BMP4, a new prognostic factor for glioma

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WORLD JOURNAL OF SURGICAL ONCOLOGY

RESEARCH

Open Access

BMP4, a new prognostic factor for glioma Qiang Wu1* and Jiarui Yao2

Abstract Background: The expression status of bone morphogenetic protein 4 (BMP4) in gliomas is still unclear by now. We try to investigate the relationship between BMP4 expression and the biological behavior of gliomas in order to lay a foundation for the management of these tumors. Methods: A total of 630 patients with glioma were enrolled in the study from January 2002 to January 2008. The expression status of BMP4 in gliomas was evaluated by RT-PCR and immunohistochemistry. The relationships between BMP4 expression and clinicopathological parameters and between BMP4 expression and prognosis were also studied. Results: The expression of BMP4 in tumor tissues was significantly lower than that in the paracancer tissues at both mRNA and protein levels (P = 0.01 and 0.001, respectively). Univariate analysis showed that BMP4 expression was closely related to extent of resection, Ki-67 expression, and the WHO grade (P = 0.001, 0.001, and 0.001, respectively), but it was not related to age, sex, or the Karnofsky Performance Status (KPS) score (P = 0.099, 0.472, and 0.201, respectively). Finally, Ki-67 expression and the WHO grade were found to be related to BMP4 expression using logistic regression (P = 0.001 and 0.001, respectively). Interestingly, we found that the expression of BMP4 was significantly related to distant glioma metastasis. Cox regression analysis identified the KPS score, extent of resection, Ki-67 expression, WHO grade, and BMP4 expression as independent prognostic factors (P = 0.044, 0.010, 0.002, 0.001, and 0.001, respectively). Conclusions: BMP4 is differentially expressed in glioma patients and is closely related to the biological behavior of gliomas. BMP4 expression was found to be a strong predictor of distant metastasis and postoperative prognosis. Keywords: Glioma, RT-PCR, Immunohistochemistry, BMP4, Survival rate

Background A glioma is a type of tumor that starts in the brain or spine. Gliomas make up approximately 30% of all brain and central nervous system tumors and 80% of all malignant brain tumors [1]. They are fast growing and have a high recurrence rate [2]. The five-year survival rate for patients with glioma is low even with surgery, radiotherapy, chemotherapy, and other forms of treatment [3]. Because of the infiltrative growth of gliomas, it is difficult to resect the whole tumor without causing serious damage to brain function [4]. The use of molecular biology methods to explore the pathogenic basis of gliomas may yield further insight into the treatment of this disease.

* Correspondence: [email protected] 1 Department of Neurology, Xinxiang Central Hospital, 56 Jin Hui Da Street, Henan 453000, China Full list of author information is available at the end of the article

Bone morphogenetic proteins (BMPs) are multifunctional growth factors that belong to the transforming growth factor beta (TGF-β) superfamily [5]. Members of the TGF-β superfamily