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- PMID: 11206273
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Article: A comparative study of the clinicopathological significance of E-cadherin and catenins (α, β, γ) expression in the surgical management of oral tongue carcinoma
Title | A comparative study of the clinicopathological significance of E-cadherin and catenins (α, β, γ) expression in the surgical management of oral tongue carcinoma |
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Authors | |
Keywords | Carcinoma Catenin E-cadherin Oral Tongue |
Issue Date | 2001 |
Publisher | Springer Verlag. The Journal's web site is located at http://link.springer.de/link/service/journals/00432/index.htm |
Citation | Journal Of Cancer Research And Clinical Oncology, 2001, v. 127 n. 1, p. 59-63 How to Cite? |
Abstract | Purpose: E-cadherin and catenins are important epithelial adhesion molecules in normal epithelium. Loss of E-cadherin-catenin adhesion is an important step in the progression of many epithelial cancers. E-cadherin and catenins expression in carcinoma of the tongue were evaluated in relation to their clinicopathological features and prognostic values. Method: Immunohistochemical staining was carried out with E-cadherin and (α, β, γ)-catenin monoclonal antibodies for 85 surgical specimens of oral tongue carcinoma, nine matched metastatic lymph nodes, and seven locally recurrent tumours. Results: There was under-expression in 85% of E-cadherin, 94% of α-catenin, 89% of β-catenin, and 83% of γ-catenin in the primary tumours. There was no correlation of E-cadherin/catenin expression with sex, age, cancer stage, and differentiation. Nodal metastasis was found in 68% of patients with weak expression of γ-catenin compared with 9% with strong expression in primary tumours (chi-square, P = 0.02). E-cadherin was a significant prognostic factor for survival and recurrence; patients with weak E-cadherin expression had 53% 5-year survival compared with 85% with strong expression (Wilcoxon, P = 0.0159). Conclusions: Both E-cadherin and catenins were highly under-expressed in oral tongue carcinoma, metastatic lymph node, and recurrent tumour. γ-catenin had predictive value for nodal metastasis. E-cadherin was, however, a more important prognostic factor for recurrence and survival. |
Persistent Identifier | http://hdl.handle.net/10722/149597 |
ISSN | 2023 Impact Factor: 2.7 2023 SCImago Journal Rankings: 1.023 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chow, V | en_HK |
dc.contributor.author | Wing Yuen, AP | en_HK |
dc.contributor.author | Lam, KY | en_HK |
dc.contributor.author | Wah Tsao, GS | en_HK |
dc.contributor.author | Ho, WK | en_HK |
dc.contributor.author | Wei, WI | en_HK |
dc.date.accessioned | 2012-06-26T05:55:43Z | - |
dc.date.available | 2012-06-26T05:55:43Z | - |
dc.date.issued | 2001 | en_HK |
dc.identifier.citation | Journal Of Cancer Research And Clinical Oncology, 2001, v. 127 n. 1, p. 59-63 | en_HK |
dc.identifier.issn | 0171-5216 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/149597 | - |
dc.description.abstract | Purpose: E-cadherin and catenins are important epithelial adhesion molecules in normal epithelium. Loss of E-cadherin-catenin adhesion is an important step in the progression of many epithelial cancers. E-cadherin and catenins expression in carcinoma of the tongue were evaluated in relation to their clinicopathological features and prognostic values. Method: Immunohistochemical staining was carried out with E-cadherin and (α, β, γ)-catenin monoclonal antibodies for 85 surgical specimens of oral tongue carcinoma, nine matched metastatic lymph nodes, and seven locally recurrent tumours. Results: There was under-expression in 85% of E-cadherin, 94% of α-catenin, 89% of β-catenin, and 83% of γ-catenin in the primary tumours. There was no correlation of E-cadherin/catenin expression with sex, age, cancer stage, and differentiation. Nodal metastasis was found in 68% of patients with weak expression of γ-catenin compared with 9% with strong expression in primary tumours (chi-square, P = 0.02). E-cadherin was a significant prognostic factor for survival and recurrence; patients with weak E-cadherin expression had 53% 5-year survival compared with 85% with strong expression (Wilcoxon, P = 0.0159). Conclusions: Both E-cadherin and catenins were highly under-expressed in oral tongue carcinoma, metastatic lymph node, and recurrent tumour. γ-catenin had predictive value for nodal metastasis. E-cadherin was, however, a more important prognostic factor for recurrence and survival. | en_HK |
dc.language | eng | en_US |
dc.publisher | Springer Verlag. The Journal's web site is located at http://link.springer.de/link/service/journals/00432/index.htm | en_HK |
dc.relation.ispartof | Journal of Cancer Research and Clinical Oncology | en_HK |
dc.subject | Carcinoma | en_HK |
dc.subject | Catenin | en_HK |
dc.subject | E-cadherin | en_HK |
dc.subject | Oral | en_HK |
dc.subject | Tongue | en_HK |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Aged, 80 And Over | en_US |
dc.subject.mesh | Cadherins - Biosynthesis | en_US |
dc.subject.mesh | Carcinoma - Diagnosis - Metabolism - Mortality | en_US |
dc.subject.mesh | Cytoskeletal Proteins - Biosynthesis | en_US |
dc.subject.mesh | Desmoplakins | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Head And Neck Neoplasms - Metabolism | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Immunohistochemistry | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Prognosis | en_US |
dc.subject.mesh | Tongue Neoplasms - Diagnosis - Metabolism - Mortality | en_US |
dc.subject.mesh | Trans-Activators | en_US |
dc.subject.mesh | Alpha Catenin | en_US |
dc.subject.mesh | Beta Catenin | en_US |
dc.subject.mesh | Gamma Catenin | en_US |
dc.title | A comparative study of the clinicopathological significance of E-cadherin and catenins (α, β, γ) expression in the surgical management of oral tongue carcinoma | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Wah Tsao, GS: gswtsao@hkucc.hku.hk | en_HK |
dc.identifier.email | Wei, WI: hrmswwi@hku.hk | en_HK |
dc.identifier.authority | Wah Tsao, GS=rp00399 | en_HK |
dc.identifier.authority | Wei, WI=rp00323 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1007/s004320000177 | en_HK |
dc.identifier.pmid | 11206273 | - |
dc.identifier.scopus | eid_2-s2.0-0034744325 | en_HK |
dc.identifier.hkuros | 56511 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0034744325&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 127 | en_HK |
dc.identifier.issue | 1 | en_HK |
dc.identifier.spage | 59 | en_HK |
dc.identifier.epage | 63 | en_HK |
dc.identifier.isi | WOS:000166508100009 | - |
dc.publisher.place | Germany | en_HK |
dc.identifier.scopusauthorid | Chow, V=7006616213 | en_HK |
dc.identifier.scopusauthorid | Wing Yuen, AP=15824563100 | en_HK |
dc.identifier.scopusauthorid | Lam, KY=7403657165 | en_HK |
dc.identifier.scopusauthorid | Wah Tsao, GS=7102813116 | en_HK |
dc.identifier.scopusauthorid | Ho, WK=7402968844 | en_HK |
dc.identifier.scopusauthorid | Wei, WI=7403321552 | en_HK |
dc.identifier.issnl | 0171-5216 | - |