www.ncbi.nlm.nih.gov/pubmed/19995427
http://dx.doi.org/10.1186/1471-2407-9-426
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author He, Wei
Wang, Zhihui
Wang, Qi
Fan, Qingxia
Shou, Chengcao
Wang, Junsheng
Giercksky, Karl-Erik
Nesland, Jahn M
Suo, Zhenhe
author_facet He, Wei
Wang, Zhihui
Wang, Qi
Fan, Qingxia
Shou, Chengcao
Wang, Junsheng
Giercksky, Karl-Erik
Nesland, Jahn M
Suo, Zhenhe
author_sort He, Wei
collection PubMed
description BACKGROUND: HIWI, the human homologue of Piwi family, is present in CD34(+ )hematopoietic stem cells and germ cells, but not in well-differentiated cell populations, indicating that HIWI may play an impotent role in determining or maintaining stemness of these cells. That HIWI expression has been detected in several type tumours may suggest its association with clinical outcome in cancer patients. METHODS: With the methods of real-time PCR, western blot, immunocytochemistry and immunohistochemistry, the expression of HIWI in three esophageal squamous cancer cell lines KYSE70, KYSE140 and KYSE450 has been characterized. Then, we investigated HIWI expression in a series of 153 esophageal squamous cell carcinomas using immunohistochemistry and explored its association with clinicopathological features. RESULTS: The expression of HIWI was observed in tumour cell nuclei or/and cytoplasm in 137 (89.5%) cases, 16 (10.5%) cases were negative in both nuclei and cytoplasm. 86 (56.2%) were strongly positive in cytoplasm, while 49 (32.0%) were strongly positive in nuclei. The expression level of HIWI in cytoplasm of esophageal cancer cells was significantly associated with histological grade (P = 0.011), T stage (P = 0.035), and clinic outcome (P < 0.001), while there was no correlation between the nuclear HIWI expression and clinicopathological features. CONCLUSION: The expression of HIWI in the cytoplasm of esophageal cancer cells is significantly associated with higher histological grade, clinical stage and poorer clinical outcome, indicating its possible involvement in cancer development.
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spelling pubmed-28015192010-01-05 Expression of HIWI in human esophageal squamous cell carcinoma is significantly associated with poorer prognosis He, Wei Wang, Zhihui Wang, Qi Fan, Qingxia Shou, Chengcao Wang, Junsheng Giercksky, Karl-Erik Nesland, Jahn M Suo, Zhenhe BMC Cancer Research Article BACKGROUND: HIWI, the human homologue of Piwi family, is present in CD34(+ )hematopoietic stem cells and germ cells, but not in well-differentiated cell populations, indicating that HIWI may play an impotent role in determining or maintaining stemness of these cells. That HIWI expression has been detected in several type tumours may suggest its association with clinical outcome in cancer patients. METHODS: With the methods of real-time PCR, western blot, immunocytochemistry and immunohistochemistry, the expression of HIWI in three esophageal squamous cancer cell lines KYSE70, KYSE140 and KYSE450 has been characterized. Then, we investigated HIWI expression in a series of 153 esophageal squamous cell carcinomas using immunohistochemistry and explored its association with clinicopathological features. RESULTS: The expression of HIWI was observed in tumour cell nuclei or/and cytoplasm in 137 (89.5%) cases, 16 (10.5%) cases were negative in both nuclei and cytoplasm. 86 (56.2%) were strongly positive in cytoplasm, while 49 (32.0%) were strongly positive in nuclei. The expression level of HIWI in cytoplasm of esophageal cancer cells was significantly associated with histological grade (P = 0.011), T stage (P = 0.035), and clinic outcome (P < 0.001), while there was no correlation between the nuclear HIWI expression and clinicopathological features. CONCLUSION: The expression of HIWI in the cytoplasm of esophageal cancer cells is significantly associated with higher histological grade, clinical stage and poorer clinical outcome, indicating its possible involvement in cancer development. BioMed Central 2009-12-08 /pmc/articles/PMC2801519/ /pubmed/19995427 http://dx.doi.org/10.1186/1471-2407-9-426 Text en Copyright ©2009 He et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
He, Wei
Wang, Zhihui
Wang, Qi
Fan, Qingxia
Shou, Chengcao
Wang, Junsheng
Giercksky, Karl-Erik
Nesland, Jahn M
Suo, Zhenhe
Expression of HIWI in human esophageal squamous cell carcinoma is significantly associated with poorer prognosis
title Expression of HIWI in human esophageal squamous cell carcinoma is significantly associated with poorer prognosis
title_full Expression of HIWI in human esophageal squamous cell carcinoma is significantly associated with poorer prognosis
title_fullStr Expression of HIWI in human esophageal squamous cell carcinoma is significantly associated with poorer prognosis
title_full_unstemmed Expression of HIWI in human esophageal squamous cell carcinoma is significantly associated with poorer prognosis
title_short Expression of HIWI in human esophageal squamous cell carcinoma is significantly associated with poorer prognosis
title_sort expression of hiwi in human esophageal squamous cell carcinoma is significantly associated with poorer prognosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2801519/
https://www.ncbi.nlm.nih.gov/pubmed/19995427
http://dx.doi.org/10.1186/1471-2407-9-426
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