- Open Access
DJ-1 is activated in medulloblastoma and is associated with cell proliferation and differentiation
© Lin et al.; licensee BioMed Central Ltd. 2014
- Received: 4 June 2014
- Accepted: 18 November 2014
- Published: 5 December 2014
DJ-1 is a key regulator in human tumorigenesis, including brain malignancies. The mechanisms by which DJ-1 contributes to the pathogenesis of medulloblastoma (MB) remain unclear, and its impact on the prognosis for patients with MB has not been identified. The aim of this study was to determine whether the DJ-1 protein is associated with tumorigenesis of MBs, and whether DJ-1 is a valuable factor for predicting the prognosis of patients with MB.
We collected 66 pairs of MB and adjacent normal cerebellum samples. Expression of DJ-1, Ser 473-phosphorylated-Akt (p-Akt), PTEN, and Ki-67 (MIB-1) was detected by immunohistochemical staining, and the correlation of these immunostaining results with the clinicopathological features of patients with MB was determined.
High DJ-1 expression (48.5%, 32/66) in tumor cells of MBs was significantly associated with the classic MB variant (P = 0.003), high proliferative activity (P = 0.002) and undifferentiated tumor (P = 0.001), whereas high p-Akt expression (56.1%, 37/66) was associated with tumor metastasis stage (P = 0.007), undifferentiated tumor (P = 0.007), and high-risk tumor (P = 0.002). High DJ-1 expression also correlated with high p-Akt expression and high MIB-1 index. However, only high levels of DJ-1(P = 0.009) and high MIB-1 index (P = 0.001) were strong independent prognostic factors associated with worse overall survival.
Although the validity of the preliminary data in this study needs to be confirmed by a larger number of cases, our study indicates that DJ-1, PTEN, and p-Akt might play important roles in cell proliferation and differentiation of MBs. The evaluation of expression of DJ-1 and related proteins might be useful for predicting the prognosis of patients with MB.
- PI3K/Akt pathway
Medulloblastoma (MB) is the most common malignant tumor of central nervous system in children , while it rarely occurs in adults . Although multimodality treatment regimens, including surgery, radiotherapy (RT), and chemotherapy, have greatly improved disease outcome, about one-third of patients with MB remain incurable. Moreover, the 5-year disease survival rate is only 36% for patients with MB with tumor dissemination and recurrence [3, 4]. The accumulated studies in MB have come to a consensus that MB can be classified into four core subgroups: WNT (Wingless), SHH (Sonic hedgehog), Group 3, and Group 4 . Each of these subtypes has a distinct molecular profile and genomic defects, which are associated with varied clinical parameters and patient outcomes. However, despite extensive investigation, the mechanism underlying MB progression has not been fully elucidated. More precise prognostic predictors and more effective therapies for MBs are therefore required.
Recently, research evidence has suggested that DJ-1 plays a role in human tumorigenesis. DJ-1 is a 189 amino acid protein, and was originally identified as an oncogene that, in combination with H-RAS, can transform mouse NIH3T3 cells . The DJ-1 protein has been found in various malignant tumor cells, including prostate cancer, non-small cell lung cancer, laryngeal cancer, ovarian carcinoma, and cervical cancer, where it plays a role in increasing cell proliferation and metastasis [7–10]. However, the effect of DJ-1 on the development and progression of MB has not yet been investigated.
DJ-1 is considered to contribute to oncogenesis by upregulating protein kinase B (PKB/Akt)-mediated cell survival [6, 11]. Akt is a 57-kDa serine/threonine kinase, and is a central mediator involved in the signal transduction of various growth-controlling pathways that involve phosphatidylinositol 3′-kinase (PI3K). PI3K, activated by growth factors, catalyzes the phosphorylation of phosphatidylinositol (4,5)-biphosphate (PIP2) to phosphatidylinositol (3,4,5)-triphosphate (PIP3). PIP3 in turn recruits 3-phosphoinositide-dependent kinase (PDK), which phosphorylates and activates Akt . Phosphorylated Akt (p-Akt) plays a key role in multiple signaling pathways, including cell proliferation, apoptosis, and transcription . Basic research has demonstrated that DJ-1 could antagonize the tumor suppressor PTEN to inhibit the activity of the PTEN gene and finally promote the proliferation of tumor cells . PTEN is a key negative regulator of the PI3K-protein kinase B signaling pathway. In MBs, loss of heterozygosity of chromosome 10q is frequent at the position where PTEN is located (10q23.31) [14, 15]. Dysregulation of PTEN was found to contribute to overactivation of the PI3K/Akt signaling pathway [16, 17]. Thus, we hypothesized that DJ-1 might contribute to the progression of MB by regulating the PTEN and Akt pathways. However, we could not find any report about the relationship between DJ-1 and tumorigenesis of MBs, or the mechanisms involved.
In this study, we first examined the DJ-1, PTEN, and p-Akt expression in surgical MB tissue specimens and paired tumor-adjacent tissue specimens. The aim of this study was to determine whether the DJ-1 protein is associated with tumorigenesis of MBs, and if it would be a valuable factor for predicting the prognosis of patients with MB.
Patients and clinical management
In retrospective study, we examined 66 pairs of paraffin wax-embedded MB and adjacent normal cerebellum samples collected from the Pathology Department of the First Affiliated Hospital of Sun Yat-sen University and Tongjiang Hospital of Guangdong during the period of 2003 to 2012. None of the patients had received chemotherapy or RT before surgical treatment. All experimental protocols were carried out with the approval of the Committee on Use of Human & Animal Subjects in Teaching and Research of Sun Yat-sen University, according to the Helsinki Declaration.
All patients had undergone midline suboccipital craniectomy to resect the tumor completely or partially. Extent of resection was defined on the basis of surgical reports and/or postoperative images. Patients received different treatment protocols after surgery, based on age stratification. All patients under 3 years of age received chemotherapy after surgery with standard regimens consisting of six course of temozolomide, vincristine, and cisplatin. Patients aged over 3 years initially received RT. Postoperative RT was conducted using craniospinal irradiation (CSI), with a subsequent boost to the posterior fossa. Patients received a total dose ranging from 40 to 54 Gy. After RT, six courses of standard chemotherapy with temozolomide, vincristine, and cisplatin were also used for these patients. Imaging inspection was repeated at intervals of 3 to 6 months to evaluate treatment response, metastasis, and tumor recurrence. All 66 patients were given a follow-up investigation, and follow-up was terminated in March 2013.
All the samples were re-evaluated according to the criteria of the WHO classification  by two experienced pathologists, with differences resolved by careful discussion. Of the 66 case of MB, 50 (75.7%) were classified as classic MB, 14 (21.2%) as the desmoplastic variant, 1 (1.5%) as the large cell/anaplastic variant, and 1 as MB with myogenic differentiation (previously termed medullomyoblastoma).
Immunohistochemical staining and scoring
Serial sections 4 μm thick were cut from eah tissue block and mounted on aminopropyltriethoxysilane (APES)-coated glass slides. After routine preparation of slides, the sections were incubated with one of the following antibodies: rabbit anti-human monoclonal PTEN antibody (1:100 dilution; D4.3), p-Akt (Ser 473) rabbit monoclonal antibody (1:25; D9E) (both Cell Signaling technology, MA, USA), rabbit anti-human polyclonal DJ-1 antibody (1:100; FL-189; Santa Cruz Biotechnology, SantaCruz, CA, USA), or Ki-67 (1:100 dilution; MIB-1; Dako Co., Glostrup, Denmark) for 60 min, respectively. Slides were processed using a ChemMate Envision/horseradish peroxidase kit (Dako) for 30 min at room temperature, followed by development with diaminobenzidine (DAB) for visualization. Positive controls consisted of biopsies of prostate tissue containing carcinoma and normal parenchyma (for DJ-1 and PTEN) and breast cancer (p-Akt). Negative controls were prepared by substituting non-immune serum for primary antibodies.
Immunohistochemical staining evaluation was conducted as described previously . Scoring of the percentage of immunoreactive tumor cells was as follows: 0 (0%), 1 (1 to 10%), 2 (11 to 50%), and 3 (>50%). The staining intensity was visually scored and stratified as 0 (negative), 1 (weak), 2 (moderate), and 3 (strong). A final immunoreactivity score was obtained for each case by multiplying the percentage and the intensity score. The median score was 4.5. Thus, DJ-1, PTEN, and p-Akt protein expression levels were further classified as lower (when the score was less than 4.5) and higher (when it was greater than 4.5). In order to reduce variation, all immunohistochemical staining was separately evaluated and scored semiquantitatively by two pathologists without knowledge of the clinical data of patients. The final score for protein expression in each case was the mean of the scores given by the two observers.
The proliferative activity of tumor cells was evaluated by counting the Ki-67 (MIB-1) labeling index with image analysis (Olympus Cell D1; Soft Imaging System GmbH, Munster, Germany) counting at least 1000 tumor cells at high magnification (×40 objective) in fields with the largest number of positive cells. Tissues were considered to have a high MIB-1 index (MI) when the Ki-67 labeling value was greater than the mean Ki-67 labeling value of all 66 MBs.
Statistical analysis was performed using SPSS software (version 14.0 for Windows; SPSS Inc., Chicago, IL, USA). Qualitative data are presented as number and percent. The χ2 was used for comparison between groups, and P < 0.05 was considered significant. Overall survival (OS) was counted (months) from the date of diagnosis to the date of death or last follow-up before study closure. Kaplan-Meier method and Cox regression were used for survival analysis.
Ethics committee approval and patient consent
This study was approved by Sun Yat-sen University review board or ethics committee.
DJ-1, p-Akt, and PTEN expression in MBs
Correlation of DJ-1, p-Akt, and PTEN expression with the clinicopathological characteristics of medulloblastoma
Correlation between proteins expression and clinicopathological characteristics of patients with MB
Proliferative activity (Ki-67 value)b
Low (n = 34)
High (n = 32)
Low (n = 29)
High (n = 37)
≤3 (n = 19)
25.28 ± 7.59
>3 (n = 47)
26.77 ± 8.74
Male (n = 43)
25.80 ± 7.31
Female (n = 23)
27.36 ± 10.23
WHO histological subtype c
Classic (n = 50)
25.17 ± 7.75
Desmoplastic (n = 14)
30.03 ± 9.89
Fourth ventricle (n = 29)
26.65 ± 8.51
Outside fourth ventricle (n = 37)
26.11 ± 8.42
Residual tumor size
≤1.5 cm2 (n = 54)
25.75 ± 8.14
>1.5 cm2 (n = 12)
29.04 ± 9.38
M0 (n = 12)
28.20 ± 7.39
M1 (n = 54)
25.93 ± 8.61
Standard (n = 6)
30.50 ± 9.58
High (n = 60)
25.93 ± 8.25
Undifferentiated (n = 39)
27.28 ± 8.82
Differentiated (n = 27)
25.00 ± 7.71
Low (n = 34)
23.33 ± 6.22
High (n = 32)
29.54 ± 9.28
Low (n = 29)
25.13 ± 6.92
High (n = 37)
27.29 ± 9.38
Prognostic relevance of DJ-1 and p-Akt expression in MBs
Kaplan-Meier analysis for OS rate of patients with MB
Mean survival time, months
95% CI, months
44.96 ± 5.18
34.81 to 55.12
47.72 ± 2.72
42.95 to 52.48
47.16 ± 2.70
41.86 to 52.46
46.60 ± 4.10
38.56 to 54.64
WHO histological subtypeb
48.39 ± 2.41
43.66 to 53.12
41.39 ± 5.93
29.76 to 53.02
46.35 ± 3.84
38.82 to 53.88
Outside fourth ventricle
47.66 ± 2.61
42.44 to 52.87
Residual tumor size
37.78 ± 6.14
25.73 to 45.83
49.68 ± 2.28
45.19 to 54.16
42.08 ± 7.92
26.54 to 57.62
47.45 ± 2.33
42.87 to 52.02
46.64 ± 2.34
23.75 ± 5.20
46.84 ± 3.03
40.89 to 52.79
46.87 ± 3.52
39.96 to 53.78
53.29 ± 1.79
49.77 to 56.81
40.28 ± 3.79
32.84 to 47.71
47.76 ± 3.19
41.50 to 54.03
46.30 ± 3.23
39.97 to 52.63
Cox regression model for multivariate analyses of prognostic factor in MBs
95% confidence interval
Age (≤3 years versus >3 years)
0.140 to 1.118
Gender (male versus female)
0.485 to 4.160
WHO histological subtype (classic versus desmoplastic)
0.308 to 2.808
Tumor location (fourth ventricle versus outside fourth ventricle)
0.404 to 3.573
Residual tumor size (≤1.5 cm2versus >1.5 cm2)
0.139 to 1.102
Metastatic status (M0versus M1)
0.310 to 9.546
Tumor risk (standard versus high)
0.041 to 11.92
Differentiation (differentiated versus undifferentiated)
0.121 to 0.998
MIB-1 index (low versus high)
DJ-1 expression (low versus high)
p-Akt expression (low versus high)
0.217 to 2.698
MBs are a heterogenous group of highly malignant embryonal brain tumors . For many years, MBs have been stratified into high-risk and standard-risk groups according to age, metastatic stage at diagnosis, and extent of surgical resection. Standard-risk patients are those diagnosed at ages over 3 years, have no metastases at presentation, and have manageable residual tumor (<1.5 cm2) after surgery. High-risk patients are those do not fulfill these criteria , and these patients should receive more intensive treatment. A recent study has shown that the combination of chemotherapy and RT has improved the 5-year survival rate, which is now 55% to 76% for high-risk patients and 70% to 80% for standard-risk patients . However, in the present study, we found that there was no significant difference in OS of patients with different tumor risk, and tumor risk stratification was not an independent factor for predicting the prognosis of patients with MB. The different treatment protocols based on age stratification did not show any marked benefit for prognosis. These results indicate that risk-adapted treatments are not entirely suitable for all patients with MB. Hence, it is important to identify novel clinical and biological factors that can be used to predict treatment response and accurately select patients who may benefit from a more or less aggressive treatment, and to improve risk stratification.
The importance of DJ-1 in the progression of MBs has not been identified, although recent studies have demonstrated that the DJ-1 molecule is relevant to the various human tumors [20, 23–25]. In the human brain, DJ-1 has been observed in neurons  and non-neural cells . DJ-1 has also been associated with autosomal recessive early-onset parkinsonism, with loss of function of DJ-1 leading to neurodegeneration . In gliomas, the relationship between high DJ-1 expression and high-grade glioma has indicated that DJ-1 might play a role in the acceleration of glioma progression . In the current study, we found the first evidence that high DJ-1 expression was closely correlated with undifferentiated tumor and active proliferation of tumors. Survival analysis revealed that high DJ-1 expression was significantly associated with low OS in patients with MB. Moreover, on multivariate analysis, high DJ-1 expression emerged as an independent factor influencing the prognosis of patients with MB. These results indicate that DJ-1 may promote tumor progression and could be an independent prognostic factor by influencing cell proliferation and differentiation. To date, there is still no conclusive evidence that measures of cell proliferation have clinical utility, and the relevant studies have provided conflicting data. Some studies have shown an association between a simple evaluation of mitotic count and survival for children with MB [29, 30]; however, survival analyses do not support the use of the Ki-67/MIB-1 index as prognostic indicator , although high bromodeoxyuridine (BrdU) index (>20%) appeared to indicated worse prognosis in one study . In the present study, high MIB-1 index had a strong correlation with poor prognosis of patients with MB and may be an independent indicator of tumor. More importantly, high proliferative activity of tumor cells was associated with high expression of DJ-1 protein. These data suggest that the cell proliferation influencing the prognosis of patients with MB might be modulated, at least partly, by the pathway involving the DJ-1 molecule.
DJ-1 is considered to contribute to oncogenesis by upregulating PKB/Akt-mediated cell survival [6, 11]. However, in this study, however, we did not find an association between high p-Akt expression by tumor and high MIB-1 index of tumor cells, although high p-Akt expression was observed to correlate closely with tumor differentiation and metastasis.
Consistent with this result, p-Akt expression was not a prognostic indicator for predicting the prognosis of patients with MB. On the one hand, activated Akt was expressed at much higher levels in MB tumors compared with normal human cerebellum, indicating that p-Akt may be up-regulated in tumourigenesis and tumor progression of MBs, such as modulating tumor differentiation and promoting metastasis. On the other hand, activated Akt is an essential, but not the only, pathway in promoting cell proliferation of MBs.
In addition, in the current study, we found that the areas having high DJ-1 expression always overlapped with those having p-Akt high expression.
These results suggest that DJ-1 does indeed have a role in modulating the Akt pathway in MBs, but it might not be the only factor to influence activated Akt in tumor progression. Recent studies have demonstrated that several growth factor receptors involving the PI3K/Akt cascade in their signal transduction are expressed in MB, such as the insulin-like growth factor-I receptor, Tropomyosin-related kinase B (TrkB), Platelet-derived growth factor receptor-beta (PDGFRB), and c-Kit [33–35]. PI3K/Akt signaling has also been found to enhance the effects of Hedgehog in MB tumor cells and their cerebellar precursors [36, 37]. However, in the present study we did not detect co-expression of DJ-1 and p-Akt in the same tumor cell, which would have provided more direct evidence to elucidate their relationship and cooperative effect on the modulation of tumor progression. The precise mechanism of DJ-1, p-Akt, and related growth factor receptors in the development and progression of MBs will be investigated in further studies.
PTEN is another key negative regulator of the PI3K signaling pathway . As MBs are known to display allelic losses of chromosomal region 10q, where the PTEN tumor suppressor gene is located, we hypothesize that inactivation of PTEN could constitute a possible mechanism that might be responsible for Akt activation. Recent data showed that losses of 10q are associated with metastatic disease at diagnosis , and the PTEN mutation detected in another study occurred only in a recurrent tumor that also carried a p53 mutation . It seems that the frequency of PTEN mutations is low in MBs, and that mutation may be associated with a more aggressive or relapsing phenotype of the tumor. In the present study, we did not examine mutations of the PTEN gene. However, we found that PTEN was inactivated at the protein expression level. PTEN was significantly decreased in MB tumor cells compared with normal human cerebellum, indicating that inactivation of PTEN at the transcriptional level may also be involved in the regulation of PTEN and thus may influence the activation of Akt. Epigenetic inactivation of PTEN has recently been reported in several human tumors, including central nervous system tumors , but the related mechanisms of PTEN inactivation at the mRNA transcription level need to be clarified in further investigations.
In the current study, we found that high DJ-1 expression was closely associated with classic MBs, and the areas with high expression of DJ-1or p-Akt always coincided with the regions that had loss of PTEN expression. These regions were usually undifferentiated areas of classic MBs or internodular areas of desmoplastic MBs. However, expression of DJ-1 and p-Akt was decreased in intranodular areas of desmoplastic MBs, in which the tumor cells appeared to have varying degrees of neuronal differentiation. PTEN expression was also detectable in regions with neuronal differentiation. Therefore, we hypothesize that DJ-1and PTEN could modulate tumor cell differentiation via Akt pathway. DJ-1 is due to its effects on the PI3K signaling pathway, and may modulate PTEN function to produce hyperphosphorylation of Akt [6, 11]. Recent data have shown that PI3K/Akt signaling enhances the effects of Hedgehog in MBs and their cerebellar precursors, and that it may represent an indispensable precondition for the molecular realization of the Hedgehog signal [36, 37]. Inhibiting Hedgehog-dependent gene expression in MB can cause cell cycle arrest, consistent with the initiation of neuronal differentiation and loss of neuronal stem cell-like characteristics . Molecular analysis has identified that the desmoplastic variant of MB is associated with activation of the Hedgehog-Patched signaling pathway . The desmoplastic variant has been associated with a better prognosis than classic MB in some studies, although there is no significant difference in outcome for these two variants in our study. Thus, the DJ-1/PTEN/p-Akt/Hedgehog signaling system might play important roles in modulating cell differentiation and further influence the outcome of MBs. Thus, blocking cell growth and inducing cell differentiation in MBs by interfering with the DJ-1 protein and Hedgehog pathway might represent a novel approach to treat this tumor. In fact, some inhibitors of the Hedgehog pathway, such as cyclopamine and HhAntag, have been proven to cause the regression of murine tumor allografts in vivo, and induce rapid death of cells from freshly resected human MBs [44, 45].
Although the precise roles of DJ-1, PTEN and p-Akt in MBs have not been identified, our study indicates links between these molecules in their protein expression level in MBs, and the validity of preliminary data in this study needs to be confirmed by a larger number of cases. We consider that DJ-1, PTEN, and p-Akt might play important roles in cell proliferation and differentiation of MBs, and their expression levels might be useful parameters for predicting the prognosis of patients with MB. Of course, more rigorous investigations are necessary to clarify their intrinsic links.
This study was supported by Scientific Research Project of Guangdong Provincial Science and Technology (grant numbers 2010B060900104 and 2012A030400008).
- Stevens MC, Cameron AH, Muir KR, Parkes SE, Reid H, Whitwell H: Descriptive epidemiology of primary central nervous system tumours in children: a population-based study. Clin Oncol (R Coll Radiol). 1991, 3: 323-329. 10.1016/S0936-6555(05)80587-4.View ArticleGoogle Scholar
- Louis DN, Ohgaki H, Wiestler OD, Cavenee WK, Burger PC, Jouvet A, Scheithauer BW, Kleihues P: The 2007 WHO classification of tumours of the central nervous system. Acta Neuropathol. 2007, 114: 97-109. 10.1007/s00401-007-0243-4.PubMed CentralView ArticlePubMedGoogle Scholar
- Gajjar A, Chintagumpala M, Ashley D, Kellie S, Kun LE, Merchant TE, Woo S, Wheeler G, Ahern V, Krasin MJ, Fouladi M, Broniscer A, Krance R, Hale GA, Stewart CF, Dauser R, Sanford RA, Fuller C, Lau C, Boyett JM, Wallace D, Gilbertson RJ: Risk-adapted craniospinal radiotherapy followed by high-dose chemotherapy and stem-cell rescue in children with newly diagnosed medulloblastoma (St Jude Medulloblastoma-96): long-term results from a prospective, multicentre trial. Lancet Oncol. 2006, 7: 813-820. 10.1016/S1470-2045(06)70867-1.View ArticlePubMedGoogle Scholar
- Packer RJ, Gajjar A, Vezina G, Rorke-Adams L, Burger PC, Robertson PL, Bayer L, LaFond D, Donahue BR, Marymont MH, Muraszko K, Langston J, Sposto R: Phase III study of craniospinal radiation therapy followed by adjuvant chemotherapy for newly diagnosed average-risk medulloblastoma. J Clin Oncol. 2006, 24: 4202-4208. 10.1200/JCO.2006.06.4980.View ArticlePubMedGoogle Scholar
- Kool M, Korshunov A, Remke M, Jones DT, Schlanstein M, Northcott PA, Cho YJ, Koster J, Schouten-van Meeteren A, van Vuurden D, Clifford SC, Pietsch T, von Bueren AO, Rutkowski S, McCabe M, Collins VP, Bäcklund ML, Haberler C, Bourdeaut F, Delattre O, Doz F, Ellison DW, Gilbertson RJ, Pomeroy SL, Taylor MD, Lichter P, Pfister SM: Molecular subgroups of medulloblastoma: an international meta-analysis of transcriptome, genetic aberrations, and clinical data of WNT, SHH, Group 3, and Group 4 medulloblastomas. Acta Neuropathol. 2012, 123: 473-484. 10.1007/s00401-012-0958-8.PubMed CentralView ArticlePubMedGoogle Scholar
- Nagakubo D, Taira T, Kitaura H, Ikeda M, Tamai K, Iguchi-Ariga SM, Ariga H: DJ-1, a novel oncogene which transforms mouse NIH3T3 cells in cooperation with ras. Biochem Biophys Res Commun. 1997, 231: 509-513. 10.1006/bbrc.1997.6132.View ArticlePubMedGoogle Scholar
- Hod Y: Differential control of apoptosis by DJ-1 in prostate benign and cancer cells. J Cell Biochem. 2004, 92: 1221-1233. 10.1002/jcb.20159.View ArticlePubMedGoogle Scholar
- Bai J, Guo C, Sun W, Li M, Meng X, Yu Y, Jin Y, Tong D, Geng J, Huang Q, Qi J, Fu S: DJ-1 may contribute to metastasis of non-small cell lung cancer. Mol Biol Rep. 2012, 39: 2697-2703. 10.1007/s11033-011-1024-7.View ArticlePubMedGoogle Scholar
- Zhu XL, Wang ZF, Lei WB, Zhuang HW, Jiang HY, Wen WP: DJ-1: a novel independent prognostic marker for survival in glottic squamous cell carcinoma. Cancer Sci. 2010, 101: 1320-1325. 10.1111/j.1349-7006.2010.01531.x.View ArticlePubMedGoogle Scholar
- Davidson B, Hadar R, Schlossberg A, Sternlicht T, Slipicevic A, Skrede M, Risberg B, Flørenes VA, Kopolovic J, Reich R: Expression and clinical role of DJ-1, a negative regulator of PTEN, in ovarian carcinoma. Hum Pathol. 2008, 39: 87-95. 10.1016/j.humpath.2007.05.014.View ArticlePubMedGoogle Scholar
- Kim RH, Peters M, Jang Y, Shi W, Pintilie M, Fletcher GC, DeLuca C, Liepa J, Zhou L, Snow B, Binari RC, Manoukian AS, Bray MR, Liu FF, Tsao MS, Mak TW: DJ-1, a novel regulator of the tumor suppressor PTEN. Cancer Cell. 2005, 7: 263-273. 10.1016/j.ccr.2005.02.010.View ArticlePubMedGoogle Scholar
- Alessi DR, James SR, Downes CP, Holmes AB, Gaffney PR, Reese CB, Cohen P: Characterization of a 3-phosphoinositide-dependent protein kinase which phosphorylates and activates protein kinase Balpha. Curr Biol. 1997, 7: 261-269. 10.1016/S0960-9822(06)00122-9.View ArticlePubMedGoogle Scholar
- Song G, Ouyang G, Bao S: The activation of Akt/PKB signaling pathway and cell survival. J Cell Mol Med. 2005, 9: 59-71. 10.1111/j.1582-4934.2005.tb00337.x.View ArticlePubMedGoogle Scholar
- Bigner SH, Mark J, Friedman HS, Biegel JA, Bigner DD: Structural chromosomal abnormalities in human medulloblastoma. Cancer Genet Cytogenet. 1988, 30: 91-101. 10.1016/0165-4608(88)90096-9.View ArticlePubMedGoogle Scholar
- Griffin CA, Hawkins AL, Packer RJ, Rorke LB, Emanuel BS: Chromosome abnormalities in pediatric brain tumors. Cancer Res. 1988, 48: 175-180.PubMedGoogle Scholar
- Chow LM, Baker SJ: PTEN function in normal and neoplastic growth. Cancer Lett. 2006, 241: 184-196. 10.1016/j.canlet.2005.11.042.View ArticlePubMedGoogle Scholar
- Hartmann W, Digon-Söntgerath B, Koch A, Waha A, Endl E, Dani I, Denkhaus D, Goodyer CG, Sörensen N, Wiestler OD, Pietsch T: Phosphatidylinositol 3′-kinase/AKT signaling is activated in medulloblastoma cell proliferation and is associated with reduced expression of PTEN. Clin Cancer Res. 2006, 12: 3019-3027. 10.1158/1078-0432.CCR-05-2187.View ArticlePubMedGoogle Scholar
- Louis DN, Ohgaki H, Wiestler OD: WHO Classification of Tumours of the Central Nervous System. 2007, Lyon: IARC pressGoogle Scholar
- Wang C, Fang M, Zhang M, Li W, Guan H, Sun Y, Xie S, Zhong X: The positive correlation between DJ-1 and β-catenin expression shows prognostic value for patients with glioma. Neuropathology. 2013, 33: 628-636. 10.1111/neup.12041.View ArticlePubMedGoogle Scholar
- Varan A: Risk-adapted chemotherapy in childhood medulloblastoma. Expert Rev Anticancer Ther. 2001, 11: 771-780.View ArticleGoogle Scholar
- Ellison DW, Clifford SC, Gajjar A, Gilbertson RJ: What’s new in neuro-oncology? Recent advances in medulloblastoma. Eur J Paediatr Neurol. 2003, 7: 53-66. 10.1016/S1090-3798(03)00014-X.View ArticlePubMedGoogle Scholar
- Gilbertson RJ: Medulloblastoma: signaling a change in treatment. Lancet Oncol. 2004, 5: 209-218. 10.1016/S1470-2045(04)01424-X.View ArticlePubMedGoogle Scholar
- Hinkle DA, Mullett SJ, Gabris BE, Hamilton RL: DJ-1 expression in glioblastomas shows positive correlation with p53 expression and negative correlation with epidermal growth factor receptor amplification. Neuropathology. 2011, 31: 29-37. 10.1111/j.1440-1789.2010.01124.x.View ArticlePubMedGoogle Scholar
- Pei XJ, Wu TT, Li B, Tian X, Li Z, Yang QX: Increased expression of macrophage migration inhibitory factor and DJ-1 contribute to cell invasion and metastasis of nasopharyngeal carcinoma. Int J Med Sci. 2013, 11: 106-115.View ArticlePubMedGoogle Scholar
- Li Y, Cui J, Zhang CH, Yang DJ, Chen JH, Zan WH, Li B, Li Z, He YL: High-expression of DJ-1 and loss of PTEN associated with tumor metastasis and correlated with poor prognosis of gastric carcinoma. Int J Med Sci. 2013, 10: 1689-1697. 10.7150/ijms.7292.PubMed CentralView ArticlePubMedGoogle Scholar
- Rizzu P, Hinkle DA, Zhukareva V, Bonifati V, Severijnen LA, Martinez D, Ravid R, Kamphorst W, Eberwine JH, Lee VM, Trojanowski JQ, Heutink P: DJ-1 colocalizes with tau inclusions: a link between parkinsonism and dementia. Ann Neurol. 2004, 55: 113-118. 10.1002/ana.10782.View ArticlePubMedGoogle Scholar
- Bandopadhyay R, Kingsbury AE, Cookson MR, Reid AR, Evans IM, Hope AD, Pittman AM, Lashley T, Canet-Aviles R, Miller DW, McLendon C, Strand C, Leonard AJ, Abou-Sleiman PM, Healy DG, Ariga H, Wood NW, de Silva R, Revesz T, Hardy JA, Lees AJ: The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson’s disease. Brain. 2004, 127: 420-430. 10.1093/brain/awh054.View ArticlePubMedGoogle Scholar
- Bonifati V, Rizzu P, van Baren MJ, Schaap O, Breedveld GJ, Krieger E, Dekker MC, Squitieri F, Ibanez P, Joosse M, van Dongen JW, Vanacore N, van Swieten JC, Brice A, Meco G, van Duijn CM, Oostra BA, Heutink P: Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science. 2003, 299: 256-259. 10.1126/science.1077209.View ArticlePubMedGoogle Scholar
- Gilbertson RJ, Jaros E, Perry RH, Kelly PJ, Lunec J, Pearson AD: Mitotic percentage index: a new prognostic factor for childhood medulloblastoma. Eur J Cancer. 1997, 33: 609-615. 10.1016/S0959-8049(96)00516-3.View ArticlePubMedGoogle Scholar
- McManamy CS, Lamont JM, Taylor RE, Cole M, Pearson AD, Clifford SC, Ellison DW: United Kingdom Children’s Cancer Study Group: Morphophenotypic variation predicts clinical behavior in childhood non-desmoplastic medulloblastomas. J Neuropathol Exp Neurol. 2003, 62: 627-632.PubMedGoogle Scholar
- Ohta T, Watanabe T, Katayama Y, Kurihara J, Yoshino A, Nishimoto H, Kishimoto H: TrkA expression is associated with an elevated level of apoptosis in classic medulloblastomas. Neuropathology. 2006, 26: 170-177. 10.1111/j.1440-1789.2006.00678.x.View ArticlePubMedGoogle Scholar
- Ito S, Hoshino T, Prados MD, Edwards MS: Cell kinetics of medulloblastomas. Cancer. 1992, 70: 671-678. 10.1002/1097-0142(19920801)70:3<671::AID-CNCR2820700322>3.0.CO;2-P.View ArticlePubMedGoogle Scholar
- Wang JY, Del Valle L, Gordon J, Rubini M, Romano G, Croul S, Peruzzi F, Khalili K, Reiss K: Activation of the IGF-IR system contributes to malignant growth of human and mouse medulloblastomas. Oncogene. 2001, 20: 3857-3868. 10.1038/sj.onc.1204532.View ArticlePubMedGoogle Scholar
- MacDonald TJ, Brown KM, LaFleur B, Peterson K, Lawlor C, Chen Y, Packer RJ, Cogen P, Stephan DA: Expression profiling of medulloblastoma: PDGFRA and the RAS/MAPK pathway as therapeutic targets for metastatic disease. Nat Genet. 2001, 29: 143-152. 10.1038/ng731.View ArticlePubMedGoogle Scholar
- Chilton-Macneill S, Ho M, Hawkins C, Gassas A, Zielenska M, Baruchel S: C-kit expression and mutational analysis in medulloblastoma. Pediatr Dev Pathol. 2004, 7: 493-498. 10.1007/s10024-004-1116-7.View ArticlePubMedGoogle Scholar
- Klein RS, Rubin JB, Gibson HD, DeHaan EN, Alvarez-Hernandez X, Segal RA, Luster AD: SDF-1 alpha induces chemotaxis and enhances Sonic hedgehog-induced proliferation of cerebellar granule cells. Development. 2001, 128: 1971-1981.PubMedGoogle Scholar
- Rubin JB, Kung AL, Klein RS, Chan JA, Sun Y, Schmidt K, Kieran MW, Luster AD, Segal RA: A small-molecule antagonist of CXCR4 inhibits intracranial growth of primary brain tumors. Proc Natl Acad Sci U S A. 2003, 100: 13513-13518. 10.1073/pnas.2235846100.PubMed CentralView ArticlePubMedGoogle Scholar
- Martelli AM, Cocco L, Capitani S, Miscia S, Papa S, Manzoli FA: Nuclear phosphatidylinositol 3, 4, 5-trisphosphate, phosphatidylinositol 3-kinase, Akt, and PTen: emerging key regulators of anti-apoptotic signaling and carcinogenesis. Eur J Histochem. 2007, 51: 125-131.PubMedGoogle Scholar
- Reardon DA, Michalkiewicz E, Boyett JM, Sublett JE, Entrekin RE, Ragsdale ST, Valentine MB, Behm FG, Li H, Heideman RL, Kun LE, Shapiro DN, Look AT: Extensive genomic abnormalities in childhood medulloblastoma by comparative genomic hybridization. Cancer Res. 1997, 57: 4042-4027.PubMedGoogle Scholar
- Rasheed BK, Stenzel TT, McLendon RE, Parsons R, Friedman AH, Friedman HS, Bigner DD, Bigner SH: PTEN gene mutations are seen in high-grade but not in low-grade gliomas. Cancer Res. 1997, 57: 4187-4190.PubMedGoogle Scholar
- Baeza N, Weller M, Yonekawa Y, Kleihues P, Ohgaki H: PTEN methylation and expression in glioblastomas. Acta Neuropathol. 2003, 106: 479-485. 10.1007/s00401-003-0748-4.View ArticlePubMedGoogle Scholar
- Berman DM, Karhadkar SS, Hallahan AR, Pritchard JI, Eberhart CG, Watkins DN, Chen JK, Cooper MK, Taipale J, Olson JM, Beachy PA: Medulloblastoma growth inhibition by hedgehog pathway blockade. Science. 2002, 297: 1559-1561. 10.1126/science.1073733.View ArticlePubMedGoogle Scholar
- Thompson MC, Fuller C, Hogg TL, Dalton J, Finkelstein D, Lau CC, Chintagumpala M, Adesina A, Ashley DM, Kellie SJ, Taylor MD, Curran T, Gajjar A, Gilbertson RJ: Genomics identifies medulloblastoma subgroups that are enriched for specific genetic alterations. J Clin Oncol. 2006, 24: 1924-1931. 10.1200/JCO.2005.04.4974.View ArticlePubMedGoogle Scholar
- Romer J, Curran T: Targeting medulloblastoma: small-molecule inhibitors of the Sonic Hedgehog pathway as potential cancer therapeutics. Cancer Res. 2005, 65: 4975-4878. 10.1158/0008-5472.CAN-05-0481.View ArticlePubMedGoogle Scholar
- Sasai K, Romer JT, Lee Y, Finkelstein D, Fuller C, McKinnon PJ, Curran T: Shh pathway activity is down-regulated in cultured medulloblastoma cells: implications for preclinical studies. Cancer Res. 2006, 66: 4215-4222. 10.1158/0008-5472.CAN-05-4505.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.