PMID- 15856293 OWN - NLM STAT- MEDLINE DCOM- 20050927 LR - 20181113 IS - 0945-6317 (Print) IS - 0945-6317 (Linking) VI - 446 IP - 6 DP - 2005 Jun TI - Vascular endothelial growth factor in salivary pleomorphic adenomas: one of the reasons for their poorly vascularized stroma. PG - 653-62 AB - To better understand the poorly vascularized background of the stroma of pleomorphic adenomas, we attempted to determine the expression of molecules related to blood vessels and hypoxic conditions in pleomorphic adenoma. Surgical specimens and tumor cells in primary culture of salivary pleomorphic adenomas were used for immunohistochemistry for CD31, vascular endothelial growth factor (VEGF) and its receptors Flk-1 and Flt-1, as well as for hypoxia markers, such as hypoxia-inducible factor-1alpha (HIF-1alpha) and lactate dehydrogenase-1 (LDH). At the same time, alternative splicing modes of the VEGF gene and expression levels of the HIF-1alpha gene were analyzed in surgical specimens by means of reverse-transcription polymerase chain reaction (RT-PCR) and direct sequencing of the PCR products. In addition to co-immunolocalization with CD31+ vascular endothelial cells, VEGF and its receptors were demonstrated in normal duct epithelial and myoepithelial cells as well as in tumor cells in ductal structures and in myxochondroid stromata. Immunolocalizations for HIF-1alpha and LDH were confirmed in the VEGF-positive area. Immunofluorescence signals for VEGF and others were confirmed in pleomorphic adenoma cells in culture. RT-PCR results showed that there were at least four splicing modes of the VEGF gene, among which VEGF(121) was most enhanced, and higher HIF-1alpha levels in pleomorphic adenomas. The results suggest that pleomorphic adenoma cells produce VEGF in several functional forms for their own proliferation or differentiation, and that the VEGF expression is controlled by hypoxic circumstances of poorly vascularized pleomorphic adenomas. FAU - Swelam, Wael AU - Swelam W AD - Department of Tissue Regeneration and Reconstruction, Division of Oral Pathology, Niigata University Graduate School of Medical and Dental Sciences, 2-5274 Gakkocho-dori, Niigata 951-8514, Japan. FAU - Ida-Yonemochi, Hiroko AU - Ida-Yonemochi H FAU - Maruyama, Satoshi AU - Maruyama S FAU - Ohshiro, Kazufumi AU - Ohshiro K FAU - Cheng, Jun AU - Cheng J FAU - Saku, Takashi AU - Saku T LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20050423 PL - Germany TA - Virchows Arch JT - Virchows Archiv : an international journal of pathology JID - 9423843 RN - 0 (Biomarkers, Tumor) RN - 0 (HIF1A protein, human) RN - 0 (Hypoxia-Inducible Factor 1, alpha Subunit) RN - 0 (Platelet Endothelial Cell Adhesion Molecule-1) RN - 0 (Proteins) RN - 0 (RNA, Messenger) RN - 0 (Receptors, Fibroblast Growth Factor) RN - 0 (Transcription Factors) RN - 0 (Vascular Endothelial Growth Factor A) RN - EC 2.7.10.1 (FGFR1 protein, human) RN - EC 2.7.10.1 (FLT1 protein, human) RN - EC 2.7.10.1 (Receptor Protein-Tyrosine Kinases) RN - EC 2.7.10.1 (Receptor, Fibroblast Growth Factor, Type 1) RN - EC 2.7.10.1 (Vascular Endothelial Growth Factor Receptor-1) SB - IM MH - Adenoma, Pleomorphic/*blood supply/metabolism MH - Alternative Splicing MH - Biomarkers, Tumor/analysis MH - Fluorescent Antibody Technique MH - Humans MH - Hypoxia/metabolism/*physiopathology MH - Hypoxia-Inducible Factor 1, alpha Subunit MH - Image Processing, Computer-Assisted MH - Immunohistochemistry MH - Platelet Endothelial Cell Adhesion Molecule-1/metabolism MH - Proteins/metabolism MH - RNA, Messenger/analysis MH - Receptor Protein-Tyrosine Kinases/metabolism MH - Receptor, Fibroblast Growth Factor, Type 1 MH - Receptors, Fibroblast Growth Factor/metabolism MH - Reverse Transcriptase Polymerase Chain Reaction MH - Salivary Gland Neoplasms/*blood supply/metabolism MH - Transcription Factors/metabolism MH - Vascular Endothelial Growth Factor A/*genetics/*metabolism MH - Vascular Endothelial Growth Factor Receptor-1 EDAT- 2005/04/28 09:00 MHDA- 2005/09/28 09:00 CRDT- 2005/04/28 09:00 PHST- 2004/11/11 00:00 [received] PHST- 2005/01/24 00:00 [accepted] PHST- 2005/04/28 09:00 [pubmed] PHST- 2005/09/28 09:00 [medline] PHST- 2005/04/28 09:00 [entrez] AID - 10.1007/s00428-005-1219-1 [doi] PST - ppublish SO - Virchows Arch. 2005 Jun;446(6):653-62. doi: 10.1007/s00428-005-1219-1. Epub 2005 Apr 23.