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Article: Cytoplasmic Forkhead Box M1 (FoxM1) in Esophageal Squamous Cell Carcinoma Significantly Correlates with Pathological Disease Stage
Title | Cytoplasmic Forkhead Box M1 (FoxM1) in Esophageal Squamous Cell Carcinoma Significantly Correlates with Pathological Disease Stage |
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Authors | |
Keywords | Vascular Surgery Thoracic Surgery General Surgery Cardiac Surgery Abdominal Surgery Surgery Medicine & Public Health |
Issue Date | 2011 |
Publisher | Springer New York LLC. The Journal's web site is located at http://link.springer.de/link/service/journals/00268/ |
Citation | World Journal Of Surgery, 2011, p. 1-8 How to Cite? |
Abstract | Abstract: Esophageal cancer is a deadly cancer with esophageal squamous cell carcinoma (ESCC) as the major type. Until now there has been a lack of reliable prognostic markers for this malignancy. This study aims to investigate the clinical correlation between Forkhead box M1 (FoxM1) and patients' parameters in ESCC. Methods: Immunohistochemistry was performed to investigate the expression and localization of FoxM1 in 64 ESCC tissues and 10 nontumor esophageal tissues randomly selected from 64 patients before these data were used for clinical correlations. Results: Cytoplasmic and nuclear expressions of FoxM1 were found in 63 and 16 of the 64 ESCC tissues, respectively. Low cytoplasmic expression of FoxM1 was correlated with early pathological stage in ESCC (P = 0.018), while patients with nuclear FoxM1 were younger in age than those without nuclear expression (P < 0.001). Upregulation of FoxM1 mRNA was found in five ESCC cell lines (HKESC-1, HKESC-2, HKESC-3, HKESC-4, and SLMT-1) when compared to non-neoplastic esophageal squamous cell line NE-1 using quantitative polymerase chain reaction (qPCR). Except for HKESC-3, all studied ESCC cell lines demonstrated a high expression of FoxM1 protein using immunoblot. A high mRNA level of FoxM1 was observed in all of the ESCC tissues examined when compared to their adjacent nontumor tissues using qPCR. Conclusion: Cytoplasmic FoxM1 was correlated with pathological stage and might be a biomarker for advanced ESCC. © 2011 The Author(s). |
Persistent Identifier | http://hdl.handle.net/10722/144939 |
ISSN | 2023 Impact Factor: 2.3 2023 SCImago Journal Rankings: 0.772 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Hui, MKC | en_HK |
dc.contributor.author | Chan, KW | en_HK |
dc.contributor.author | Luk, JM | en_HK |
dc.contributor.author | Lee, NP | en_HK |
dc.contributor.author | Chung, Y | en_HK |
dc.contributor.author | Cheung, LCM | en_HK |
dc.contributor.author | Srivastava, G | en_HK |
dc.contributor.author | Tsao, SW | en_HK |
dc.contributor.author | Tang, JC | en_HK |
dc.contributor.author | Law, S | en_HK |
dc.date.accessioned | 2012-02-21T05:43:13Z | - |
dc.date.available | 2012-02-21T05:43:13Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | World Journal Of Surgery, 2011, p. 1-8 | en_HK |
dc.identifier.issn | 0364-2313 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/144939 | - |
dc.description.abstract | Abstract: Esophageal cancer is a deadly cancer with esophageal squamous cell carcinoma (ESCC) as the major type. Until now there has been a lack of reliable prognostic markers for this malignancy. This study aims to investigate the clinical correlation between Forkhead box M1 (FoxM1) and patients' parameters in ESCC. Methods: Immunohistochemistry was performed to investigate the expression and localization of FoxM1 in 64 ESCC tissues and 10 nontumor esophageal tissues randomly selected from 64 patients before these data were used for clinical correlations. Results: Cytoplasmic and nuclear expressions of FoxM1 were found in 63 and 16 of the 64 ESCC tissues, respectively. Low cytoplasmic expression of FoxM1 was correlated with early pathological stage in ESCC (P = 0.018), while patients with nuclear FoxM1 were younger in age than those without nuclear expression (P < 0.001). Upregulation of FoxM1 mRNA was found in five ESCC cell lines (HKESC-1, HKESC-2, HKESC-3, HKESC-4, and SLMT-1) when compared to non-neoplastic esophageal squamous cell line NE-1 using quantitative polymerase chain reaction (qPCR). Except for HKESC-3, all studied ESCC cell lines demonstrated a high expression of FoxM1 protein using immunoblot. A high mRNA level of FoxM1 was observed in all of the ESCC tissues examined when compared to their adjacent nontumor tissues using qPCR. Conclusion: Cytoplasmic FoxM1 was correlated with pathological stage and might be a biomarker for advanced ESCC. © 2011 The Author(s). | en_HK |
dc.language | eng | en_US |
dc.publisher | Springer New York LLC. The Journal's web site is located at http://link.springer.de/link/service/journals/00268/ | en_HK |
dc.relation.ispartof | World Journal of Surgery | en_HK |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | en_US |
dc.subject | Vascular Surgery | en_US |
dc.subject | Thoracic Surgery | en_US |
dc.subject | General Surgery | en_US |
dc.subject | Cardiac Surgery | en_US |
dc.subject | Abdominal Surgery | en_US |
dc.subject | Surgery | en_US |
dc.subject | Medicine & Public Health | en_US |
dc.title | Cytoplasmic Forkhead Box M1 (FoxM1) in Esophageal Squamous Cell Carcinoma Significantly Correlates with Pathological Disease Stage | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Chan, KW: hrmtckw@hku.hk | en_HK |
dc.identifier.email | Luk, JM: jmluk@hkucc.hku.hk | en_HK |
dc.identifier.email | Lee, NP: nikkilee@hku.hk | en_HK |
dc.identifier.email | Srivastava, G: gopesh@pathology.hku.hk | en_HK |
dc.identifier.email | Tsao, SW: gswtsao@hkucc.hku.hk | en_HK |
dc.identifier.email | Law, S: slaw@hku.hk | en_HK |
dc.identifier.authority | Chan, KW=rp00330 | en_HK |
dc.identifier.authority | Luk, JM=rp00349 | en_HK |
dc.identifier.authority | Lee, NP=rp00263 | en_HK |
dc.identifier.authority | Srivastava, G=rp00365 | en_HK |
dc.identifier.authority | Tsao, SW=rp00399 | en_HK |
dc.identifier.authority | Law, S=rp00437 | en_HK |
dc.description.nature | published_or_final_version | en_US |
dc.identifier.doi | 10.1007/s00268-011-1302-5 | en_HK |
dc.identifier.pmid | 21976009 | - |
dc.identifier.pmcid | PMC3243851 | - |
dc.identifier.scopus | eid_2-s2.0-84866005592 | en_HK |
dc.identifier.hkuros | 198774 | - |
dc.identifier.volume | 36 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.spage | 1 | en_HK |
dc.identifier.epage | 8 | en_HK |
dc.identifier.eissn | 1432-2323 | en_US |
dc.identifier.isi | WOS:000298328600012 | - |
dc.publisher.place | United States | en_HK |
dc.description.other | Springer Open Choice, 21 Feb 2012 | en_US |
dc.identifier.scopusauthorid | Hui, MKC=8644138500 | en_HK |
dc.identifier.scopusauthorid | Chan, KW=16444133100 | en_HK |
dc.identifier.scopusauthorid | Luk, JM=7006777791 | en_HK |
dc.identifier.scopusauthorid | Lee, NP=7402722690 | en_HK |
dc.identifier.scopusauthorid | Chung, Y=22833625500 | en_HK |
dc.identifier.scopusauthorid | Cheung, LCM=21740536900 | en_HK |
dc.identifier.scopusauthorid | Srivastava, G=7202242238 | en_HK |
dc.identifier.scopusauthorid | Tsao, SW=7102813116 | en_HK |
dc.identifier.scopusauthorid | Tang, JC=14056850300 | en_HK |
dc.identifier.scopusauthorid | Law, S=7202241293 | en_HK |
dc.identifier.citeulike | 9893650 | - |
dc.identifier.issnl | 0364-2313 | - |