- Research article
- Open Access
BAP31, a promising target for the immunotherapy of malignant melanomas
- Shaojuan Yu†1, 2,
- Fuli Wang†3,
- Li Fan1, 4,
- Yuying Wei1,
- Haitao Li1,
- Yuanjie Sun1,
- Angang Yang1,
- Boquan Jin1,
- Chaojun Song1Email author and
- Kun Yang1Email author
© Yu et al.; licensee BioMed Central. 2015
- Received: 29 December 2014
- Accepted: 1 April 2015
- Published: 18 April 2015
Malignant melanoma’s (MM) incidence is rising faster than that of any other cancer in the US and the overall survival at 5 years is less than 10%. B cell associated protein 31 (BAP31) is overexpressed in most MMs and might be a promising target for immunotherapy of this disease.
Firstly, we investigated the expression profiles of human BAP31 (hBAP31) and mouse BAP31 (mBAP31) in human and mouse normal tissues, respectively. The expression level of hBAP31 in human MMs and mBAP31 in B16 melanoma cells was also analyzed. Then we constructed novel mBAP31 DNA vaccines and tested there ability to stimulate mBAP31-specific immune responses and antitumor immunity in B16 melanoma-bearing mice.
For the first time, we found that protein expression of hBAP31 were dramatically upregulated in human MMs when compared with human normal tissues. Predominant protein expression of mBAP31 was found in mouse B16 melanoma cells but not in mouse important organs. When mice were immunized with mBAP31 DNA vaccines, strong cellular response to mBAP31 was observed in the vaccinated mice. CTLs isolated from immunized mice could effectively kill mBAP31-positive target mouse B16 melanoma tumor cells in vitro and vaccination with mBAP31 DNA vaccines had potent anti-tumor activity in therapeutic model using B16 melanoma cells.
These are the first data supporting a vaccine targeting BAP31 that is capable of inducing effective immunity against BAP31-expressing MMs and will be applicable to human MMs and hBAP31 DNA vaccine warrants investigation in human clinical trials.
- Malignant melanomas
- Cancer immunotherapy
- DNA vaccine
Cancer malignancies are among the most life-threatening diseases worldwide . MM consists approximately 3% of all cancers and its incidence continues to rise. Although treated by adequate surgery, the overall survival of MM at 5 years is less than 10%. For disseminated MM, the appropriate systemic medical treatment is still controversial [2,3]. Identification of new tumor antigens expressed in melanoma and progresses in the molecular biology and immunotherapy should in the near future translate into molecular-based therapeutic strategies . Followed the discovery of a lot of tumor antigens and development of novel strategies, cancer immunotherapy has significantly developed during the last decades and completes the therapeutic arsenal [5,6]. Human preclinical trials of immunotherapy based on the newly defined tumor antigens highly expressed by MMs have now been reported and cast new light on the therapeutic strategies of the disease [7,8].
BAP31 is an ER chaperon that associates with newly synthesized integral membrane proteins and controls their fate. BAP31 is an integral ER-resident membrane protein and a component of several large protein complexes . In addition to its role as ER chaperon, BAP31 plays an important role in apoptosis. BAP31 could act as a regulator of procaspase-8 L processing  and could be cleaved by caspase-8 [11,12]. The cleaved BAP31 fragment, p20, is a potent inducer of apoptosis when expressed ectopically. Prominent BAP31 protein expression is restricted to a minority of cells in normal human tissues although its RNA transcripts are ubiquitously expressed [13,14].
For the first time, we found that protein expression of hBAP31 were dramatically upregulated in human MM tissues when compared with human normal tissues, with a total positive rate of 86.5% (122 of 141 cases). And predominant protein expression of mBAP31 was found in mouse B16 melanoma cells but not in mouse important organs. So we hypothesized that BAP31 might be used as a promising immunotherapy target for MMs. In this study we constructed mBAP31 DNA vaccines and lysosome-associated membrane protein (LAMP) was used to enhance the immune response against mBAP31. LAMP can target and bind the endosome/lysosome through the LAMP transmembrane/cytoplasmic domain. The luminal domain of LAMP is then integrated into the lysosome. Consequently, one strategy commonly is to insert the target DNA into LAMP as a LAMP/antigen chimera and could greatly enhance the immune response against a number of antigens [15,16]. When C57BL/6 mice were immunized with LAMP-mBAP31 chimera DNA vaccine or mBAP31 DNA vaccine, strong cellular response to mBAP31 was observed and no autoimmune disorders were observed in the vaccinated mice. Moreover, CTLs isolated from mBAP31 DNA vaccine immunized C57BL/6 mice could effectively kill mBAP31-positive target mouse B16 melanoma tumor cells in vitro. Furthermore, in a therapeutic model, vaccination with mBAP31 DNA vaccine had potent anti-tumor activity even in the established B16 melanoma. These are the first data supporting a vaccine targeting BAP31 that will be applicable to human MMs.
Mice and cell lines
All animal studies were conducted under a protocol approved by Animal Care Research Advisory Committee of Fourth Military Medical University and all experiments involving mice were according to the Guidelines of the Animal Research Ethics Board of Fourth Military Medical University. All experiments involving mice were performed under fully anesthetized by inhalation of a mixture of oxygen with 5% isoflurane, and all efforts were made to minimize suffering.
Female C57BL/6 (H-2b) mice (8 weeks old) were maintained and treated in accordance with recommendations for the proper use and care of laboratory animals. 293 T, mouse colon carcinoma cell line CT26 (H-2d) and mouse melanoma cell line B16 (H-2b) were purchased from American Type Culture Collection (ATCC) and cultured according to standard guidelines.
Sections were firstly dewaxed and hydrated. Endogenous peroxidase activity was blocked with methanol containing 3% H2O2 for 10 min, and nonspecific binding was blocked by normal goat serum (10%) for 10 min. The sections were then dipped into mAbs specific for human or mouse BAP31 developed in our lab. Normal mouse IgG was applied as negative control. After three washes in PBS, the slices were dipped into biotin-conjugated goat anti-mouse IgG (promega) for 1 h at room temperature followed by streptavidin-HRP complex incubation for another 1 h. Then antibody complexes were visualized by incubation with DAB chromogen. Sections were counterstained with Mayer’s hematoxylin for 30 s, dehydrated through gradient ethanol, cleared in dimethyl benzene, mounted, and examined using light microscopy.
Small interference RNA
The mammalian expression vector, pSUPER.retro.circular.stuffer (OligoEngine), was used for expression of siRNA in B16 cells. The gene-specific insert specifies a 19-nucleotide sequence (ggtgaacctccagaacaat) corresponding to nucleotides 339–357 downstream of the transcription start site of mBAP31, which is separated by a 9-nucleotide non-complementary spacer (tctcttgaa) from the reverse complement of the same 19-nucleotide sequence. This vector was referred to as pSUPER-mBAP31. A control vector (pSUPER-Control) was constructed using a 19-nucleotide sequence (gcgcgctttgtaggattcg) with no significant homology to any mammalian gene sequence and therefore serves as a non-silencing control (OligoEngine). These sequences were inserted into the pSUPER.retro.circular.stuffer backbone.
B16 cells, maintained in RPMI 1640 containing 10% FCS, were plated onto 6-well plates at 2 × 105 cells per well. After cultured in 37°C, 5%CO2 for 24 h, cells were transfected with 4 μg of RNAi plasmid hybrids using Lipofectamine 2000 reagent (Invitrogen) according to the manufacturer’s instructions. Stable transfected cell lines were screened and selected with 0.5 μg/ml puromycin (Sigma). Clonal cell lines were selected by Western blotting to confirm lack or low expression of mBAP31.
Western blotting analysis
Cell lysates (20 μg) were separated by SDS-PAGE and transferred onto Immobilon-P membrane (Millipore, Billerica, MA). The membrane was then blocked with 5% skim milk in PBST (0.29% Na2HPO4, 0.8% NaCl, 0.02% KCl, and 0.05% Tween-20, pH7.4) for 1 h at room temperature (RT) and then incubated with anti-mBAP31 mAb (diluted to 5 μg/mL) or control mAb for 1 h at RT. After washing three times with PBST, the membrane was incubated with HRP-conjugated goat anti-mouse IgG (1:1500 v/v, Promega) for 1 h at RT. Finally, the membrane was developed using an ECL kit (GE Healthcare) and exposed to Agfa x-ray film. Anti-β-actin mAb was used as internal standard for all samples.
Construction of DNA vaccine encoding mBAP31
The p43 and p43-LAMP vectors were kind gifts of Dr. August. Full length of mBAP31 was cloned, inserted into the vectors and termed p-mBAP31 and p-LAMP/mBAP31 respectively. The vaccination plasmids were produced by transforming Escherichia coli DH5a, and were then purified to remove endotoxin (Qiagen, Valencia, CA, USA). These plasmids were also constructed to carry enhanced green fluorescent protein (EGFP), p-mBAP31/EGFP and p-LAMP/mBAP31/EGFP, for expedient analysis of protein expression. EGFP-tagged protein expressions were studied by transfecting them into 293 T cell lines. EGFP expression was observed 24–48 h after transfection by fluorescence microscopy.
Immunization and evaluation of DNA vaccine immune response
Three groups female C57BL/6 mice were immunized subcutaneously at the base of the tail with 50 μg of the specified endotoxin-free DNA plasmid (p-mBAP31, p-LAMP/mBAP31) diluted in phosphate-buffered saline (PBS) or PBS as negative control. The mice were boosted twice every 3 weeks with the same plasmid. Immunized mice were observed of clinical manifestation of autoimmune diseases such as weight loss, hair/skin disorders, diarrhea or neurological disorders. 2 weeks after the third DNA injection, the frequency of cells producing IFN-γ in splenocytes was measured by ELISPOT. In briefly, Single cell suspensions depleted of red blood cells were prepared from freshly isolated immunized mouse splenocytes and washed 2 times with RPMI 1640 and then resuspended in RPMI 1640 contained 10% FBS. BAP31 specific IFN-γ production was determined by a standard ELISPOT assay following a 24 h incubation of splenocytes (106 per well) with synthetic overlapping mBAP31 peptides (1 μg/mL, 15-mer peptides spanning the mBAP31 protein, each overlapping the next by 9 amino acids). As a negative control, splenocytes cells were pulsed with the irrelevant 15-mer peptide of Hantaan virus (QTADWLSIIVYLTSF). ConA and recombinant mBAP31 (1 μg/mL) were used as positive controls.
Cytoxicity of CTLs of immunized mice was determined by quantitative measurements of the release of lactic dehydrogenase (LDH). The mouse melanoma B16 cells (H-2b), colon carcinoma CT26 cells (H-2d) or 2E8 cells (mBAP31-depleted B16 cells) were pulsed with or without corresponding peptides (2 μg/mL) and used as target cells. CD8+ cells, isolated from splenocytes of immunized C57BL/6 mice by magnetic beads conjugated with anti-CD8 mAbs (BD pharmingen), served as effector cells. CTL assays were performed with effector cells (E) and target cells (T) (1 × 104 cells/well) mixed together at ratios of 50:1, 25:1 or 12.5:1 in a final volume of 100 μl. After 4 h incubation at 37°C, 50 μl of the cultured supernatants was collected to assess the amount of LDH release using Non-Radioactive Cytotoxicity Assay kits (Promega). The percentage of target cell lysis was calculated from the following equation: 100 × (A-B)/(C-D), where A is the reading value of experimental signal, B is spontaneous background signal value of the effector cells, C is maximum signal value from target cells, and D is spontaneous background signal value of the target cells.
Therapeutic anti-tumor model of mBAP31 DNA vaccine in C57BL/6 mouse
C57BL/6 mice were transplanted subcutaneously with 5 × 104 B16 cells per mouse at day 0. On day 3, mice were randomized and divided into three groups (n = 8), immunized subcutaneously at the base of the tail with 50 μg of the DNA plasmid (p-mBAP31, p-LAMP/mBAP31) and PBS as negative control. Vaccination was repeated on days 10, 17, and 24 with the same plasmid. Tumor dimensions were measured serially, and tumor volumes were calculated using the following formula: long axis × (short axis)2 × 0.52 . On day 42, B16 melanoma tumor bearing mice from each group were sacrificed and the tumors were removed from the mice.
Differences of IFN-γ production in ELISPOT assays and tumor volumes in tumor therapeutic model in C57BL/6 mice were assessed using student t test. All P values are two tailed and all statistical analyses used SPSS 17.0 software. Differences at P < 0.05 were considered statistically significant.
Protein expression profiles of hBAP31 in human MMs
Protein expression profiles of hBAP31 in human normal tissues
Protein expression profiles of mBAP31 in mouse normal tissues
Expression of mBAP31 protein in B16 cells, CT26 cells and siRNA B16 cells
Western blot analysis was performed to determine the expression profiles of mBAP31 protein in B16 cells, CT26 cells and siRNA B16 cells. As shown in Additional file 2: Figure S2, there is a special 28KD band in the film suggesting high protein expression of mBAP31 in B16 cells and CT26 cells. B16 cells were then transfected with the pSUPER-mBAP31 or pSUPER-Control, and selected with puromycin for 3 weeks. The pSUPER-BAP31 and pSUPER-Control cells were cloned and analyzed BAP31 expression by Western blot. One pSUPER-mBAP31-transfected clonal cell line named 2E8 with a remarkable reduction in mBAP31 protein expression was obtained after cultured for 2 months compared with the pSUPER-Control transfected clonal cell line 1H12 and non-transfected B16 cells. Anti-β-actin mAb was used as internal standard for all samples.
Expression of mBAP31 protein in mBAP31 DNA vaccine transfected cells
The mBAP31 DNA vaccine was constructed with mouse homologue. The DNA vaccine must be able to express in mammalian cells for subsequent processing and presentation to T cells. To evaluate the expression levels of DNA vaccine vectors in mammalian cells, plasmids of EGFP-tagged mBAP31 and LAMP/mBAP31 were transfected into 293 T cells. The expression levels were analyzed by fluorescence microscopy and no significant difference in the fluorescence intensity of the transfected cells was observed, suggesting similar synthesis and translation rates for the two EGFP-tagged molecules (Additional file 3: Figure S3).
Vaccination with mBAP31 DNA vaccine could elicit high level of cellular immune responses in C57BL/6 mice
Vaccination with mBAP31 DNA vaccine elicits mBAP31-specific cytotoxic T cells
Vaccination with mBAP31 DNA vaccine suppresses tumor growth in a therapeutic model
For the first time, we found that protein expression of hBAP31 were dramatically upregulated in human MM tissues when compared with human normal tissues (lung, colon, rectum, liver, ovary, breast, cervix and esophagus), with a total positive rate of 86.5% (122 of 141 cases). And predominant protein expression of mBAP31 was found in mouse B16 melanoma cells but not in mouse important organs including brain, heart, colon, lung, liver, pancreas and kidney. Northern blotting analyses have revealed that BAP31 RNA transcripts are ubiquitously expressed, but prominent BAP31 protein expression analyzed by immunohistochemistry in our study and previous reports is restricted to a minority of cells in normal human tissues although its RNA transcripts are ubiquitously expressed [13,14]. The mechanism of the discrepancy of the expression level between the mRNA and protein of BAP31 should be investigated more intensely.
For a tumor antigen to be a promising immunotherapeutic target, the following properties would be crucial: 1) the protein expression should be documented by IHC analysis, and 2) the gene should have a reasonable frequency of expression, ideally in at least 10-20% of at least one or two tumor types . Using these two criteria, we have evaluated the BAP31, a gene product encoded by a gene located on Xq26, was hypothesized in the present study as a promisingly attractive vaccine target for human MMs.
The past five decades have witnessed a steady increase in the incidence of MMs . While early detection, appropriate surgery and, in some cases, adjuvant therapy have improved outcomes, at least one third of patients with early-stage melanoma will develop metastases. The prognosis for patients with metastatic melanoma remains dismal. Studies have shown that biochemotherapy (chemotherapy combined with interleukin-2 and interferon) was not associated with a statistically significant survival benefit in any of the individual trials or in a pooled analysis [21-26]. The emerging field of cancer immunotherapy offers a number of exciting promising treatments and cast new light on the therapeutic strategies of the disease [5,27-32].
Currently, cancer vaccine therapy for MMs has a 2-fold focus. On the one hand, advances have been aimed at improving the effectiveness of MM vaccines based on the identification of various MM associated antigens (i.e., MAGE, GAGE, SPANXC, SSX, etc.) [33-40]. On the other hand, the immune system also inadvertently plays a supportive role in promoting the development and progression of tumors [21,41]. Because tumor cells have multiple mechanisms to escape the cytotoxicity of the immune system, polyvalent vaccines are desirable, prompting searches for novel MM associated antigens.
BAP31 is an endoplasmic reticulum protein-sorting factor that associates with newly synthesized integral membrane proteins and controls their fate (i.e., egress, retention, survival, or degradation). For the first time, we identified high protein expression level of hBAP31 in human MM tissues, with a total positive rate of 86.5%. These results suggested that hBAP31 might be a promisingly attractive vaccine target for human MMs.. Moreover, our preliminary work suggested that depletion of BAP31 has a negative impact on the proliferation of tumor cells, indicating that BAP31 may play an important role in tumorigenesis. Further experiments showed that BAP31 might facilitate the resistance to apoptosis triggered by multiple chemotherapeutic drugs including cisplatin, VP-16 and taxol in vitro, which was used for the adjuvant chemotherapy various cancers (unpublished data).
To enhance the immune response against mBAP31 DNA vaccines, we developed a LAMP-mBAP31 chimera DNA vaccine based on previous reports on its function of enhancing T cell responses against various virus and tumor antigens. When C57BL/6 mice were immunized with LAMP-mBAP31 chimera DNA vaccine, stronger cellular response to mBAP31, CTL cytotoxicity and anti-tumor effects in the therapeutic model were observed than mice vaccinated with p-mBAP31 DNA vaccine. Moreover, no autoimmune disorders were observed in the vaccinated mice, suggesting the safety of vaccination with mBAP31 DNA vaccine. These are the first data supporting a vaccine targeting BAP31 that will be applicable to human MMs.
In conclusion, we demonstrated that immunization with a novel LAMP-mBAP31 chimera DNA vaccine can successfully generate mBAP31-specific anti-tumor immunity in mice supports further evaluation regarding the promising clinical efficacy of this vaccine and the preclinical trials is ongoing in our lab.
We thank for Dr. J. Thomas August for his kind gifts of p43 and p43-LAMP vectors. This work was partially supported by the National Natural Science Foundation of China (No.30901358, 81072116).
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