Expression of Bone Morphogenetic Protein-7 Significantly Correlates With Non-small Cell Lung Cancer Progression and Prognosis: A Retrospective Cohort Study
Bone morphogenetic protein-7 (BMP-7) is a signaling molecule belonging to the transforming growth factor-β superfamily. Recent studies have demonstrated that BMP-7 is expressed in various human cancers and plays an important role in the progression of their cancers. The purpose of this study was to investigate the clinicopathologic and prognostic impact of BMP-7 expression in clinical samples of non-small cell lung cancer.
This study enrolled 160 patients with non-small cell lung cancer who underwent complete resection. Expression of BMP-7 in cancer tissue was evaluated by immunohistochemistry. Correlations between expression of BMP-7 and clinicopathologic factors and prognosis were analyzed.
In non-small cell lung cancer, BMP-7 expression was identified not only in cell membranes but also in the cytoplasm of cancer cells. Expression of BMP-7 correlated with p-T (P = .047), N factor (P = .013), and p-stage (P = .046). Overall survival rate was significantly lower in the BMP-7-positive group than in the BMP-7-negative group (P = .004). Multivariate analysis indicated that BMP-7 expression was one of the independent prognosis factors of overall survival (P = .021). Furthermore, among patients with postoperative recurrence (n = 58), the BMP-7-positive group (n = 29) had a significantly poorer prognosis than the BMP-7-negative group (n = 29) (P = .012).
Lung cancer has a high incidence and mortality for all cancers worldwide.1 The reasons for the high mortality of non-small cell lung cancer (NSCLC) are that patients are diagnosed in advanced stages and recurrence is common, even among patients who have received curative surgery. Selecting appropriate treatment for patients with NSCLC requires that novel molecular markers for diagnosis and prediction of prognosis be found.
BMPs (bone morphogenetic proteins) are signaling molecules belonging to the transforming growth factor-β superfamily, with more than 30 subtypes in mammals, Drosophila, Xenopus, and sea urchins. The function of BMPs is linked to bone tissue morphogenesis as well as cellular homeostasis and embryonic development.2-5
Expression of bone morphogenetic protein-7 (BMP-7) is highest in the kidney, and it is thought that BMP-7 itself is related to kidney and eye development as well as skeletal patterning.3,6 Recent studies have demonstrated that BMP-7 is also expressed in various human solid cancers and regulates cell proliferation, migration, invasion, and apoptosis.7-9 However, to our knowledge, there have been few reports investigating an association between BMP-7 expression and clinicopathologic factors, including prognosis, in NSCLC. Thus, the purpose of this study was to investigate BMP-7 expression by immunohistochemistry in NSCLC and evaluate the clinical impact of BMP-7-positivity in NSCLC.
Patients and specimens
This retrospective cohort study enrolled 160 patients with NSCLC. All patients had undergone complete resection at Kagoshima University Hospital from January 2001 to December 2007 (Table 1). Patients had undergone lobectomy (n = 154), bi-lobectomy (n = 4), or pneumonectomy (n = 2) with mediastinal lymphadenectomy. In this study, cases receiving neoadjuvant therapy were not included. Of the 160 patients with NSCLC, 102 were men and 58 were women, and the mean age was 69 years (range = 26-84 years). The final pathologic examination disclosed NSCLC stages IA (n = 50), IB (n = 52), IIA (n = 16), IIB (n = 15), and IIIA (n = 27). The patients were histopathologically classified as adenocarcinomas (n = 112), squamous cell carcinomas (n = 40), or “others” (adenosquamous carcinoma, large cell carcinoma, mucoepidermoid carcinoma, pleomorphic carcinoma; n = 8) according to the Association for the Study of Lung Cancer TNM (tumor-node-metastasis) classification, 7th edition.10 Written informed consent was obtained from the patients and the study was approved by the Ethical Committee of Kagoshima University Hospital (registration number 351). This investigation conformed to the principles outlined in the Declaration of Helsinki.
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Immunohistochemistry of BMP-7 in NSCLC
NSCLC specimens were fixed in formalin, embedded in paraffin, and then cut into 3-μm-thick sections and mounted on glass slides for immunohistochemistry. Specimens were then deparaffinized in xylene and dehydrated with a series of graded ethanol. The endogenous peroxidase activity of specimens was blocked by immersing the slides in a 0.3% hydrogen peroxide solution in methanol for 30 minutes at room temperature. After the sections were washed 3 times with phosphate-buffered saline (PBS) for 5 minutes each, they were treated with 1% bovine serum albumin for 30 minutes to block nonspecific reactions at room temperature. The blocked sections were incubated with the mouse monoclonal antibody against human BMP-7 (1:500; R&D Systems, Inc., Minneapolis, MN, USA) and left overnight at 4°C, followed by staining with a streptavidin-biotin peroxidase kit (Vector Laboratories, Inc., Burlingame, CA, USA). The sections were washed in PBS for 5 minutes 3 times and the immune complex was visualized by incubating the sections with diaminobenzidine tetrahydrochloride. The sections were rinsed briefly in water, counterstained with hematoxylin, and mounted. Noncancerous kidney samples were used as positive controls for BMP-7. BMP-7 expression was determined by counting the number of cancer cells in which the cytoplasm was stained with the anti-BMP-7 antibody. Two investigators (MA and MS) independently evaluated BMP-7 expression via immunohistochemistry within each tumor by assessing a total of 1000 cancer cells in 10 selected fields (100 cells/field) using high-power (×200) microscopy. The average labeling index of BMP-7 was assessed according to the proportion of positive cells in each field. The average expression rate of BMP-7 in all cases was 25.3%. BMP-7 expression was graded as the BMP-7-positive group if more than 30% of cancer cells were stained or as the BMP-7-negative group if less than 30% of cancer cells were stained.
Statistical analysis
A statistical analysis of group differences was performed using the chi-square test. Survival was analyzed using the Kaplan-Meier method and evaluated by the log-rank test. The Cox proportional hazard model was used in the multivariate analysis. A P value of <.05 was considered statistically significant.
Bone morphogenetic protein-7 expression in NSCLC and its association with clinicopathologic factors
In NSCLC, BMP-7 expression was identified not only in cell membranes but also in the cytoplasm of cancer cells (Figure 1). According to immunohistochemical evaluation of the samples, the patients were classified into a BMP-7-positive group (n = 68, 43%) and a BMP-7-negative group (n = 92). Table 2 shows the expression of BMP-7 and correlation with clinicopathologic factors. Comparing the BMP-7-positive group with the BMP-7-negative group, BMP-7 expression correlated significantly with several clinicopathologic variables, namely, p-T factor (P = .047), p-N factor (P = .013), and p-stage (P = .046). The BMP-7-positive group tend to be more in men than women (P = .069). The other clinicopathologic factors such as age, tumor size, pleural invasion, pulmonary metastasis, and histology were not correlated with the expression of BMP-7 (P > .05 for all).
Figure 1. Expression of BMP-7 in clinical samples. Immunohistochemical staining of BMP-7 (original magnification, ×400): examples of (A) noncancerous kidney tissue, (B) BMP-7-positive NSCLC, and (C) BMP-7-negative NSCLC. Staining is detected in both cell membranes and the cytoplasm. BMP-7 indicates bone morphogenetic protein-7; NSCLC, non-small cell lung cancer.
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Univariate and multivariate analyses of survival
In term of prognosis of patients, although recurrence-free survival was not correlated with the expression of BMP-7 (P = .273; Figure 2A), the overall survival rate was significantly lower in the BMP-7-positive group than in the BMP-7-negative group (P = .004; Figure 2B). Furthermore, among patients with postoperative recurrence (n = 58), patients with BMP-7-positive (n = 29) had a significantly poorer prognosis than patients with BMP-7-negative (n = 29) (P = .012; Figure 2C).
Figure 2. Postoperative survival curves of patients according to their expression of BMP-7 in NSCLC. Although recurrence-free survival was not correlated with BMP-7 expression (P = .273), (A) overall survival rate was significantly lower in the BMP-7-positive group than in the (B) BMP-7-negative group (P = .004). (C) In the postoperative recurrence cases, BMP-7-positive group was a significantly poorer prognosis than BMP-7-negative group (P = .012). BMP-7 indicates bone morphogenetic protein-7; NSCLC, non-small cell lung cancer.
Table 3 shows the results of univariate and multivariate analyses of factors related to the overall survival. Univariate analysis showed that age (P = .035), tumor size (P < .001), p-T factor (P = .057), p-N factor (P = .003), and BMP-7 expression (P = .004) were significantly related to postoperative survival. Multivariate analysis indicated that BMP-7 expression was one of the independent prognostic factors of overall survival for the patients with NSCLC (P = .021) next to the tumor size (P = .002) and p-N factor (P = .003).
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Recently, BMP-7 expression has been identified, and clinical features of its expression in several human solid cancers such as osteosarcoma, prostate cancer, colorectal cancer, malignant melanoma, breast cancer, esophageal cancer, gastric cancer, and renal cell cancer have been discussed.11-18 In this study, we showed that BMP-7 expression was significantly associated with several clinicopathologic factors such as p-T, N factor, and p-stage. Liu et al19 demonstrated that downregulation of BMP-7 expression significantly inhibited the invasiveness of SPC-A1 cells whereas forced expression of BMP-7 dramatically increased the motility of A549 cells. Furthermore, previous studies have demonstrated that BMP-7 promoted breast cancer cell migration and invasion, prostate cancer cell mobility, and related metastasis in colorectal cancer.7-9 In NSCLC, Yang et al20 reported that restoration of BMP-7 remarkably reversed the tumor suppressive effects of miR-137 on NSCLC tissues. On the contrary, X Ying et al21 reported that BMP-7 suppresses epithelial mesenchymal transition (EMT) of breast cancer cells, which is opposite to this study. It is difficult to prove the contradiction of this result in this study. However, there is no doubt that BMP-7 controls the tumor progression by various ways beyond the specific organ of cancer origin.
In prognosis, Motoyama et al16 reported that overexpression of BMP-7 messenger RNA was significantly associated with poorer overall survival in colorectal cancer. Moreover, BMP-7 expression demonstrated by immunohistochemistry was also significantly associated with poorer survival in malignant melanoma, breast cancer, esophageal cancer, and gastric cancer.11,12,15,17 We showed that BMP-7 expression in NSCLC was an independent prognostic marker in accordance with results for other cancers. Only in renal cell cancer, BMP-7 expression has been significantly associated with better surgical outcome.13 Unlike normal lung tissue, normal kidney cells usually express BMP-7 at high levels, and this difference might result in the variation in prognostic implication for this marker.
An interesting finding of this study was that although recurrence-free survival was not correlated with BMP-7 expression, the overall survival rate was significantly lower in the BMP-7-positive group than in the BMP-7-negative group. According to the subset analysis of patients with postoperative recurrence, the BMP-7-positive group had a significantly poorer prognosis than the BMP-7-negative group. Moreover, as mentioned above, BMP-7 expression was significantly associated with clinical factors such as p-T, N factor, and p-stage. These facts suggest that BMP-7 has a role in the NSCLC progression.
BMPs mediate their effects through activation of type I/II serine/threonine kinase receptors on cell membranes. After BMPs bind these receptors via an autocrine or paracrine route, Smad1/5/8 is induced by phosphorylation and assembled into heteromeric complexes with Smad4 in the cytoplasm. Then, these complexes translocate to the nucleus, and mediate the transcription of downstream target genes. The BMP/Smad signaling pathway is intricately regulated by extracellular or intracellular factors. Extracellular factors are BMP antagonists such as Noggin and sclerostin, and intracellular factors are Smads and their related molecules such as Smad6, Smad7, Tob, Ski, Smurf1, and Smurf2. Moreover, BMPs mediate the activation and crosstalk with other signaling pathways such as transforming growth factor-β and mitogen-activated protein kinase.22-24 Recently, Bieniasz et al demonstrated that there was a positive correlation between gene expression of vascular endothelial growth factor and BMP-2 in patients with lung cancer.25 In this study, we did not investigate how BMP-7 affects NSCLC progression at a molecular biological level. Therefore, in NSCLC progression, we still need to clarify the role of BMP-7 and factors related to the BMP signaling pathway.
In conclusion, the expression of BMP-7 in NSCLC was significantly associated with tumor progression and poorer prognosis. BMP-7 expression may be used as a predictor of postoperative outcome in NSCLC. Because BMP-7 activates many signaling molecules intricately involved in intracellular and extracellular factors and crosstalk with other signaling pathways, further analysis is needed to determine the exact mechanisms by which BMP-7 affects NSCLC progression.
Funding:
The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This study was supported by the Japan Society for the Promotion of Science KAKENHI Grant Number 24791466.
The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This study was supported by the Japan Society for the Promotion of Science KAKENHI Grant Number 24791466.
Declaration of Conflicting Interests:
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Author Contributions
MA, KK, MY and MS contributed to the design of the study. MA, GK, NI, SM, YN, TT, AHT and KM contributed to data collection and data analysis. MA, TU, YW, TN, TO and NY contributed to statistical analysis. MA and TU contributed to writing of the study. All authors gave final approval for the publication of the study.
MA, KK, MY and MS contributed to the design of the study. MA, GK, NI, SM, YN, TT, AHT and KM contributed to data collection and data analysis. MA, TU, YW, TN, TO and NY contributed to statistical analysis. MA and TU contributed to writing of the study. All authors gave final approval for the publication of the study.
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