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A combination of p300 and Braf expression in the diagnosis and prognosis of melanoma
BMC Cancer volume 14, Article number: 398 (2014)
To date only a handful of drugs are available for the treatment of melanoma. Among them vemurafenib, a BrafV600E specific inhibitor, showed promising results in terms of response rate and increase in median survival time. However, its effectiveness is limited by development of resistance and the search for additional drugs for melanoma treatment is ongoing. The present study was performed to analyze the correlation between Braf expression and the expression of p300, a known down stream target of the mitogen activated protein kinase (MAPK) pathway, which was recently shown by us to be a prognostic marker for melanoma progression and patient survival.
The expression of Braf and p300 expression were correlated and analyzed by Chi-square test. A total of 327 melanoma patient cases (193 primary melanoma and 134 metastatic melanoma) were used for the study. Classification & regression tree (CRT), Kaplan-Meier, and multivariate Cox regression analysis were used to elucidate the significance of the combination of Braf and p300 expression in the diagnosis and prognosis of melanoma.
Our results demonstrate that Braf expression is inversely correlated with nuclear p300 and positively correlated with cytoplasmic p300 expression. Braf and cytoplasmic p300 were found to be associated with melanoma progression, tumor size and ulceration status. CRT analysis revealed that a combination of Braf and p300 expression (nuclear and cytoplasmic), could be used to distinguish between nevi and melanoma, and primary from metastatic melanoma lesions. The combination of Braf and nuclear p300 was significantly associated with patient survival and nuclear p300 was found to be an independent predictor of patient survival.
Our results indicate a cross-talk between Braf and p300 in melanoma and demonstrate the importance Braf and p300 expression in the diagnosis and prognosis of melanoma.
Melanoma, a type of cancer caused due to uncontrolled proliferation of melanocytes in epidermis of skin, is one of the most frequent cancers in fair skinned populations [1, 2]. According to recently published statistics based on data from United States of America, it is the fifth most common cancer in men and seventh most common cancer in women . Melanoma is known for its rapid progression, metastasis, and poor prognosis, and is responsible for over 80% of deaths from skin cancer . Early diagnosis allows for surgical excision of the tumors and the patients can be managed with a relapse free interval of up to 10 years [4, 5]. But, approximately 1 in 35 patients develop metastatic tumors, and metastatic melanoma has a very poor prognosis with an overall survival between 8 to 18 months. Only 15% of patients with metastatic melanoma survive for 5 years [3, 6].
There has been limited progress in the treatment of melanoma; metastatic melanoma is notorious for its resistance to conventional radiotherapy and chemotherapy. Until recently, dacarbazine, a DNA alkylating agent, was the only FDA approved drug available for the treatment of melanoma . In 2011, vemurafenib, a specific inhibitor of BrafV600E (BRAF harbouring a point mutation resulting from a substitution of valine at amino-acid 600 with glutamine), and ipilimumab, a monoclonal antibody against cytotoxic T-lymphocyte associated antigen 4 (CTLA-4), have been approved for the treatment of melanoma . However, the success of their use is limited by effectiveness only in a restricted population, potential development of lethal resistance with vemurafenib treatment, and only a small increase in median survival time in the case of ipilimumab . Our lab previously reported a significant association between increased Braf expression and melanoma progression, and an inverse relationship between Braf expression and patient prognosis [7, 8]. Considering the significance of Braf inhibitors in melanoma treatment, several studies have attempted to decipher the mechanisms for resistance and suggested both mitogen activated protein kinase (MAP kinase) dependent and independent pathways as reasons for vemurafenib resistance . A number of strategies to overcome the resistance, including a combination therapy of Braf and MEK1/2 inhibitors, have been proposed and are in various stages of clinical studies . However, there are no results on the efficiency of the combination therapies in clinical settings and the search for alternative and additional drugs for the treatment of melanoma is ongoing.
We analyzed the expression of p300, a well studied histone acetyl transferase (HAT) , in melanoma patient samples and found that loss of p300 expression in the nucleus was correlated with disease progression and worse survival in melanoma patients . Furthermore, we also found that nuclear p300 expression was an independent prognostic factor, suggesting the importance of targeting the functions of histone acetyltransferases (HAT) in melanoma therapy . Stability and activity of p300 protein have been shown to be regulated by phosphorylation, and phosphorylation of p300 by mitogen activated protein kinase (MAPK) and extracellular signal-regulated kinase (ERK1/2) has been reported to promote the degradation of p300 protein [11, 12]. Since our previous studies in melanoma patients showed an increase in Braf expression, which is known to be upstream of MAPK in the signaling cascade, we hypothesized a potential for correlation between p300 and Braf . To test our hypothesis, and to explore the possible opportunity of targeting histone acetylation and Braf in melanoma treatment, we studied the association between p300 and Braf expression in patient samples.
Patient specimens and tissue microarray construction
The collection of patient specimens and the construction of the tissue microarray (TMA) have been previously described . Briefly, we used patient data collected from 1990 to 2009. Of 748 patients specimens collected, 369 biopsies including 327 melanoma cases (193 primary melanoma and 134 metastatic melanoma) and 42 cases of nevi (21 normal nevi and 21 dysplastic nevi) could be evaluated for comparing p300 and Braf staining in this study, due to loss of biopsy cores or insufficient tumor cells present in the cores. The demographic characteristics of melanoma patients are detailed in Table 1. All specimens were obtained from the archives of the Department of Pathology, Vancouver General Hospital. The use of human skin tissues and the waiver of patient consent in this study were approved by the Clinical Research Ethics Board of the University of British Columbia . The study was conducted according to the principles expressed in the Declaration of Helsinki.
From the original tissue biopsies, the most representative tumor area was carefully selected and marked on hematoxylin and eosin stained slides. Tissue cores of 0.6-mm thickness were taken in duplicate from each biopsy and the TMAs were assembled using a tissue-array instrument (Beecher Instruments, Silver Spring, MD). Using a Leica microtome, multiple 4 μM sections were cut and transferred to adhesive-coated slides using regular histological procedures. One section from each TMA was routinely stained with hematoxylin and eosin while the remaining sections were stored at room temperature for immunohistochemical staining.
Tissue microarray (TMA) slides were dewaxed at 55°C for 20 min followed by three 5 min washes with xylene. The tissues were then rehydrated by washing the slides for 5 min each with 100%, 95%, 80% ethanol and finally with distilled water. The slides were then heated to 95°C for 30 min in 10 mmol/L sodium citrate (pH 6.0) for antigen retrieval and then treated with 3% hydrogen peroxide for 1 hour to block the endogenous peroxidase activity. After blocking the slides with the universal blocking serum (Dako Diagnostics, Carpinteria, CA, USA), the sections were incubated overnight with monoclonal mouse anti-p300 antibody (1:50 dilution; Millipore, USA) or with mouse polyclonal anti-Braf antibody (1:100 dilution; Sigma, USA) at 4°C. The sections were then incubated for 30 min with a biotin-labeled secondary antibody and then with streptavidin-peroxidase (Dako Diagnostics). The samples were developed by treatment with 3,3′-diamino-benzidine substrate (Vector Laboratories, Burlington, Ontario, Canada) and with hematoxylin to counter-stain the nuclei. Negative controls were done by omitting the p300/Braf antibody during the primary antibody incubation.
Evaluation of immunostaining
The evaluation of p300 and Braf staining was done blindly by microscopic examination of the tissue sections by one dermatopathologist and two other observers simultaneously, using a multiple viewing microscope and a consensus was reached for the score of each core. p300/Braf staining intensity was scored as 0+, 1+, 2+, 3+ whereas the percentage of p300/Braf positive cells was scored as 1 (1-25%), 2 (26-50%), 3 (51-75%) and 4 (76-100%). In cases of discrepancy between duplicated cores, the higher score from the two tissue cores was taken as the final score. The product of intensity and percentage was taken as the immunoreactive score (IRS) . Based on IRS, p300 & Braf staining in the tissue sections was categorized as negative (IRS 0), weak (IRS 1–4), moderate (IRS 6–8), or strong (IRS 9–12). Since p300 was found to be expressed in both nucleus and cytoplasm , the nuclear and cytoplasmic staining was evaluated in parallel at the same time. The choice of the optimum cut-off values for the IRS were derived based on the IRS pattern in nevi and melanoma cases and are described previously [7, 10].
Correlation between p300 and Braf, and clinicopathologic parameters was evaluated by Chi-square test among the patient subgroups. Survival time was calculated from the date of melanoma diagnosis to the date of death or last follow-up. The effect of p300 and Braf on the overall and disease-specific survival was evaluated by Kaplan-Meier analysis and log-rank test. Additionally, multivariate Cox proportional hazards regression models were preformed to estimate the hazard ratios (HRs) and their 95% confidential intervals (CIs). Classification tree was constructed by the classification and regression tree (CRT) model as described previously to examine possibility of using a Braf and p300 combination to identify different stages of melanoma . The decision trees depicting the classification rules were generated through recursive partitioning. When growing each tree, equal prior probabilities to the normal and cancer cohorts, and equal misclassification costs were assigned. To assess the amount of over-fitting, 10-fold cross-validation experiments was performed using the SE rule as described previously . P-value <0.05 was considered as statistically significant. All the statistical analyses were performed using SPSS version 16.0 (SPSS Inc, Chicago, IL) software.
Braf expression correlates inversely with nuclear p300 and directly with cytoplasmic p300 expression
Previous studies showed that phosphorylation by MAP kinase resulted in accelerated degradation of p300 in cardiac cells . Since Braf is known to be an up stream kinase in the MAP kinase pathway, we asked if its expression could be inversely associated with p300 expression in the tumor samples from melanoma patients. Based on the previously reported cut-off values for immunoreactive scores (IRS), we divided the staining into low (IRS 0 to 4) and high (IRS 6 to 12), and matched the expression of Braf and p300 in the melanoma patients [7, 10]. Chi-square analysis of the matched data revealed that Braf expression inversely correlated with nuclear p300 and directly correlated with cytoplasmic p300 expression suggesting Braf negatively regulates the nuclear accumulation of p300 (Figure 1A & B).
Braf and cytoplasmic p300 expression are associated with disease progression
We next asked if the association between Braf and p300 expression was particularly correlated with disease progression or tumor size or ulceration status. We first divided the data based on American Joint Committee for Cancer (AJCC) staging and performed Chi-square test analysis. As shown in Table 2, the percentage of patients with high Braf expression or high cytoplasmic expression was significantly increased as melanoma progressed from AJCC stage I to stage III and then slightly decreased from stage III to stage IV. Accordingly, the percentage of patients with high Braf and high cytoplasmic p300 expression was significantly increased from AJCC stage I through stage III and slightly decreased from stage III to stage IV (Figure 1C). Interestingly, the difference in percentage of patients with high Braf and high cytoplasmic p300 expression was highest between stage I and II, which differ mainly based on the tumor size (Figure 1C) . On the other hand, increase in the percentage of cases with high Braf and low nuclear p300 expression was more apparent between stages II and III, which differ based on the presence of tumor cells in the lymph nodes, an indicator of migration and metastasis (Table 2) .
Next we separated the cases based on tumor size (≤2 mm versus >2 mm) and then based on ulceration status (no ulceration versus ulceration). Braf expression was found to be significantly associated with tumor size and ulceration status, whereas cytoplasmic p300 expression was associated with tumor size but not with ulceration status (Table 3). Nuclear p300 expression was not associated with tumor size or ulceration status (Table 3). As seen with melanoma progression, the incidence of larger tumors was significantly higher (Figure 1C), and presence of ulcerated tumors tended to be higher (Figure 1D), in patients with high Braf and high cytoplasmic p300 expression. Though patients with low nuclear p300 tended to be associated with advanced stages of melanoma, larger tumor size and presence of ulcerated tumors, the difference did not reach statistical significance (Table 3).
Combination of Braf and p300 in the diagnosis of melanoma
Since we found Braf and p300 to be significantly associated with markers of advanced melanoma stages, we asked if a combination of Braf and p300 expression could be used to separate nevi from melanoma in skin biopsies. Classification and regression tree (CRT) analysis of the patient expression data was previously shown to be useful in differentiating nevi and melanoma . We categorized the nevi and melanoma values as dependent variables and Braf, nuclear p300 and cytoplasmic p300 expression as independent variables, and performed CRT analysis on the data. As seen in Figure 2, Braf expression was the best marker to predict melanoma cases, followed by cytoplasmic p300 expression and nuclear p300 expression. We then used CRT analysis to test if the combination of Braf and p300 could be used to classify the primary melanoma cases and metastatic melanoma cases. As seen in Figure 3, cytoplasmic p300 expression was the best marker to separate the primary melanoma from metastatic melanoma cases, which could be further classified, using Braf and nuclear p300 expression.
Combination of Braf and p300 in patient prognosis
In order to test the significance of Braf and p300 in patient prognosis, we analyzed the correlation between Braf and p300 expression and patient survival using Kaplan-Meier analysis. We first confirmed the previously reported association between nuclear p300 and patient survival, and then tested a combination of Braf and nuclear p300 and studied the 5-year patient survival. As seen in Figure 4A & B, patients with low nuclear p300 expression had significantly worse 5-year survival. Intriguingly, patients with high Braf and low nuclear p300 had significantly worse 5-year survival, and patients with low Braf and high nuclear p300 had better 5-year survival, indicating the opposing effects of Braf and nuclear p300 on patient survival (Figure 5A & B). On the other hand, a combination of cytoplasmic p300 and Braf expression tended to be associated with worse prognosis and the patients with high Braf and high cytoplasmic p300 had the worst 5-year overall and disease-specific survival compared to the other categories (Figure 5C & D). However, the differences were not strong enough and failed to reach statistical significance.
Nuclear p300 expression independently regulates patient survival
We then performed multivariate Cox regression analysis to test if Braf and/or p300 expression could independently regulate the patient survival. We used AJCC staging, nuclear p300, cytoplasmic p300, and Braf expression as variables in the model. As shown in Table 4, multivariate Cox regression analysis revealed that AJCC staging and nuclear p300 were significantly associated with patient survival, whereas the association between Braf and cytoplasmic p300, and patient survival did not reach statistical significance. Our results are in line with the previously published data showing that Braf expression was not an independent prognostic factor. It was suggested that due to the close association with the AJCC stages, tumor size and ulceration status, Braf expression could not independently predict patient survival .
The key to successful management of melanoma includes both early and accurate diagnosis, followed by medical intervention in the form of surgery and chemotherapy. Accuracy of the diagnosis is particularly important as misdiagnosis of the melanoma patients might lead to inadequate treatment and allow spread of the disease. Melanoma is distinguished from dysplastic nevi with a fair degree of success using routine pathological examination, but ambiguous lesions could still pose problems due to the wide variation in morphologic features and because of the overlap in the clinical and histologic features between dysplastic nevi and melanoma [16, 18–21]. Our results suggest that a combination of Braf and p300 expression can be used for differentiating melanoma from nevi. The protocol for immunohistochemical staining of the tissue samples is a simple technique to perform and can give results relatively fast . Since the expression of only two markers is needed to completely separate nevi from melanoma, the experimental costs are also relatively small. Our study could thus be used to develop a practical protocol, which would complement routine pathological examination and provide a clarification when tissue sections show overlapping morphologic and histologic features.
Despite significant progress in the identification of molecular pathways that drive tumorigenesis, melanoma still poses a challenge to the scientific community. Owing to its notorious resistance to chemotherapy, patients with malignant melanoma have limited treatment options and have a poor prognosis. Although, vemurafenib, a BrafV600E specific inhibitor, showed impressive results in terms of response rate and progression free survival, the responses are mostly short-lived as seen by development of resistance in nearly every case [23–25]. Several strategies to increase the effectiveness, like combining Braf inhibitors with MEK1/2 inhibitors or small molecule inhibitors of the PI-3 kinase pathway, are in various stages of clinical studies, but it is too early to predict their clinical efficacy [6, 25].
Our results from patient survival show that patients with low Braf and high nuclear p300 expression have better survival, hinting at the benefits of simultaneously targeting Braf and nuclear p300 in treatment of melanoma. Data from our previous study showed that though cytoplasmic p300 expression was significantly associated with clinico-pathologic characteristics of melanoma, only nuclear p300 had prognostic significance . Even in the present study, cytoplasmic p300 expression was only informative during the diagnosis part of the analysis but was not a significant prognostic factor (Table 4). Besides, the major site of activity of p300 is in the nucleus where it regulates critically important processes like transcription and DNA repair [26–28]. Interestingly, loss of another well known histone acetyltransferase, TIP60, was reported to be associated with worse prognosis in melanoma patients . We therefore think that combining Braf inhibitors with HDAC inhibitors might be beneficial in the chemotherapy of melanoma. Strikingly, two HDAC inhibitors, vorinostat (Merck) and romidepsin (Gloucester Pharmaceuticals), which reportedly showed inhibitory effects on melanoma growth, were approved by the US FDA for the treatment of cutaneous T-cell lymphoma [30–34]. A combination of tyrosine kinase & C-Raf inhibitor, Sorafenib and vorinostat is currently being studied in the treatment of advanced cancers , but we could not find any studies performed using a combination of B-raf inhibitors and vorinostat or romidepsin. Our findings encourage further research on the potential improved efficacy of coadministration of Braf and HDAC inhibitors.
Another finding of our study is the inverse correlation between Braf and nuclear p300 and direct correlation between Braf and cytoplasmic p300 expression which suggests possible cross-talk between Braf and p300. Previous studies showed that phosphorylation of p300 could differentially regulate its activity and protein stability [36, 37]. For example, while protein kinase C (PKC) and salt inducible kinase 2 mediated phosphorylation at serine-89 was reported to inhibit the HAT activity [38, 39], Akt mediated phosphorylation at serine-1834, serine-2279, serine-2315, and serine-2366 was shown to enhance the HAT activity of p300 [40–42]. Along those lines, Akt and ERK2 mediated phosphorylation was shown to stabilize p300 protein levels, but phosphorylation by mitogen activated protein kinase (MAPK) resulted in degradation of the p300 protein [11, 12, 36, 40, 43]. However, none of the studies have so far focused on the effect of phosphorylation on intracellular distribution of p300. Our findings point to the possible phosphorylation and altered localization of p300 by Braf/MAPK signaling, which needs further investigation.
While our database was relatively large with details of several clinical characteristics, further studies are warranted before drawing firm conclusions on the benefits of combined Braf and HDAC inhibitors. Though the significance of finding a correlation in patient biopsies cannot be underestimated, evidence from studies at the cellular level is needed to convincingly establish the relationship between Braf and p300. Furthermore, we did not have enough cases with information on the status of Braf mutations, so we were unable to analyze the potential correlation between BrafV600E and p300.
Our study elucidates the cross talk between Braf and p300 in melanoma and suggests that Braf might negatively regulate the accumulation of p300 in the nucleus and promote the cytoplasmic localization of p300. We also show that using a combination of Braf and p300 expression, it is possible to separate nevi and melanoma samples, and primary and metastatic melanoma samples. We show that patients with low Braf and high p300 expression have better prognosis, suggesting the possibility of combining Braf and HDAC inhibitors in melanoma treatment.
Miller AJ, Mihm MC: Melanoma. N Engl J Med. 2006, 355 (1): 51-65. 10.1056/NEJMra052166.
Rastrelli M, Alaibac M, Stramare R, Chiarion Sileni V, Montesco MC, Vecchiato A, Campana LG, Rossi CR: Melanoma m (zero): diagnosis and therapy. ISRN Dermatol. 2013, 2013: 616170-
Siegel R, Naishadham D, Jemal A: Cancer statistics, 2013. CA Cancer J Clin. 2013, 63 (1): 11-30. 10.3322/caac.21166.
Turner RM, Bell KJ, Morton RL, Hayen A, Francken AB, Howard K, Armstrong B, Thompson JF, Irwig L: Optimizing the frequency of follow-up visits for patients treated for localized primary cutaneous melanoma. J Clin Oncol. 2011, 29 (35): 4641-4646. 10.1200/JCO.2010.34.2956.
Bilimoria KY, Raval MV, Bentrem DJ, Wayne JD, Balch CM, Ko CY: National assessment of melanoma care using formally developed quality indicators. J Clin Oncol. 2009, 27 (32): 5445-5451. 10.1200/JCO.2008.20.9965.
Finn L, Markovic SN, Joseph RW: Therapy for metastatic melanoma: the past, present, and future. BMC Med. 2012, 10: 23-10.1186/1741-7015-10-23.
Safaee Ardekani G, Jafarnejad SM, Khosravi S, Martinka M, Ho V, Li G: Disease progression and patient survival are significantly influenced by BRAF protein expression in primary melanoma. Br J Dermatol. 2013, 169 (2): 320-328. 10.1111/bjd.12351.
Safaee Ardekani G, Jafarnejad SM, Tan L, Saeedi A, Li G: The prognostic value of BRAF mutation in colorectal cancer and melanoma: a systematic review and meta-analysis. PLoS One. 2012, 7 (10): e47054-10.1371/journal.pone.0047054.
Roth SY, Denu JM, Allis CD: Histone acetyltransferases. Annu Rev Biochem. 2001, 70: 81-120. 10.1146/annurev.biochem.70.1.81.
Rotte A, Bhandaru M, Cheng Y, Sjoestroem C, Martinka M, Li G: Decreased expression of nuclear p300 is associated with disease progression and worse prognosis of melanoma patients. PLoS One. 2013, 8 (9): e75405-10.1371/journal.pone.0075405.
Poizat C, Puri PL, Bai Y, Kedes L: Phosphorylation-dependent degradation of p300 by doxorubicin-activated p38 mitogen-activated protein kinase in cardiac cells. Mol Cell Biol. 2005, 25 (7): 2673-2687. 10.1128/MCB.25.7.2673-2687.2005.
Wang SA, Hung CY, Chuang JY, Chang WC, Hsu TI, Hung JJ: Phosphorylation of p300 increases its protein degradation to enhance the lung cancer progression. Biochim Biophys Acta. 2014, 1843 (6): 1135-1149. 10.1016/j.bbamcr.2014.02.001.
Zhang Z, Chen G, Cheng Y, Martinka M, Li G: Prognostic significance of RUNX3 expression in human melanoma. Cancer. 2011, 117 (12): 2719-2727. 10.1002/cncr.25838.
Chen G, Cheng Y, Zhang Z, Martinka M, Li G: Cytoplasmic Skp2 expression is increased in human melanoma and correlated with patient survival. PLoS One. 2011, 6 (2): e17578-10.1371/journal.pone.0017578.
Remmele W, Stegner HE: [Recommendation for uniform definition of an immunoreactive score (IRS) for immunohistochemical estrogen receptor detection (ER-ICA) in breast cancer tissue]. Pathologe. 1987, 8 (3): 138-140.
Zhang G, Li G: Novel multiple markers to distinguish melanoma from dysplastic nevi. PLoS One. 2012, 7 (9): e45037-10.1371/journal.pone.0045037.
Balch CM, Gershenwald JE, Soong SJ, Thompson JF, Atkins MB, Byrd DR, Buzaid AC, Cochran AJ, Coit DG, Eggermont AM DS, Flaherty KT, Gimotty PA, Kirkwood JM, McMasters KM, Mihm MC, Morton DL, Ross MI, Sober AJ, Sondak VK: Final version of 2009 AJCC melanoma staging and classification. J Clin Oncol. 2009, 27 (36): 6199-6206. 10.1200/JCO.2009.23.4799.
Pellacani G, Longo C, Ferrara G, Cesinaro AM, Bassoli S, Guitera P, Menzies SW, Seidenari S: Spitz nevi: In vivo confocal microscopic features, dermatoscopic aspects, histopathologic correlates, and diagnostic significance. J Am Acad Dermatol. 2009, 60 (2): 236-247. 10.1016/j.jaad.2008.07.061.
Duffy K, Grossman D: The dysplastic nevus: from historical perspective to management in the modern era: part II. Molecular aspects and clinical management. J Am Acad Dermatol. 2012, 67 (1): 19 e11-12. quiz 31–12
Duffy K, Grossman D: The dysplastic nevus: from historical perspective to management in the modern era: part I. Historical, histologic, and clinical aspects. J Am Acad Dermatol. 2012, 67 (1): 1 e1-16. 10.1016/j.jaad.2011.02.032. quiz 17–18
Rabkin MS: The limited specificity of histological examination in the diagnosis of dysplastic nevi. J Cutan Pathol. 2008, 35 (Suppl 2): 20-23.
Camp RL, Neumeister V, Rimm DL: A decade of tissue microarrays: progress in the discovery and validation of cancer biomarkers. J Clin Oncol. 2008, 26 (34): 5630-5637. 10.1200/JCO.2008.17.3567.
Chapman PB, Hauschild A, Robert C, Haanen JB, Ascierto P, Larkin J, Dummer R, Garbe C, Testori A, Maio M, Hogg D, Lorigan P, Lebbe C, Jouary T, Schadendorf D, Ribas A, O'Day SJ, Sosman JA, Kirkwood JM, Eggermont AMM, Dreno B, Nolop K, Li J, Nelson B, Hou J, Lee RJ, Flaherty KT, McArthur GA, for the BRIM-3 Study Group: Improved survival with vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med. 2011, 364 (26): 2507-2516. 10.1056/NEJMoa1103782.
Flaherty KT, Puzanov I, Kim KB, Ribas A, McArthur GA, Sosman JA, O’Dwyer PJ, Lee RJ, Grippo JF, Nolop K, Chapman PB: Inhibition of mutated, activated BRAF in metastatic melanoma. N Engl J Med. 2010, 363 (9): 809-819. 10.1056/NEJMoa1002011.
Kudchadkar R, Paraiso KH, Smalley KS: Targeting mutant BRAF in melanoma: current status and future development of combination therapy strategies. Cancer J. 2012, 18 (2): 124-131. 10.1097/PPO.0b013e31824b436e.
Iyer NG, Ozdag H, Caldas C: p300/CBP and cancer. Oncogene. 2004, 23 (24): 4225-4231. 10.1038/sj.onc.1207118.
Reed SH: Nucleotide excision repair in chromatin: damage removal at the drop of a HAT. DNA Repair (Amst). 2011, 10 (7): 734-742. 10.1016/j.dnarep.2011.04.029.
Tillhon M, Cazzalini O, Nardo T, Necchi D, Sommatis S, Stivala LA, Scovassi AI, Prosperi E: p300/CBP acetyl transferases interact with and acetylate the nucleotide excision repair factor XPG. DNA Repair (Amst). 2012, 11 (10): 844-852. 10.1016/j.dnarep.2012.08.001.
Chen G, Cheng Y, Tang Y, Martinka M, Li G: Role of Tip60 in human melanoma cell migration, metastasis, and patient survival. J Invest Dermatol. 2012, 132 (11): 2632-2641. 10.1038/jid.2012.193.
Giannini G, Cabri W, Fattorusso C, Rodriquez M: Histone deacetylase inhibitors in the treatment of cancer: overview and perspectives. Future Med Chem. 2012, 4 (11): 1439-1460. 10.4155/fmc.12.80.
Haigentz M, Kim M, Sarta C, Lin J, Keresztes RS, Culliney B, Gaba AG, Smith RV, Shapiro GI, Chirieac LR Mariadason JM, Belbin TJ, Greally JM, Wright JJ, Haddadf RI: Phase II trial of the histone deacetylase inhibitor romidepsin in patients with recurrent/metastatic head and neck cancer. Oral Oncol. 2012, 48 (12): 1281-1288. 10.1016/j.oraloncology.2012.05.024.
Murakami T, Sato A, Chun NA, Hara M, Naito Y, Kobayashi Y, Kano Y, Ohtsuki M, Furukawa Y, Kobayashi E: Transcriptional modulation using HDACi depsipeptide promotes immune cell-mediated tumor destruction of murine B16 melanoma. J Invest Dermatol. 2008, 128 (6): 1506-1516. 10.1038/sj.jid.5701216.
Landreville S, Agapova OA, Matatall KA, Kneass ZT, Onken MD, Lee RS, Bowcock AM, Harbour JW: Histone deacetylase inhibitors induce growth arrest and differentiation in uveal melanoma. Clin Cancer Res. 2012, 18 (2): 408-416. 10.1158/1078-0432.CCR-11-0946.
Dekker FJ, Haisma HJ: Histone acetyl transferases as emerging drug targets. Drug Discov Today. 2009, 14 (19–20): 942-948.
Dasari A, Gore L, Messersmith WA, Diab S, Jimeno A, Weekes CD, Lewis KD, Drabkin HA, Flaig TW, Camidge DR: A phase I study of sorafenib and vorinostat in patients with advanced solid tumors with expanded cohorts in renal cell carcinoma and non-small cell lung cancer. Invest New Drugs. 2013, 31 (1): 115-125. 10.1007/s10637-012-9812-z.
Wang QE, Han C, Zhao R, Wani G, Zhu Q, Gong L, Battu A, Racoma I, Sharma N, Wani AA: p38 MAPK- and Akt-mediated p300 phosphorylation regulates its degradation to facilitate nucleotide excision repair. Nucleic Acids Res. 2013, 41 (3): 1722-1733. 10.1093/nar/gks1312.
Chen J, Li Q: Life and death of transcriptional co-activator p300. Epigenetics. 2011, 6 (8): 957-961. 10.4161/epi.6.8.16065.
Bricambert J, Miranda J, Benhamed F, Girard J, Postic C, Dentin R: Salt-inducible kinase 2 links transcriptional coactivator p300 phosphorylation to the prevention of ChREBP-dependent hepatic steatosis in mice. J Clin Invest. 2010, 120 (12): 4316-4331. 10.1172/JCI41624.
Yuan LW, Gambee JE: Phosphorylation of p300 at serine 89 by protein kinase C. J Biol Chem. 2000, 275 (52): 40946-40951. 10.1074/jbc.M007832200.
Chen J, Halappanavar SS, St-Germain JR, Tsang BK, Li Q: Role of Akt/protein kinase B in the activity of transcriptional coactivator p300. Cell Mol Life Sci. 2004, 61 (13): 1675-1683.
Huang WC, Chen CC: Akt phosphorylation of p300 at Ser-1834 is essential for its histone acetyltransferase and transcriptional activity. Mol Cell Biol. 2005, 25 (15): 6592-6602. 10.1128/MCB.25.15.6592-6602.2005.
Liu Y, Denlinger CE, Rundall BK, Smith PW, Jones DR: Suberoylanilide hydroxamic acid induces Akt-mediated phosphorylation of p300, which promotes acetylation and transcriptional activation of RelA/p65. J Biol Chem. 2006, 281 (42): 31359-31368. 10.1074/jbc.M604478200.
Chen YJ, Wang YN, Chang WC: ERK2-mediated C-terminal serine phosphorylation of p300 is vital to the regulation of epidermal growth factor-induced keratin 16 gene expression. J Biol Chem. 2007, 282 (37): 27215-27228. 10.1074/jbc.M700264200.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/14/398/prepub
MB, GA, GZ, GL were supported by funds from Canadian Institute of Health Research (CCI-117958, MOP-110974, MOP-93810), KM was supported by funds from Canadian Dermatology Foundation. The funding organizations had no role in study design; in the collection, analysis, and interpretation of data; in the writing of the manuscript; and in the decision to submit the manuscript for publication.
The authors declare that they have no competing interests.
Conceived and designed the project: AR, analyzed the data: MB, MM, GA, GL, GZ, AR, and KM, wrote the manuscript: AR, KM and MB. All authors read and approved the final manuscript.
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Bhandaru, M., Ardekani, G.S., Zhang, G. et al. A combination of p300 and Braf expression in the diagnosis and prognosis of melanoma. BMC Cancer 14, 398 (2014) doi:10.1186/1471-2407-14-398
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