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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Cancerarrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Cancer
Article . 2003 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
Cancer
Article . 2003
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Clinical significance of vascular endothelial growth factor C and vascular endothelial growth factor receptor 3 in patients with nonsmall cell lung carcinoma

Authors: Mitsuyuki, Arinaga; Tsuyoshi, Noguchi; Shinsuke, Takeno; Masao, Chujo; Takashi, Miura; Yuzo, Uchida;

Clinical significance of vascular endothelial growth factor C and vascular endothelial growth factor receptor 3 in patients with nonsmall cell lung carcinoma

Abstract

AbstractBACKGROUNDVascular endothelial growth factor C (VEGF‐C) plays an important role in lymphangiogenesis and activates VEGF receptor 3 (VEGFR‐3). By contrast, lymphatic spread is an important prognostic factor in patients with nonsmall cell lung carcinoma (NSCLC). The objective of the current study was to determine whether the expression of VEGF‐C and VEGFR‐3 correlates with clinicopathologic factors and prognosis in patients with primary NSCLC.METHODSThe authors conducted a retrospective review of 180 consecutive patients who underwent complete resection for NSCLC and who did not receive any chemotherapy or radiotherapy prior to surgery. Immunohistochemical staining for VEGF‐C and VEGFR‐3 was performed. The clinicopathologic implications of VEGF‐C and VEGFR‐3 expression were analyzed statistically.RESULTSOf 180 patients with NSCLC, 137 patients (76.1%) were positive for VEGF‐C, and 40 patients (22.2%) were positive for VEGFR‐3. VEGF‐C expression was observed frequently in patients with adenocarcinoma (P = 0.026). For VEGFR‐3 expression, significant correlations were demonstrated with age (P = 0.02), gender (P = 0.008), and histologic differentiation in patients with squamous cell carcinoma (P = 0.03). Patients who had positive staining for VEGF‐C showed significantly less favorable survival rates compared with patients who had negative staining for VEGF‐C (P = 0.003). The survival rates of patients who had positive staining for VEGFR‐3 also were significantly lower compared with patients who had negative staining for VEGFR‐3 (P < 0.001). Patients who had positive staining for both VEGF‐C and VEGFR‐3 exhibited the most unfavorable prognoses. Univariate analysis revealed the following prognostic factors: gender (P = 0.03), tumor status (T1,T2 vs. T3; P < 0.01), lymph node status (negative vs. positive; P < 0.01), tumor size (≤ 35 mm vs. > 35 mm; P < 0.01), disease stage (Stage I vs. Stages II and III; P < 0.01), VEGF‐C expression (negative vs. positive; P < 0.01), VEGFR‐3 expression (negative vs. positive; P < 0.01) and combined VEGF‐C and/or VEGFR‐3 expression (both positive vs. VEGF‐C or VEGFR‐3 positive; P < 0.01). Multivariate analysis demonstrated that VEGFR‐3 expression was the only independent negative prognostic factor (P < 0.01).CONCLUSIONSVEGF‐C and VEGFR‐3 expression may be indicative of survival rates for patients with NSCLC. Cancer 2003;97:457–64. © 2003 American Cancer Society.DOI 10.1002/cncr.11073

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Keywords

Adult, Aged, 80 and over, Male, Lung Neoplasms, Vascular Endothelial Growth Factor C, Endothelial Growth Factors, Middle Aged, Prognosis, Vascular Endothelial Growth Factor Receptor-3, Immunohistochemistry, Survival Analysis, Carcinoma, Non-Small-Cell Lung, Multivariate Analysis, Humans, Female, Aged, Retrospective Studies

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    selected citations
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    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    153
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 1%
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
153
Top 10%
Top 10%
Top 1%
Related to Research communities
Cancer Research
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