期刊论文详细信息
Journal of Experimental & Clinical Cancer Research
Endothelial follicle-stimulating hormone receptor expression in invasive breast cancer and vascular remodeling at tumor periphery
Nicolae Ghinea4  Martine Antoine2  Xavier Sastre-Garau3  Christophe Pichon4  Blaise Robin4  François-Clément Bidard1  Mohammad-Ahsan Siraj4  François Planeix4 
[1] Curie Hospital, Oncology Department, 26 rue d’Ulm, Paris, France;Tenon Hospital, Pathology Department, 4 rue de la Chine, Paris, France;Curie Hospital, Pathology Department, 26 rue d’Ulm, Paris, France;INSERM “Tumoral Angiogenesis” Laboratory, Curie Institute, Research Center, Translational Research Department, 26 rue d’Ulm, Paris, France
关键词: Vascular remodeling;    Triple negative breast cancer;    Progesterone receptor;    Podoplanin;    Lymphangiogenesis;    HER2;    FSHR;    Estrogen receptor;    CD34;    Breast cancer subtype;    Angiogenesis;   
Others  :  1133390
DOI  :  10.1186/s13046-015-0128-7
 received in 2014-12-22, accepted in 2015-01-20,  发布年份 2015
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【 摘 要 】

Background

Follicle-stimulating hormone receptor (FSHR) is expressed on the endothelial surface of blood vessels associated with solid tumor periphery, where angiogenesis is known to occur. The correlation between FSHR expression and formation of new peritumoral vessels has not been previously investigated.

Methods

We used immunohistochemical techniques involving specific antibodies to detect FSHR and the endothelial markers (CD34, VEGFR2, and D2-40) in tissue samples from 83 patients with lymph node-negative, invasive breast cancer representing four main clinical treatment groups: HR+/HER2-, HR+/HER2+, HR-/HER2+ and triple-negative.

Results

The FSHR+ vessels were exclusively located at breast cancer periphery, in a layer that extended 2 mm into and 5 mm outside of the tumor. The percentage of blood vessels expressing FSHR reached a maximum of 100% at the demarcation line between the tumor and the normal tissue. Common among FSHR+ vessels, regardless of breast cancer type, were the high densities of arterioles and venules (6.4 ± 1.4 and 13.9 ± 2.1 vessels/mm2, respectively). These values were 3-fold higher that those noticed for CD34+ arterioles and venules associated with normal breast tissue located at a distance greater than 10 mm outside the tumors. The average density of FSHR+ and CD34+ blood vessels as well as of D2-40+ lymphatic vessels did not differ significantly among breast cancer subgroups. FSHR+ vessels did not express VEGFR2. The endothelial FSHR expression correlated significantly with the peritumoral CD34+ vessels’ density (p < 0.001) and tumor size (p = 0.01).

Conclusion

Endothelial FSHR expression in breast cancer is associated with vascular remodeling at tumor periphery.

【 授权许可】

   
2015 Planeix et al.; licensee BioMed Central.

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