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Clinical Significance of Frizzled Homolog 3 Protein in Colorectal Cancer Patients

Frizzled homolog 3 receptor was up-regulated in several gastrointestinal cancers such as esophageal and gastric cancers. Moreover, frizzled homolog 3 has recently reported to be expressed in colorectal adenoma specimens. In the present study, we investigated the clinical significance of frizzled hom...

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Autores principales: Wong, Sze Chuen Cesar, He, Catherine Wan, Chan, Charles Ming Lok, Chan, Amanda Kit Ching, Wong, Heong Ting, Cheung, Moon Tong, Luk, Lewis Lai Yin, Au, Thomas Chi Chuen, Chiu, Man Kin, Ma, Brigette Buig Yue, Chan, Anthony Tak Cheung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821856/
https://www.ncbi.nlm.nih.gov/pubmed/24255701
http://dx.doi.org/10.1371/journal.pone.0079481
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author Wong, Sze Chuen Cesar
He, Catherine Wan
Chan, Charles Ming Lok
Chan, Amanda Kit Ching
Wong, Heong Ting
Cheung, Moon Tong
Luk, Lewis Lai Yin
Au, Thomas Chi Chuen
Chiu, Man Kin
Ma, Brigette Buig Yue
Chan, Anthony Tak Cheung
author_facet Wong, Sze Chuen Cesar
He, Catherine Wan
Chan, Charles Ming Lok
Chan, Amanda Kit Ching
Wong, Heong Ting
Cheung, Moon Tong
Luk, Lewis Lai Yin
Au, Thomas Chi Chuen
Chiu, Man Kin
Ma, Brigette Buig Yue
Chan, Anthony Tak Cheung
author_sort Wong, Sze Chuen Cesar
collection PubMed
description Frizzled homolog 3 receptor was up-regulated in several gastrointestinal cancers such as esophageal and gastric cancers. Moreover, frizzled homolog 3 has recently reported to be expressed in colorectal adenoma specimens. In the present study, we investigated the clinical significance of frizzled homolog 3 protein in colorectal cancer patients. Using immunocytochemical staining, frizzled homolog 3 expression was examined in 186 colorectal cancer specimens, 79 colorectal adenoma specimens, 133 colorectal polyp specimens, 127 colorectal cancer specimens with lymph node and/or distant metastasis, 310 specimens of various non-colorectal cancer metastatic carcinomas and 40 specimens with simultaneous occurrence of colorectal cancer, colorectal adenoma and colorectal polyp. Statistical analysis was used to correlate frizzled homolog 3 protein expression to the clinicohistopathological factors, recurrence/metastasis and survival after follow-up for 42 months in colorectal cancer patients. Frizzled homolog 3 protein was expressed in 100% colorectal cancer specimens, 89% colorectal adenoma specimens, 75% colorectal polyp specimens and 69% normal colorectal epithelial tissues. Moreover, frizzled homolog 3 immunocytochemical scores were highly correlated with colorectal cancer progression. Furthermore, frizzled homolog 3 was expressed in a comparatively lower percentage of metastatic hepatocellular carcinoma and metastatic renal clear cell carcinoma with focal and very weak staining than other metastatic tumor types. On the other hand, the frizzled homolog 3 immunocytochemical scores of colorectal adenomas with synchronous colorectal carcinomas were significantly higher than those of pure colorectal adenomas. Statistical analysis showed that frizzled homolog 3 immunocytochemical scores were associated with Dukes stage and lymph node status. Finally, stratified groups of colorectal cancer patients had significant differences in their recurrence/metastasis and survival. In conclusion, the present large-scale study has clearly showed that frizzled homolog 3 protein can generate clinically important information for colorectal cancer patients.
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spelling pubmed-38218562013-11-19 Clinical Significance of Frizzled Homolog 3 Protein in Colorectal Cancer Patients Wong, Sze Chuen Cesar He, Catherine Wan Chan, Charles Ming Lok Chan, Amanda Kit Ching Wong, Heong Ting Cheung, Moon Tong Luk, Lewis Lai Yin Au, Thomas Chi Chuen Chiu, Man Kin Ma, Brigette Buig Yue Chan, Anthony Tak Cheung PLoS One Research Article Frizzled homolog 3 receptor was up-regulated in several gastrointestinal cancers such as esophageal and gastric cancers. Moreover, frizzled homolog 3 has recently reported to be expressed in colorectal adenoma specimens. In the present study, we investigated the clinical significance of frizzled homolog 3 protein in colorectal cancer patients. Using immunocytochemical staining, frizzled homolog 3 expression was examined in 186 colorectal cancer specimens, 79 colorectal adenoma specimens, 133 colorectal polyp specimens, 127 colorectal cancer specimens with lymph node and/or distant metastasis, 310 specimens of various non-colorectal cancer metastatic carcinomas and 40 specimens with simultaneous occurrence of colorectal cancer, colorectal adenoma and colorectal polyp. Statistical analysis was used to correlate frizzled homolog 3 protein expression to the clinicohistopathological factors, recurrence/metastasis and survival after follow-up for 42 months in colorectal cancer patients. Frizzled homolog 3 protein was expressed in 100% colorectal cancer specimens, 89% colorectal adenoma specimens, 75% colorectal polyp specimens and 69% normal colorectal epithelial tissues. Moreover, frizzled homolog 3 immunocytochemical scores were highly correlated with colorectal cancer progression. Furthermore, frizzled homolog 3 was expressed in a comparatively lower percentage of metastatic hepatocellular carcinoma and metastatic renal clear cell carcinoma with focal and very weak staining than other metastatic tumor types. On the other hand, the frizzled homolog 3 immunocytochemical scores of colorectal adenomas with synchronous colorectal carcinomas were significantly higher than those of pure colorectal adenomas. Statistical analysis showed that frizzled homolog 3 immunocytochemical scores were associated with Dukes stage and lymph node status. Finally, stratified groups of colorectal cancer patients had significant differences in their recurrence/metastasis and survival. In conclusion, the present large-scale study has clearly showed that frizzled homolog 3 protein can generate clinically important information for colorectal cancer patients. Public Library of Science 2013-11-08 /pmc/articles/PMC3821856/ /pubmed/24255701 http://dx.doi.org/10.1371/journal.pone.0079481 Text en © 2013 Wong 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
Wong, Sze Chuen Cesar
He, Catherine Wan
Chan, Charles Ming Lok
Chan, Amanda Kit Ching
Wong, Heong Ting
Cheung, Moon Tong
Luk, Lewis Lai Yin
Au, Thomas Chi Chuen
Chiu, Man Kin
Ma, Brigette Buig Yue
Chan, Anthony Tak Cheung
Clinical Significance of Frizzled Homolog 3 Protein in Colorectal Cancer Patients
title Clinical Significance of Frizzled Homolog 3 Protein in Colorectal Cancer Patients
title_full Clinical Significance of Frizzled Homolog 3 Protein in Colorectal Cancer Patients
title_fullStr Clinical Significance of Frizzled Homolog 3 Protein in Colorectal Cancer Patients
title_full_unstemmed Clinical Significance of Frizzled Homolog 3 Protein in Colorectal Cancer Patients
title_short Clinical Significance of Frizzled Homolog 3 Protein in Colorectal Cancer Patients
title_sort clinical significance of frizzled homolog 3 protein in colorectal cancer patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821856/
https://www.ncbi.nlm.nih.gov/pubmed/24255701
http://dx.doi.org/10.1371/journal.pone.0079481
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