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Published in: Journal of Inflammation 1/2020

Open Access 01-12-2020 | Research

Prediction and identification of novel HLA-A*0201-restricted cytotoxic T lymphocyte epitopes from endocan

Authors: Gaohai Shao, Qingjun Liu, Ling Yang, Guibo Feng, Wang Zhao, Zhongyan Huang, Zhao Yang

Published in: Journal of Inflammation | Issue 1/2020

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Abstract

Background

Prediction and identification of cytotoxic T lymphocyte (CTL) epitopes from tumor associated antigens is a crucial step for the development of tumor immunotherapy strategy. Endocan has been identified as antigen overexpressed in various tumors.

Methods

In this experiment, we predicted and identified HLA-A2-restricted CTL epitopes from endocan by using the following procedures. Firstly, we predicted the epitopes from the amino acid sequence of endocan by computer-based methods; Secondly, we determined the affinity of the predicted peptide with HLA-A2.1 molecule by peptide-binding assay; Thirdly, we elicited the primary T cell response against the predicted peptides in vitro; Lastly, we tested the specific CTLs toward endocan and HLA-A2.1 positive target cells.

Results

These data demonstrated that peptides of endocan containing residues 4–12 and 9–17 could elicit specific CTLs producing interferon-γ and cytotoxicity.

Conclusions

Therefore, our findings suggested that the predicted peptides were novel HLA-A2.1-restricted CTL epitopes, and might provide promising target for tumor immunotherapy.
Literature
1.
go back to reference Lam FC, Morton SW, Wyckoff J, Vu Han TL, Hwang MK, et al. Enhanced efficacy of combined temozolomide and bromodomain inhibitor therapy for gliomas using targeted nanoparticles. Nat Commun. 2018;9:1991.PubMedPubMedCentralCrossRef Lam FC, Morton SW, Wyckoff J, Vu Han TL, Hwang MK, et al. Enhanced efficacy of combined temozolomide and bromodomain inhibitor therapy for gliomas using targeted nanoparticles. Nat Commun. 2018;9:1991.PubMedPubMedCentralCrossRef
2.
go back to reference Filbin MG, Tirosh I, Hovestadt V, Shaw ML, Escalante LE, et al. Developmental and oncogenic programs in H3K27M gliomas dissected by single-cell RNA-seq. Science. 2018;360:331–5.PubMedPubMedCentralCrossRef Filbin MG, Tirosh I, Hovestadt V, Shaw ML, Escalante LE, et al. Developmental and oncogenic programs in H3K27M gliomas dissected by single-cell RNA-seq. Science. 2018;360:331–5.PubMedPubMedCentralCrossRef
3.
go back to reference Komori T, Muragaki Y, Chernov MF. Pathology and genetics of Gliomas. Prog Neurol Surg. 2018;31:1–37.PubMedCrossRef Komori T, Muragaki Y, Chernov MF. Pathology and genetics of Gliomas. Prog Neurol Surg. 2018;31:1–37.PubMedCrossRef
4.
go back to reference Wong ET, Lok E, Swanson KD. Alternating electric fields therapy for malignant Gliomas: from bench observation to clinical reality. Prog Neurol Surg. 2018;32:180–95.PubMedCrossRef Wong ET, Lok E, Swanson KD. Alternating electric fields therapy for malignant Gliomas: from bench observation to clinical reality. Prog Neurol Surg. 2018;32:180–95.PubMedCrossRef
5.
go back to reference Paldor I, Chaichana KL, Brem H, Tyler BM. Targeted local therapy for Management of Intracranial High-Grade Gliomas. Prog Neurol Surg. 2018;32:159–71.PubMedCrossRef Paldor I, Chaichana KL, Brem H, Tyler BM. Targeted local therapy for Management of Intracranial High-Grade Gliomas. Prog Neurol Surg. 2018;32:159–71.PubMedCrossRef
6.
go back to reference Parker Kerrigan BC, Hossain A, Yamashita S, Lang FF. Stem cell therapy of Gliomas. Prog Neurol Surg. 2018;32:124–51.PubMedCrossRef Parker Kerrigan BC, Hossain A, Yamashita S, Lang FF. Stem cell therapy of Gliomas. Prog Neurol Surg. 2018;32:124–51.PubMedCrossRef
7.
go back to reference Qiu CR, Fu Q, Sui J, Zhang Q, Wei P, et al. Endocan: endothelial dysfunction, inflammation, or both? Angiology. 2017;68:80.PubMedCrossRef Qiu CR, Fu Q, Sui J, Zhang Q, Wei P, et al. Endocan: endothelial dysfunction, inflammation, or both? Angiology. 2017;68:80.PubMedCrossRef
8.
go back to reference Emet S, Elitok A, Onur I, Kocaaga M, Bilge AK, et al. Endocan: a novel biomarker associated with well-developed coronary collateral circulation in patients with stable angina and chronic total occlusion. J Thromb Thrombolysis. 2017;43:60–7.PubMedCrossRef Emet S, Elitok A, Onur I, Kocaaga M, Bilge AK, et al. Endocan: a novel biomarker associated with well-developed coronary collateral circulation in patients with stable angina and chronic total occlusion. J Thromb Thrombolysis. 2017;43:60–7.PubMedCrossRef
9.
go back to reference Sumei Z, Shaolong C, Xiang W, Yinliang Q, Qing Z, et al. Endocan reduces the malign grade of gastric cancer cells by regulating associated protein expression. Tumour Biol. 2016;37:14915–21.PubMedCrossRef Sumei Z, Shaolong C, Xiang W, Yinliang Q, Qing Z, et al. Endocan reduces the malign grade of gastric cancer cells by regulating associated protein expression. Tumour Biol. 2016;37:14915–21.PubMedCrossRef
10.
go back to reference Cornelius A, Cortet-Rudelli C, Assaker R, Kerdraon O, Gevaert MH, et al. Endothelial expression of endocan is strongly associated with tumor progression in pituitary adenoma. Brain Pathol. 2012;22:757–64.PubMedPubMedCentralCrossRef Cornelius A, Cortet-Rudelli C, Assaker R, Kerdraon O, Gevaert MH, et al. Endothelial expression of endocan is strongly associated with tumor progression in pituitary adenoma. Brain Pathol. 2012;22:757–64.PubMedPubMedCentralCrossRef
11.
go back to reference Roudnicky F, Poyet C, Wild P, Krampitz S, Negrini F, et al. Endocan is upregulated on tumor vessels in invasive bladder cancer where it mediates VEGF-A-induced angiogenesis. Cancer Res. 2013;73:1097–106.PubMedCrossRef Roudnicky F, Poyet C, Wild P, Krampitz S, Negrini F, et al. Endocan is upregulated on tumor vessels in invasive bladder cancer where it mediates VEGF-A-induced angiogenesis. Cancer Res. 2013;73:1097–106.PubMedCrossRef
12.
go back to reference Sagara A, Igarashi K, Otsuka M, Kodama A, Yamashita M, et al. Endocan as a prognostic biomarker of triple-negative breast cancer. Breast Cancer Res Treat. 2017;161:269–78.PubMedCrossRef Sagara A, Igarashi K, Otsuka M, Kodama A, Yamashita M, et al. Endocan as a prognostic biomarker of triple-negative breast cancer. Breast Cancer Res Treat. 2017;161:269–78.PubMedCrossRef
13.
go back to reference Huang X, Chen C, Wang X, Zhang JY, Ren BH, et al. Prognostic value of endocan expression in cancers: evidence from meta-analysis. Onco Targets Ther. 2016;9:6297–304.PubMedPubMedCentralCrossRef Huang X, Chen C, Wang X, Zhang JY, Ren BH, et al. Prognostic value of endocan expression in cancers: evidence from meta-analysis. Onco Targets Ther. 2016;9:6297–304.PubMedPubMedCentralCrossRef
14.
go back to reference Yang J, Sheng S, Yang Q, Li L, Qin S, et al. Endocan silencing induces programmed cell death in hepatocarcinoma. Oncol Lett. 2017;14:5333–9.PubMedPubMedCentral Yang J, Sheng S, Yang Q, Li L, Qin S, et al. Endocan silencing induces programmed cell death in hepatocarcinoma. Oncol Lett. 2017;14:5333–9.PubMedPubMedCentral
15.
go back to reference Mertoglu C, Gunay M, Yerligok O. Could Endocan, a marker of inflammation and endothelial dysfunction, be a new diagnostic marker for fibromyalgia? Clin Lab. 2018;64:405–10.PubMedCrossRef Mertoglu C, Gunay M, Yerligok O. Could Endocan, a marker of inflammation and endothelial dysfunction, be a new diagnostic marker for fibromyalgia? Clin Lab. 2018;64:405–10.PubMedCrossRef
16.
go back to reference Gaudet A, Portier L, Prin M, Copin MC, Tsicopoulos A, et al. (2019) Endocan regulates acute lung inflammation through control of leukocyte diapedesis. J Appl Physiol. 1985;127:668–78.CrossRef Gaudet A, Portier L, Prin M, Copin MC, Tsicopoulos A, et al. (2019) Endocan regulates acute lung inflammation through control of leukocyte diapedesis. J Appl Physiol. 1985;127:668–78.CrossRef
17.
go back to reference Liu H, Chen L, Liu J, Meng H, Zhang R, et al. Co-delivery of tumor-derived exosomes with alpha-galactosylceramide on dendritic cell-based immunotherapy for glioblastoma. Cancer Lett. 2017;411:182–90.PubMedCrossRef Liu H, Chen L, Liu J, Meng H, Zhang R, et al. Co-delivery of tumor-derived exosomes with alpha-galactosylceramide on dendritic cell-based immunotherapy for glioblastoma. Cancer Lett. 2017;411:182–90.PubMedCrossRef
18.
go back to reference Saito H, Kitagawa K, Yoneda T, Fukui Y, Fujsawa M, et al. Combination of p53-DC vaccine and rAd-p53 gene therapy induced CTLs cytotoxic against p53-deleted human prostate cancer cells in vitro. Cancer Gene Ther. 2017;24:289–96.PubMedCrossRef Saito H, Kitagawa K, Yoneda T, Fukui Y, Fujsawa M, et al. Combination of p53-DC vaccine and rAd-p53 gene therapy induced CTLs cytotoxic against p53-deleted human prostate cancer cells in vitro. Cancer Gene Ther. 2017;24:289–96.PubMedCrossRef
19.
go back to reference Choi CW, Jeong MH, Park YS, Son CH, Lee HR, et al. Combination treatment of stereotactic body radiation therapy and immature dendritic cell vaccination for augmentation of local and systemic effects. Cancer Res Treat. 2018. Choi CW, Jeong MH, Park YS, Son CH, Lee HR, et al. Combination treatment of stereotactic body radiation therapy and immature dendritic cell vaccination for augmentation of local and systemic effects. Cancer Res Treat. 2018.
20.
go back to reference Lanterna C, Musumeci A, Raccosta L, Corna G, Moresco M, et al. The administration of drugs inhibiting cholesterol/oxysterol synthesis is safe and increases the efficacy of immunotherapeutic regimens in tumor-bearing mice. Cancer Immunol Immunother. 2016;65:1303–15.PubMedCrossRef Lanterna C, Musumeci A, Raccosta L, Corna G, Moresco M, et al. The administration of drugs inhibiting cholesterol/oxysterol synthesis is safe and increases the efficacy of immunotherapeutic regimens in tumor-bearing mice. Cancer Immunol Immunother. 2016;65:1303–15.PubMedCrossRef
21.
go back to reference Jo J, Wen PY. Antiangiogenic therapy of high-grade Gliomas. Prog Neurol Surg. 2018;31:180–99.PubMed Jo J, Wen PY. Antiangiogenic therapy of high-grade Gliomas. Prog Neurol Surg. 2018;31:180–99.PubMed
22.
go back to reference Wesseling P, Capper D. WHO 2016 classification of gliomas. Neuropathol Appl Neurobiol. 2018;44:139–50.PubMedCrossRef Wesseling P, Capper D. WHO 2016 classification of gliomas. Neuropathol Appl Neurobiol. 2018;44:139–50.PubMedCrossRef
23.
go back to reference Mount CW, Majzner RG, Sundaresh S, Arnold EP, Kadapakkam M, et al. Potent antitumor efficacy of anti-GD2 CAR T cells in H3-K27M(+) diffuse midline gliomas. Nat Med. 2018;24:572–9.PubMedPubMedCentralCrossRef Mount CW, Majzner RG, Sundaresh S, Arnold EP, Kadapakkam M, et al. Potent antitumor efficacy of anti-GD2 CAR T cells in H3-K27M(+) diffuse midline gliomas. Nat Med. 2018;24:572–9.PubMedPubMedCentralCrossRef
24.
go back to reference Zhou Y, Tan Z, Chen K, Wu W, Zhu J, et al. Overexpression of SHCBP1 promotes migration and invasion in gliomas by activating the NF-kappaB signaling pathway. Mol Carcinog. 2018;57:1181–90.PubMedCrossRef Zhou Y, Tan Z, Chen K, Wu W, Zhu J, et al. Overexpression of SHCBP1 promotes migration and invasion in gliomas by activating the NF-kappaB signaling pathway. Mol Carcinog. 2018;57:1181–90.PubMedCrossRef
25.
go back to reference Ishikawa E, Muragaki Y, Yamamoto T, Ohno T, Matsumura A. Vaccine therapy of high-grade Gliomas. Prog Neurol Surg. 2018;32:101–11.PubMedCrossRef Ishikawa E, Muragaki Y, Yamamoto T, Ohno T, Matsumura A. Vaccine therapy of high-grade Gliomas. Prog Neurol Surg. 2018;32:101–11.PubMedCrossRef
26.
27.
go back to reference Butowski N. Novel and prospective molecular targets for therapy of intracranial Gliomas. Prog Neurol Surg. 2018;32:66–78.PubMedCrossRef Butowski N. Novel and prospective molecular targets for therapy of intracranial Gliomas. Prog Neurol Surg. 2018;32:66–78.PubMedCrossRef
28.
go back to reference Ciaglia E, Laezza C, Abate M, Pisanti S, Ranieri R, et al. Recognition by natural killer cells of N6-isopentenyladenosine-treated human glioma cell lines. Int J Cancer. 2018;142:176–90.PubMedCrossRef Ciaglia E, Laezza C, Abate M, Pisanti S, Ranieri R, et al. Recognition by natural killer cells of N6-isopentenyladenosine-treated human glioma cell lines. Int J Cancer. 2018;142:176–90.PubMedCrossRef
29.
go back to reference Zhu C, Chrifi I, Mustafa D, van der Weiden M, Leenen PJM, et al. CECR1-mediated cross talk between macrophages and vascular mural cells promotes neovascularization in malignant glioma. Oncogene. 2017;36:5356–68.PubMedPubMedCentralCrossRef Zhu C, Chrifi I, Mustafa D, van der Weiden M, Leenen PJM, et al. CECR1-mediated cross talk between macrophages and vascular mural cells promotes neovascularization in malignant glioma. Oncogene. 2017;36:5356–68.PubMedPubMedCentralCrossRef
30.
go back to reference Wildes TJ, Grippin A, Dyson KA, Wummer BM, Damiani DJ, et al. Cross-talk between T cells and hematopoietic stem cells during adoptive cellular therapy for malignant Glioma. Clin Cancer Res. 2018;24:3955–66.PubMedPubMedCentralCrossRef Wildes TJ, Grippin A, Dyson KA, Wummer BM, Damiani DJ, et al. Cross-talk between T cells and hematopoietic stem cells during adoptive cellular therapy for malignant Glioma. Clin Cancer Res. 2018;24:3955–66.PubMedPubMedCentralCrossRef
31.
go back to reference Baker GJ, Chockley P, Zamler D, Castro MG, Lowenstein PR. Natural killer cells require monocytic gr-1(+)/CD11b(+) myeloid cells to eradicate orthotopically engrafted glioma cells. Oncoimmunology. 2016;5:e1163461.PubMedPubMedCentralCrossRef Baker GJ, Chockley P, Zamler D, Castro MG, Lowenstein PR. Natural killer cells require monocytic gr-1(+)/CD11b(+) myeloid cells to eradicate orthotopically engrafted glioma cells. Oncoimmunology. 2016;5:e1163461.PubMedPubMedCentralCrossRef
32.
go back to reference Chitadze G, Lettau M, Luecke S, Wang T, Janssen O, et al. NKG2D- and T-cell receptor-dependent lysis of malignant glioma cell lines by human gammadelta T cells: modulation by temozolomide and a disintegrin and metalloproteases 10 and 17 inhibitors. Oncoimmunology. 2016;5:e1093276.PubMedCrossRef Chitadze G, Lettau M, Luecke S, Wang T, Janssen O, et al. NKG2D- and T-cell receptor-dependent lysis of malignant glioma cell lines by human gammadelta T cells: modulation by temozolomide and a disintegrin and metalloproteases 10 and 17 inhibitors. Oncoimmunology. 2016;5:e1093276.PubMedCrossRef
33.
go back to reference Orozco-Morales M, Sanchez-Garcia FJ, Golan-Cancela I, Hernandez-Pedro N, Costoya JA, et al. RB mutation and RAS overexpression induce resistance to NK cell-mediated cytotoxicity in glioma cells. Cancer Cell Int. 2015;15:57.PubMedPubMedCentralCrossRef Orozco-Morales M, Sanchez-Garcia FJ, Golan-Cancela I, Hernandez-Pedro N, Costoya JA, et al. RB mutation and RAS overexpression induce resistance to NK cell-mediated cytotoxicity in glioma cells. Cancer Cell Int. 2015;15:57.PubMedPubMedCentralCrossRef
34.
go back to reference Qin K, Tian G, Li P, Chen Q, Zhang R, et al. Anti-glioma response of autologous T cells stimulated by autologous dendritic cells electrofused with CD133+ or CD133- glioma cells. J Neuroimmunol. 2012;242:9–15.PubMedCrossRef Qin K, Tian G, Li P, Chen Q, Zhang R, et al. Anti-glioma response of autologous T cells stimulated by autologous dendritic cells electrofused with CD133+ or CD133- glioma cells. J Neuroimmunol. 2012;242:9–15.PubMedCrossRef
35.
go back to reference Chen H, Yuan B, Zheng Z, Liu Z, Wang S, et al. A novel vaccine containing EphA2 epitope and LIGHT plasmid induces robust cellular immunity against glioma U251 cells. Cell Immunol. 2011;272:102–6.PubMedCrossRef Chen H, Yuan B, Zheng Z, Liu Z, Wang S, et al. A novel vaccine containing EphA2 epitope and LIGHT plasmid induces robust cellular immunity against glioma U251 cells. Cell Immunol. 2011;272:102–6.PubMedCrossRef
36.
go back to reference Adach-Kilon A, Swiatek-Machado K, Kaminska B, Dabrowski M. Signal transducer and activator of transcription 1 (Stat1) maintains basal mRNA expression of pro-survival stat3-target genes in glioma C6 cells. J Cell Biochem. 2011;112:3685–94.PubMedCrossRef Adach-Kilon A, Swiatek-Machado K, Kaminska B, Dabrowski M. Signal transducer and activator of transcription 1 (Stat1) maintains basal mRNA expression of pro-survival stat3-target genes in glioma C6 cells. J Cell Biochem. 2011;112:3685–94.PubMedCrossRef
37.
go back to reference Liu Z, Poiret T, Persson O, Meng Q, Rane L, et al. NY-ESO-1- and survivin-specific T-cell responses in the peripheral blood from patients with glioma. Cancer Immunol Immunother. 2018;67:237–46.PubMedCrossRef Liu Z, Poiret T, Persson O, Meng Q, Rane L, et al. NY-ESO-1- and survivin-specific T-cell responses in the peripheral blood from patients with glioma. Cancer Immunol Immunother. 2018;67:237–46.PubMedCrossRef
38.
go back to reference Liu Y, Yuelling LW, Wang Y, Du F, Gordon RE, et al. Astrocytes promote Medulloblastoma progression through hedgehog secretion. Cancer Res. 2017;77:6692–703.PubMedPubMedCentralCrossRef Liu Y, Yuelling LW, Wang Y, Du F, Gordon RE, et al. Astrocytes promote Medulloblastoma progression through hedgehog secretion. Cancer Res. 2017;77:6692–703.PubMedPubMedCentralCrossRef
39.
go back to reference Liu H, Smith AJ, Ball SS, Bao Y, Bowater RP, et al. Sulforaphane promotes ER stress, autophagy, and cell death: implications for cataract surgery. J Mol Med (Berl). 2017;95:553–64.CrossRef Liu H, Smith AJ, Ball SS, Bao Y, Bowater RP, et al. Sulforaphane promotes ER stress, autophagy, and cell death: implications for cataract surgery. J Mol Med (Berl). 2017;95:553–64.CrossRef
40.
go back to reference van Kooyk Y, Unger WW, Fehres CM, Kalay H, Garcia-Vallejo JJ. Glycan-based DC-SIGN targeting vaccines to enhance antigen cross-presentation. Mol Immunol. 2013;55:143–5.PubMedCrossRef van Kooyk Y, Unger WW, Fehres CM, Kalay H, Garcia-Vallejo JJ. Glycan-based DC-SIGN targeting vaccines to enhance antigen cross-presentation. Mol Immunol. 2013;55:143–5.PubMedCrossRef
41.
go back to reference Eleveld-Trancikova D, Sanecka A, van Hout-Kuijer MA, Looman MW, Hendriks IA, et al. DC-STAMP interacts with ER-resident transcription factor LUMAN which becomes activated during DC maturation. Mol Immunol. 2010;47:1963–73.PubMedCrossRef Eleveld-Trancikova D, Sanecka A, van Hout-Kuijer MA, Looman MW, Hendriks IA, et al. DC-STAMP interacts with ER-resident transcription factor LUMAN which becomes activated during DC maturation. Mol Immunol. 2010;47:1963–73.PubMedCrossRef
42.
go back to reference Weng D, Calderwood SK, Gong J. A novel heat shock protein 70-based vaccine prepared from DC-tumor fusion cells. Methods Mol Biol. 2018;1709:359–69.PubMedCrossRef Weng D, Calderwood SK, Gong J. A novel heat shock protein 70-based vaccine prepared from DC-tumor fusion cells. Methods Mol Biol. 2018;1709:359–69.PubMedCrossRef
43.
go back to reference Turer CC, Durmus D, Balli U, Guven B. Effect of non-surgical periodontal treatment on gingival Crevicular fluid and serum Endocan, vascular endothelial growth factor-a, and tumor necrosis factor-alpha levels. J Periodontol. 2017;88:493–501.PubMedCrossRef Turer CC, Durmus D, Balli U, Guven B. Effect of non-surgical periodontal treatment on gingival Crevicular fluid and serum Endocan, vascular endothelial growth factor-a, and tumor necrosis factor-alpha levels. J Periodontol. 2017;88:493–501.PubMedCrossRef
44.
go back to reference Yassine H, De Freitas CN, Depontieu F, Scherpereel A, Awad A, et al. The non glycanated endocan polypeptide slows tumor growth by inducing stromal inflammatory reaction. Oncotarget. 2015;6:2725–35.PubMedCrossRef Yassine H, De Freitas CN, Depontieu F, Scherpereel A, Awad A, et al. The non glycanated endocan polypeptide slows tumor growth by inducing stromal inflammatory reaction. Oncotarget. 2015;6:2725–35.PubMedCrossRef
45.
go back to reference Abid MR, Yi X, Yano K, Shih SC, Aird WC. Vascular endocan is preferentially expressed in tumor endothelium. Microvasc Res. 2006;72:136–45.PubMedCrossRef Abid MR, Yi X, Yano K, Shih SC, Aird WC. Vascular endocan is preferentially expressed in tumor endothelium. Microvasc Res. 2006;72:136–45.PubMedCrossRef
47.
go back to reference Yu PH, Chou SF, Chen CL, Hung H, Lai CY, et al. Upregulation of endocan by Epstein-Barr virus latent membrane protein 1 and its clinical significance in nasopharyngeal carcinoma. PLoS One. 2013;8:e82254.PubMedPubMedCentralCrossRef Yu PH, Chou SF, Chen CL, Hung H, Lai CY, et al. Upregulation of endocan by Epstein-Barr virus latent membrane protein 1 and its clinical significance in nasopharyngeal carcinoma. PLoS One. 2013;8:e82254.PubMedPubMedCentralCrossRef
48.
go back to reference Matano F, Yoshida D, Ishii Y, Tahara S, Teramoto A, et al. Endocan, a new invasion and angiogenesis marker of pituitary adenomas. J Neuro-Oncol. 2014;117:485–91.CrossRef Matano F, Yoshida D, Ishii Y, Tahara S, Teramoto A, et al. Endocan, a new invasion and angiogenesis marker of pituitary adenomas. J Neuro-Oncol. 2014;117:485–91.CrossRef
49.
go back to reference Grigoriu BD, Depontieu F, Scherpereel A, Gourcerol D, Devos P, et al. Endocan expression and relationship with survival in human non-small cell lung cancer. Clin Cancer Res. 2006;12:4575–82.PubMedCrossRef Grigoriu BD, Depontieu F, Scherpereel A, Gourcerol D, Devos P, et al. Endocan expression and relationship with survival in human non-small cell lung cancer. Clin Cancer Res. 2006;12:4575–82.PubMedCrossRef
50.
go back to reference Delehedde M, Devenyns L, Maurage CA, Vives RR. Endocan in cancers: a lesson from a circulating dermatan sulfate proteoglycan. Int J Cell Biol. 2013;2013:705027.PubMedPubMedCentralCrossRef Delehedde M, Devenyns L, Maurage CA, Vives RR. Endocan in cancers: a lesson from a circulating dermatan sulfate proteoglycan. Int J Cell Biol. 2013;2013:705027.PubMedPubMedCentralCrossRef
Metadata
Title
Prediction and identification of novel HLA-A*0201-restricted cytotoxic T lymphocyte epitopes from endocan
Authors
Gaohai Shao
Qingjun Liu
Ling Yang
Guibo Feng
Wang Zhao
Zhongyan Huang
Zhao Yang
Publication date
01-12-2020
Publisher
BioMed Central
Published in
Journal of Inflammation / Issue 1/2020
Electronic ISSN: 1476-9255
DOI
https://doi.org/10.1186/s12950-020-00240-w

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