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Aberrant expression of CD133 in non-small cell lung cancer and its relationship to vasculogenic mimicry
BACKGROUND: To investigate on expressions and clinical significances of CD133 protein and vasculogenic mimicry (VM) in primary non-small cell lung cancer (NSCLC). METHODS: The specimens of NSCLC from 305 Chinese patients with follow-up were analyzed for CD133 protein expression and VM by immunohisto...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518202/ https://www.ncbi.nlm.nih.gov/pubmed/23170850 http://dx.doi.org/10.1186/1471-2407-12-535 |
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author | Wu, Shiwu Yu, Lan Wang, Danna Zhou, Lei Cheng, Zenong Chai, Damin Ma, Li Tao, Yisheng |
author_facet | Wu, Shiwu Yu, Lan Wang, Danna Zhou, Lei Cheng, Zenong Chai, Damin Ma, Li Tao, Yisheng |
author_sort | Wu, Shiwu |
collection | PubMed |
description | BACKGROUND: To investigate on expressions and clinical significances of CD133 protein and vasculogenic mimicry (VM) in primary non-small cell lung cancer (NSCLC). METHODS: The specimens of NSCLC from 305 Chinese patients with follow-up were analyzed for CD133 protein expression and VM by immunohistochemical and histochemical staining. RESULTS: In NSCLC, positive rates of 48.9% and 35.7% were obtained for CD133 and VM, respectively. The VM and expression of CD133 were significantly higher in carcinoma than in normal. There were a positive relationship between the VM and expression of CD133 and the tumor grade, lymph node metastasis and clinical stage (all P<0.05). The overall mean survival time of the patients with CD133 and VM positive expression was lower than that of patients with negative expression. Microvessel density (MVD) was positive corresponded with the grade, lymph node metastasis and clinical stage (all P<0.05). The overall mean survival time of the patients with MVD≥22’s group was shorter than that of patients with MVD<22’s group. Pathological-tumor-node-metastasis (pTNM) stage, positive expression of CD133 and VM, postoperative therapy and MVD were independent prognostic factors of NSCLC (P<0.05). Immunohistochemistry revealed an important intratumoral heterogeneity in all four CD133 expression profiles. CONCLUSIONS: VM, MVD and expression of CD133 are related to differentiation, lymph node metastasis, clinical stage, and prognosis. It is suggested that CD133, VM and MVD should be considered as a potential marker for the prognosis. |
format | Online Article Text |
id | pubmed-3518202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35182022012-12-11 Aberrant expression of CD133 in non-small cell lung cancer and its relationship to vasculogenic mimicry Wu, Shiwu Yu, Lan Wang, Danna Zhou, Lei Cheng, Zenong Chai, Damin Ma, Li Tao, Yisheng BMC Cancer Research Article BACKGROUND: To investigate on expressions and clinical significances of CD133 protein and vasculogenic mimicry (VM) in primary non-small cell lung cancer (NSCLC). METHODS: The specimens of NSCLC from 305 Chinese patients with follow-up were analyzed for CD133 protein expression and VM by immunohistochemical and histochemical staining. RESULTS: In NSCLC, positive rates of 48.9% and 35.7% were obtained for CD133 and VM, respectively. The VM and expression of CD133 were significantly higher in carcinoma than in normal. There were a positive relationship between the VM and expression of CD133 and the tumor grade, lymph node metastasis and clinical stage (all P<0.05). The overall mean survival time of the patients with CD133 and VM positive expression was lower than that of patients with negative expression. Microvessel density (MVD) was positive corresponded with the grade, lymph node metastasis and clinical stage (all P<0.05). The overall mean survival time of the patients with MVD≥22’s group was shorter than that of patients with MVD<22’s group. Pathological-tumor-node-metastasis (pTNM) stage, positive expression of CD133 and VM, postoperative therapy and MVD were independent prognostic factors of NSCLC (P<0.05). Immunohistochemistry revealed an important intratumoral heterogeneity in all four CD133 expression profiles. CONCLUSIONS: VM, MVD and expression of CD133 are related to differentiation, lymph node metastasis, clinical stage, and prognosis. It is suggested that CD133, VM and MVD should be considered as a potential marker for the prognosis. BioMed Central 2012-11-21 /pmc/articles/PMC3518202/ /pubmed/23170850 http://dx.doi.org/10.1186/1471-2407-12-535 Text en Copyright ©2012 Wu 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 Wu, Shiwu Yu, Lan Wang, Danna Zhou, Lei Cheng, Zenong Chai, Damin Ma, Li Tao, Yisheng Aberrant expression of CD133 in non-small cell lung cancer and its relationship to vasculogenic mimicry |
title | Aberrant expression of CD133 in non-small cell lung cancer and its relationship to vasculogenic mimicry |
title_full | Aberrant expression of CD133 in non-small cell lung cancer and its relationship to vasculogenic mimicry |
title_fullStr | Aberrant expression of CD133 in non-small cell lung cancer and its relationship to vasculogenic mimicry |
title_full_unstemmed | Aberrant expression of CD133 in non-small cell lung cancer and its relationship to vasculogenic mimicry |
title_short | Aberrant expression of CD133 in non-small cell lung cancer and its relationship to vasculogenic mimicry |
title_sort | aberrant expression of cd133 in non-small cell lung cancer and its relationship to vasculogenic mimicry |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518202/ https://www.ncbi.nlm.nih.gov/pubmed/23170850 http://dx.doi.org/10.1186/1471-2407-12-535 |
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