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CD44/CD24 Expression in recurrent gastric cancer: a retrospective analysis

BACKGROUND: To correlate CD44/CD24 expression with gastric cancer recurrence and prognosis. Gastric cancer is the second leading cause of cancer mortality due to the high recurrence rate, of which the molecular signature has not yet been identified. METHODS: We retrospectively reviewed the hospital...

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Autores principales: Yong, Ching-Shya, Ou Yang, Chih-Ming, Chou, Yenn-Hwei, Liao, Chao-Sheng, Lee, Chung-Wei, Lee, Chin-Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3444408/
https://www.ncbi.nlm.nih.gov/pubmed/22839505
http://dx.doi.org/10.1186/1471-230X-12-95
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author Yong, Ching-Shya
Ou Yang, Chih-Ming
Chou, Yenn-Hwei
Liao, Chao-Sheng
Lee, Chung-Wei
Lee, Chin-Cheng
author_facet Yong, Ching-Shya
Ou Yang, Chih-Ming
Chou, Yenn-Hwei
Liao, Chao-Sheng
Lee, Chung-Wei
Lee, Chin-Cheng
author_sort Yong, Ching-Shya
collection PubMed
description BACKGROUND: To correlate CD44/CD24 expression with gastric cancer recurrence and prognosis. Gastric cancer is the second leading cause of cancer mortality due to the high recurrence rate, of which the molecular signature has not yet been identified. METHODS: We retrospectively reviewed the hospital records of patients with gastric cancer. Among 500 patients receiving curative resection, 95 patients had recurrence. Twenty patients from the recurrence group (95 patients) and 20 patients from the non-recurrence group (405 patients) were randomly selected and identified as “study” and “control” groups, respectively. We reviewed patients’ histological study of CD44/CD24 expression by performing immunohistochemistry and recurrence rate. RESULTS: Study group had higher TNM stage (III-IV) than control group (80% vs. 25%, P = 0.001). Proportion of lymph node metastasis was significantly higher in study group than that in control group (90% vs. 45%, P = 0.002), and proportion of patients with 5 or more metastatic lymph nodes was also significantly higher in study group than in control group (45% vs. 15%, P = 0.007). Univariate analysis revealed no difference in risk of gastric cancer recurrence between CD44+ and CD44- patients (OR = 1.00, 95% CI: 0.29-3.45, P =1.000). CD24+ patients showed no greater significance of gastric cancer recurrence than CD24- patients (OR = 1.86, 95% CI: 0.52-6.61, P = 0.339). After adjusting for other risk factors, the association of CD44 expression (aOR = 0.66, 95% CI: 0.10-4.26, P = 0.658), CD24 expression (aOR = 0.09, 95% CI: 0.01-1.35, P = 0.081) or combined (CD44/CD24) with gastric cancer recurrence were not significant. CONCLUSION: Neither individual expression of CD24 or CD44, nor combined expression of CD44/CD24 was associated with recurrence of gastric carcinoma.
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spelling pubmed-34444082012-09-18 CD44/CD24 Expression in recurrent gastric cancer: a retrospective analysis Yong, Ching-Shya Ou Yang, Chih-Ming Chou, Yenn-Hwei Liao, Chao-Sheng Lee, Chung-Wei Lee, Chin-Cheng BMC Gastroenterol Research Article BACKGROUND: To correlate CD44/CD24 expression with gastric cancer recurrence and prognosis. Gastric cancer is the second leading cause of cancer mortality due to the high recurrence rate, of which the molecular signature has not yet been identified. METHODS: We retrospectively reviewed the hospital records of patients with gastric cancer. Among 500 patients receiving curative resection, 95 patients had recurrence. Twenty patients from the recurrence group (95 patients) and 20 patients from the non-recurrence group (405 patients) were randomly selected and identified as “study” and “control” groups, respectively. We reviewed patients’ histological study of CD44/CD24 expression by performing immunohistochemistry and recurrence rate. RESULTS: Study group had higher TNM stage (III-IV) than control group (80% vs. 25%, P = 0.001). Proportion of lymph node metastasis was significantly higher in study group than that in control group (90% vs. 45%, P = 0.002), and proportion of patients with 5 or more metastatic lymph nodes was also significantly higher in study group than in control group (45% vs. 15%, P = 0.007). Univariate analysis revealed no difference in risk of gastric cancer recurrence between CD44+ and CD44- patients (OR = 1.00, 95% CI: 0.29-3.45, P =1.000). CD24+ patients showed no greater significance of gastric cancer recurrence than CD24- patients (OR = 1.86, 95% CI: 0.52-6.61, P = 0.339). After adjusting for other risk factors, the association of CD44 expression (aOR = 0.66, 95% CI: 0.10-4.26, P = 0.658), CD24 expression (aOR = 0.09, 95% CI: 0.01-1.35, P = 0.081) or combined (CD44/CD24) with gastric cancer recurrence were not significant. CONCLUSION: Neither individual expression of CD24 or CD44, nor combined expression of CD44/CD24 was associated with recurrence of gastric carcinoma. BioMed Central 2012-07-28 /pmc/articles/PMC3444408/ /pubmed/22839505 http://dx.doi.org/10.1186/1471-230X-12-95 Text en Copyright ©2012 Yong 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
Yong, Ching-Shya
Ou Yang, Chih-Ming
Chou, Yenn-Hwei
Liao, Chao-Sheng
Lee, Chung-Wei
Lee, Chin-Cheng
CD44/CD24 Expression in recurrent gastric cancer: a retrospective analysis
title CD44/CD24 Expression in recurrent gastric cancer: a retrospective analysis
title_full CD44/CD24 Expression in recurrent gastric cancer: a retrospective analysis
title_fullStr CD44/CD24 Expression in recurrent gastric cancer: a retrospective analysis
title_full_unstemmed CD44/CD24 Expression in recurrent gastric cancer: a retrospective analysis
title_short CD44/CD24 Expression in recurrent gastric cancer: a retrospective analysis
title_sort cd44/cd24 expression in recurrent gastric cancer: a retrospective analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3444408/
https://www.ncbi.nlm.nih.gov/pubmed/22839505
http://dx.doi.org/10.1186/1471-230X-12-95
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