Abstract | OBJECTIVE: METHOD: The expression of CXCR4 in fresh laryngeal squamous carcinoma tissues and adjacent normal tissues from 42 patients were examined by RT-PCR, immunohistochemical staining and Image-pro-plus software. The numbers of regeneration blood vessels in the laryngeal squamous carcinoma was counted by antibody against factor V associated antigen and immunohistochemical analysis. RESULT: The positive expression rate of CXCR4 in tumor samples was significantly higher than that in normal ones (P < 0.01). In tumor samples, the expression of CXCR4 were not associated with age, sex, tumor site and T stage (P > 0.05), while it were higher in tumors of grade III, IV than in grade I, II of pathology classification (P < 0. 01). The expression of CXCR4 were significantly higher in tumors with cervical lymph node metastasis than that in tumor without cervical lymph node metastasis (P < 0.01). The expression of CXCR4 protein and CXCR4 mRNA were at the same level. The expression level of CXCR4 in the laryngeal squamous carcinoma tissue was positively correlated with vascularization. CONCLUSION: The higher expression of CXCR4 may play a key role in the invasion and metastasis of laryngeal squamous carcinoma, and were correlated with micro-vascularization.
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Authors | Chuanming Zheng, Rongming Ge, Minghua Ge, Xicai Sun |
Journal | Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery
(Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi)
Vol. 25
Issue 3
Pg. 123-6
(Feb 2011)
ISSN: 2096-7993 [Print] China |
PMID | 21553525
(Publication Type: English Abstract, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- CXCR4 protein, human
- Receptors, CXCR4
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Carcinoma, Squamous Cell
(blood supply, metabolism, pathology)
- Female
- Humans
- Laryngeal Neoplasms
(blood supply, metabolism, pathology)
- Lymphatic Metastasis
- Microvessels
(pathology)
- Middle Aged
- Neoplasm Staging
- Neovascularization, Pathologic
(pathology)
- Receptors, CXCR4
(metabolism)
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