Evaluation of angiogenesis with the expression of VEGF and CD34 in human non-small cell lung cancer
- Autores
- Inda, Ana María; Andrini, L.; García, Marcela Nilda; García, Adriana Laura; Fernandez Blanco, Ayelen; Furnus, Cecilia Cristina; Galletti, S.M.; Prat, G.D.; Errecalde, Ana Lia
- Año de publicación
- 2007
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Angiogenesis is an essential process in the progression of malignant tumors and the most potent angiogenic factor is the vascular endothelial growth factor (VEGF). On the other hand, the CD34 is an endothelial antigen that has been used to highlight the microvasculature vessel density (MVD) as a direct marker of the degree of neoangiogenesis. In the present study we report the VEGF expression and its relationship with MVD, measured by CD34, in two lineages of non-small cell lung cancer (NSCL): low differentiated adenocarcinomas and epidermoid carcinomas, in order to consider the possibility of using the correlation between both antibodies as a prognostic factor. Tumor sections were stained by immunohistochemistry for CD34 and VEGF. The results showed that the mean value of VEGF for adenocarcinoma was significantly higher than the one for epidermoid carcinoma (p < 0.001). However, the mean of MVD did not show significant differences between both types of tumors. The conventional factors taken into consideration (age over 60, sex, and presence of lymph nodes) was not significantly related to the angiogenic factors examined. In conclusion, we could affirm that CD34 is a better prognostic marker of neoangiogenesis in NSCLC, because both types of tumors have the same clinical prognosis, and so we expected the same behaviour from both markers.
Fil: Inda, Ana María. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina
Fil: Andrini, L.. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina
Fil: García, Marcela Nilda. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina
Fil: García, Adriana Laura. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina
Fil: Fernandez Blanco, Ayelen. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina
Fil: Furnus, Cecilia Cristina. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico CONICET- La Plata. Instituto de Genética Veterinaria "Ing. Fernando Noel Dulout". Universidad Nacional de La Plata. Facultad de Ciencias Veterinarias. Instituto de Genética Veterinaria; Argentina
Fil: Galletti, S.M.. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina
Fil: Prat, G.D.. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; Argentina
Fil: Errecalde, Ana Lia. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina - Materia
-
LUNG CANCER
VEGF
CD34
ANGIOGENESIS
EPIDERMOID CARCINOMA
ADENOCARCINOMA - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/83597
Ver los metadatos del registro completo
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Evaluation of angiogenesis with the expression of VEGF and CD34 in human non-small cell lung cancerInda, Ana MaríaAndrini, L.García, Marcela NildaGarcía, Adriana LauraFernandez Blanco, AyelenFurnus, Cecilia CristinaGalletti, S.M.Prat, G.D.Errecalde, Ana LiaLUNG CANCERVEGFCD34ANGIOGENESISEPIDERMOID CARCINOMAADENOCARCINOMAhttps://purl.org/becyt/ford/3.5https://purl.org/becyt/ford/3Angiogenesis is an essential process in the progression of malignant tumors and the most potent angiogenic factor is the vascular endothelial growth factor (VEGF). On the other hand, the CD34 is an endothelial antigen that has been used to highlight the microvasculature vessel density (MVD) as a direct marker of the degree of neoangiogenesis. In the present study we report the VEGF expression and its relationship with MVD, measured by CD34, in two lineages of non-small cell lung cancer (NSCL): low differentiated adenocarcinomas and epidermoid carcinomas, in order to consider the possibility of using the correlation between both antibodies as a prognostic factor. Tumor sections were stained by immunohistochemistry for CD34 and VEGF. The results showed that the mean value of VEGF for adenocarcinoma was significantly higher than the one for epidermoid carcinoma (p < 0.001). However, the mean of MVD did not show significant differences between both types of tumors. The conventional factors taken into consideration (age over 60, sex, and presence of lymph nodes) was not significantly related to the angiogenic factors examined. In conclusion, we could affirm that CD34 is a better prognostic marker of neoangiogenesis in NSCLC, because both types of tumors have the same clinical prognosis, and so we expected the same behaviour from both markers.Fil: Inda, Ana María. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; ArgentinaFil: Andrini, L.. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; ArgentinaFil: García, Marcela Nilda. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; ArgentinaFil: García, Adriana Laura. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; ArgentinaFil: Fernandez Blanco, Ayelen. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; ArgentinaFil: Furnus, Cecilia Cristina. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico CONICET- La Plata. Instituto de Genética Veterinaria "Ing. Fernando Noel Dulout". Universidad Nacional de La Plata. Facultad de Ciencias Veterinarias. Instituto de Genética Veterinaria; ArgentinaFil: Galletti, S.M.. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; ArgentinaFil: Prat, G.D.. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; ArgentinaFil: Errecalde, Ana Lia. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; ArgentinaAmerican Association for Cancer Research2007-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/83597Inda, Ana María; Andrini, L.; García, Marcela Nilda; García, Adriana Laura; Fernandez Blanco, Ayelen; et al.; Evaluation of angiogenesis with the expression of VEGF and CD34 in human non-small cell lung cancer; American Association for Cancer Research; Journal of Experimental & Clinical Cancer Research; 26; 3; 9-2007; 375-3780392-9078CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://www.ncbi.nlm.nih.gov/pubmed/17987799info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:21:02Zoai:ri.conicet.gov.ar:11336/83597instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-15 14:21:03.137CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Evaluation of angiogenesis with the expression of VEGF and CD34 in human non-small cell lung cancer |
| title |
Evaluation of angiogenesis with the expression of VEGF and CD34 in human non-small cell lung cancer |
| spellingShingle |
Evaluation of angiogenesis with the expression of VEGF and CD34 in human non-small cell lung cancer Inda, Ana María LUNG CANCER VEGF CD34 ANGIOGENESIS EPIDERMOID CARCINOMA ADENOCARCINOMA |
| title_short |
Evaluation of angiogenesis with the expression of VEGF and CD34 in human non-small cell lung cancer |
| title_full |
Evaluation of angiogenesis with the expression of VEGF and CD34 in human non-small cell lung cancer |
| title_fullStr |
Evaluation of angiogenesis with the expression of VEGF and CD34 in human non-small cell lung cancer |
| title_full_unstemmed |
Evaluation of angiogenesis with the expression of VEGF and CD34 in human non-small cell lung cancer |
| title_sort |
Evaluation of angiogenesis with the expression of VEGF and CD34 in human non-small cell lung cancer |
| dc.creator.none.fl_str_mv |
Inda, Ana María Andrini, L. García, Marcela Nilda García, Adriana Laura Fernandez Blanco, Ayelen Furnus, Cecilia Cristina Galletti, S.M. Prat, G.D. Errecalde, Ana Lia |
| author |
Inda, Ana María |
| author_facet |
Inda, Ana María Andrini, L. García, Marcela Nilda García, Adriana Laura Fernandez Blanco, Ayelen Furnus, Cecilia Cristina Galletti, S.M. Prat, G.D. Errecalde, Ana Lia |
| author_role |
author |
| author2 |
Andrini, L. García, Marcela Nilda García, Adriana Laura Fernandez Blanco, Ayelen Furnus, Cecilia Cristina Galletti, S.M. Prat, G.D. Errecalde, Ana Lia |
| author2_role |
author author author author author author author author |
| dc.subject.none.fl_str_mv |
LUNG CANCER VEGF CD34 ANGIOGENESIS EPIDERMOID CARCINOMA ADENOCARCINOMA |
| topic |
LUNG CANCER VEGF CD34 ANGIOGENESIS EPIDERMOID CARCINOMA ADENOCARCINOMA |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.5 https://purl.org/becyt/ford/3 |
| dc.description.none.fl_txt_mv |
Angiogenesis is an essential process in the progression of malignant tumors and the most potent angiogenic factor is the vascular endothelial growth factor (VEGF). On the other hand, the CD34 is an endothelial antigen that has been used to highlight the microvasculature vessel density (MVD) as a direct marker of the degree of neoangiogenesis. In the present study we report the VEGF expression and its relationship with MVD, measured by CD34, in two lineages of non-small cell lung cancer (NSCL): low differentiated adenocarcinomas and epidermoid carcinomas, in order to consider the possibility of using the correlation between both antibodies as a prognostic factor. Tumor sections were stained by immunohistochemistry for CD34 and VEGF. The results showed that the mean value of VEGF for adenocarcinoma was significantly higher than the one for epidermoid carcinoma (p < 0.001). However, the mean of MVD did not show significant differences between both types of tumors. The conventional factors taken into consideration (age over 60, sex, and presence of lymph nodes) was not significantly related to the angiogenic factors examined. In conclusion, we could affirm that CD34 is a better prognostic marker of neoangiogenesis in NSCLC, because both types of tumors have the same clinical prognosis, and so we expected the same behaviour from both markers. Fil: Inda, Ana María. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina Fil: Andrini, L.. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina Fil: García, Marcela Nilda. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina Fil: García, Adriana Laura. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina Fil: Fernandez Blanco, Ayelen. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina Fil: Furnus, Cecilia Cristina. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico CONICET- La Plata. Instituto de Genética Veterinaria "Ing. Fernando Noel Dulout". Universidad Nacional de La Plata. Facultad de Ciencias Veterinarias. Instituto de Genética Veterinaria; Argentina Fil: Galletti, S.M.. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina Fil: Prat, G.D.. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; Argentina Fil: Errecalde, Ana Lia. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Departamento de Ciencias Morfológicas. Cátedra de Citología y Embriología A; Argentina |
| description |
Angiogenesis is an essential process in the progression of malignant tumors and the most potent angiogenic factor is the vascular endothelial growth factor (VEGF). On the other hand, the CD34 is an endothelial antigen that has been used to highlight the microvasculature vessel density (MVD) as a direct marker of the degree of neoangiogenesis. In the present study we report the VEGF expression and its relationship with MVD, measured by CD34, in two lineages of non-small cell lung cancer (NSCL): low differentiated adenocarcinomas and epidermoid carcinomas, in order to consider the possibility of using the correlation between both antibodies as a prognostic factor. Tumor sections were stained by immunohistochemistry for CD34 and VEGF. The results showed that the mean value of VEGF for adenocarcinoma was significantly higher than the one for epidermoid carcinoma (p < 0.001). However, the mean of MVD did not show significant differences between both types of tumors. The conventional factors taken into consideration (age over 60, sex, and presence of lymph nodes) was not significantly related to the angiogenic factors examined. In conclusion, we could affirm that CD34 is a better prognostic marker of neoangiogenesis in NSCLC, because both types of tumors have the same clinical prognosis, and so we expected the same behaviour from both markers. |
| publishDate |
2007 |
| dc.date.none.fl_str_mv |
2007-09 |
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article |
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publishedVersion |
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http://hdl.handle.net/11336/83597 Inda, Ana María; Andrini, L.; García, Marcela Nilda; García, Adriana Laura; Fernandez Blanco, Ayelen; et al.; Evaluation of angiogenesis with the expression of VEGF and CD34 in human non-small cell lung cancer; American Association for Cancer Research; Journal of Experimental & Clinical Cancer Research; 26; 3; 9-2007; 375-378 0392-9078 CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/83597 |
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Inda, Ana María; Andrini, L.; García, Marcela Nilda; García, Adriana Laura; Fernandez Blanco, Ayelen; et al.; Evaluation of angiogenesis with the expression of VEGF and CD34 in human non-small cell lung cancer; American Association for Cancer Research; Journal of Experimental & Clinical Cancer Research; 26; 3; 9-2007; 375-378 0392-9078 CONICET Digital CONICET |
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eng |
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American Association for Cancer Research |
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American Association for Cancer Research |
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