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The Upregulated Expression of Vascular Endothelial Growth Factor in Surgically Treated Patients with Recurrent/radioresistant Cervical Cancer of the Uterus

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Journal Oncol Lett
Specialty Oncology
Date 2018 Jun 22
PMID 29928441
Citations 11
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Abstract

Vascular endothelial growth factor (VEGF) inhibitors have been utilized for the treatment against advanced or recurrent cervical carcinoma as a novel therapeutic modality. However, the expression level of VEGF in post-radiotherapy relapsed/persistent cervical cancer remains to be elucidated. The aim of the present study was to investigate the expression of VEGF and associated molecules using tumor samples from patients with post-radiotherapy relapsed/persistent cervical cancer. From a database of 826 patients who were treated at our institution between 2003 and 2015, eight patients with post-radiotherapy relapsed/persistent cervical cancer were identified, and 20 patients who underwent initial surgery alone were used as a control. Using samples from these patients, the expression levels of VEGF-A, VEGF receptor-1 (VEGFR-1) and hypoxia inducible factor-1α (HIF-1α) were immunohistochemically categorized as negative or weakly, moderately, or strongly positive according to the size of the staining area, and intensity. In carcinoma cells, the expression levels of VEGF-A, VEGFR-1 and HIF-1α were significantly higher in post-radiotherapy relapsed/persistent cervical cancer compared with control patients (P=0.0003, 0.0003, and 0.0001, respectively). In stroma cells, similar tendencies with statistical significance were observed (P=0.0014 and P<0.0001, respectively). In addition, the expression levels of VEGF-A and VEGFR-1 in carcinoma cells were significantly correlated with each other (P<0.0001). A significantly higher expression of VEGF was identified in post-radiotherapy relapsed/persistent cervical cancer compared with typical specimens from cervical cancer. The findings provide a novel insight into the clinical treatment for recurrent/persistent cervical cancer using a VEGF antagonist.

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References
1.
Schefter T, Winter K, Kwon J, Stuhr K, Balaraj K, Yaremko B . RTOG 0417: efficacy of bevacizumab in combination with definitive radiation therapy and cisplatin chemotherapy in untreated patients with locally advanced cervical carcinoma. Int J Radiat Oncol Biol Phys. 2013; 88(1):101-5. DOI: 10.1016/j.ijrobp.2013.10.022. View

2.
Iwasaki K, Yabushita H, Ueno T, Wakatsuki A . Role of hypoxia-inducible factor-1α, carbonic anhydrase-IX, glucose transporter-1 and vascular endothelial growth factor associated with lymph node metastasis and recurrence in patients with locally advanced cervical cancer. Oncol Lett. 2015; 10(4):1970-1978. PMC: 4579921. DOI: 10.3892/ol.2015.3524. View

3.
Benedet J, Odicino F, Maisonneuve P, Beller U, Creasman W, Heintz A . Carcinoma of the cervix uteri. Int J Gynaecol Obstet. 2004; 83 Suppl 1:41-78. DOI: 10.1016/s0020-7292(03)90115-9. View

4.
Fu Z, Chen D, Cheng H, Wang F . Hypoxia-inducible factor-1α protects cervical carcinoma cells from apoptosis induced by radiation via modulation of vascular endothelial growth factor and p53 under hypoxia. Med Sci Monit. 2015; 21:318-25. PMC: 4316866. DOI: 10.12659/MSM.893265. View

5.
Jiang B, Agani F, Passaniti A, Semenza G . V-SRC induces expression of hypoxia-inducible factor 1 (HIF-1) and transcription of genes encoding vascular endothelial growth factor and enolase 1: involvement of HIF-1 in tumor progression. Cancer Res. 1997; 57(23):5328-35. View