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针对前列腺癌的特异性免疫疗法中的靶分子。

Target molecules in specific immunotherapy against prostate cancer.

作者信息

Harada Mamoru, Noguchi Masanori, Itoh Kyogo

机构信息

Department of Immunology, Kurume University School of Medicine, 67 Asahi-machi, Kurume, Fukuoka 830-0011, Japan.

出版信息

Int J Clin Oncol. 2003 Aug;8(4):193-9. doi: 10.1007/s10147-003-0332-x.

DOI:10.1007/s10147-003-0332-x
PMID:12955573
Abstract

Recent advances in molecular biology and tumor immunology have allowed us to identify genes encoding human cancer-related antigens and their peptides that are recognized by cytotoxic T lymphocytes (CTLs). Although these advances have been preceded by studies on melanoma antigens, prostate cancer is another target candidate for specific immunotherapy. Several prostate tissue-specific antigens can be target molecules in specific immunotherapy for prostate cancer. The distribution of prostate tissue-specific antigens is more localized than that of melanoma-related antigens. Prostate-specific antigen (PSA) is available as an evaluation indicator of clinical course. In addition, epithelial cancer-related antigens are also applicable for prostate cancer patients. These lines of evidence suggest that prostate cancer is the best candidate for specific immunotherapy among the various types of epithelial cancers. A number of epitope peptides which have the potential to generate prostate cancer-reactive CTLs have been identified to date, and clinical trials targeting these molecules have been conducted. In this article, we review prostate cancer-related antigens and their epitope peptides, which have potential for use in the immunotherapy of prostate cancer patients, and we introduce the current status of clinical trials of specific immunotherapy targeting these molecules.

摘要

分子生物学和肿瘤免疫学的最新进展使我们能够识别编码人类癌症相关抗原及其肽段的基因,这些抗原和肽段可被细胞毒性T淋巴细胞(CTL)识别。尽管在黑色素瘤抗原研究之前就已经有了这些进展,但前列腺癌是特异性免疫治疗的另一个潜在靶点。几种前列腺组织特异性抗原可成为前列腺癌特异性免疫治疗的靶分子。前列腺组织特异性抗原的分布比黑色素瘤相关抗原更局限。前列腺特异性抗原(PSA)可作为临床病程的评估指标。此外,上皮癌相关抗原也适用于前列腺癌患者。这些证据表明,在各种类型的上皮癌中,前列腺癌是特异性免疫治疗的最佳候选对象。迄今为止,已经鉴定出许多有可能产生前列腺癌反应性CTL的表位肽,并且针对这些分子的临床试验已经开展。在本文中,我们综述了与前列腺癌相关的抗原及其表位肽,这些抗原和肽段有可能用于前列腺癌患者的免疫治疗,并且我们介绍了针对这些分子的特异性免疫治疗的临床试验现状。

相似文献

1
Target molecules in specific immunotherapy against prostate cancer.针对前列腺癌的特异性免疫疗法中的靶分子。
Int J Clin Oncol. 2003 Aug;8(4):193-9. doi: 10.1007/s10147-003-0332-x.
2
Advances in specific immunotherapy for prostate cancer.前列腺癌特异性免疫疗法的进展。
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Prostate stem cell antigen is a promising candidate for immunotherapy of advanced prostate cancer.前列腺干细胞抗原是晚期前列腺癌免疫治疗的一个有前景的候选者。
Cancer Res. 2000 Oct 1;60(19):5522-8.
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Identification of an HLA-A*0201-restricted T-cell epitope derived from the prostate cancer-associated protein trp-p8.鉴定一种源自前列腺癌相关蛋白trp-p8的HLA-A*0201限制性T细胞表位。
Prostate. 2003 Sep 1;56(4):270-9. doi: 10.1002/pros.10265.
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[Adaptive immunotherapy of the advanced prostate cancer - cancer testis antigen (CTA) as possible target antigens].[晚期前列腺癌的适应性免疫疗法——癌睾丸抗原(CTA)作为可能的靶抗原]
Aktuelle Urol. 2004 Aug;35(4):326-30. doi: 10.1055/s-2004-818510.
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Immunotherapy of prostate cancer.前列腺癌的免疫疗法。
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Human CTL epitopes prostatic acid phosphatase-3 and six-transmembrane epithelial antigen of prostate-3 as candidates for prostate cancer immunotherapy.人细胞毒性T淋巴细胞表位前列腺酸性磷酸酶-3和前列腺六次跨膜上皮抗原作为前列腺癌免疫治疗的候选物。
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[Human tumor-rejection antigens and peptides from genes to clinical research].[人类肿瘤排斥抗原及基因来源的肽段:从基因到临床研究]
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Prospects and limitations of recombinant poxviruses for prostate cancer immunotherapy.重组痘病毒用于前列腺癌免疫治疗的前景与局限性
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New epitope peptides derived from parathyroid hormone-related protein which have the capacity to induce prostate cancer-reactive cytotoxic T lymphocytes in HLA-A2+ prostate cancer patients.源自甲状旁腺激素相关蛋白的新表位肽,其能够在HLA-A2+前列腺癌患者中诱导前列腺癌反应性细胞毒性T淋巴细胞。
Prostate. 2005 Feb 15;62(3):233-42. doi: 10.1002/pros.20133.

引用本文的文献

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J Immunol Methods. 2016 Mar;430:43-50. doi: 10.1016/j.jim.2016.01.014. Epub 2016 Jan 28.
2
GPCR48/LGR4 promotes tumorigenesis of prostate cancer via PI3K/Akt signaling pathway.GPCR48/LGR4通过PI3K/Akt信号通路促进前列腺癌的肿瘤发生。
Med Oncol. 2015 Mar;32(3):49. doi: 10.1007/s12032-015-0486-1. Epub 2015 Jan 31.
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Reduced expression of NGEP is associated with high-grade prostate cancers: a tissue microarray analysis.
NGEP 表达降低与高级别前列腺癌相关:组织微阵列分析。
Cancer Immunol Immunother. 2013 Oct;62(10):1609-18. doi: 10.1007/s00262-013-1463-1. Epub 2013 Aug 17.
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DNA vaccination for prostate cancer, from preclinical to clinical trials - where we stand?用于前列腺癌的DNA疫苗接种:从临床前研究到临床试验——我们目前的进展如何?
Genet Vaccines Ther. 2012 Oct 9;10(1):9. doi: 10.1186/1479-0556-10-9.
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Immunological evaluation of personalized peptide vaccination monotherapy in patients with castration-resistant prostate cancer.免疫评估个体化肽疫苗单药治疗去势抵抗性前列腺癌患者。
Cancer Sci. 2010 Mar;101(3):601-8. doi: 10.1111/j.1349-7006.2009.01459.x. Epub 2009 Dec 7.
6
New gene expressed in prostate: a potential target for T cell-mediated prostate cancer immunotherapy.在前列腺中表达的新基因:T细胞介导的前列腺癌免疫治疗的潜在靶点。
Cancer Immunol Immunother. 2010 Jan;59(1):63-71. doi: 10.1007/s00262-009-0723-6. Epub 2009 Jun 4.
7
Guided selection of an anti-gamma-seminoprotein human Fab for antibody directed enzyme prodrug therapy of prostate cancer.用于前列腺癌抗体导向酶前药疗法的抗γ-精蛋白人Fab片段的导向选择。
Cancer Immunol Immunother. 2007 Apr;56(4):477-89. doi: 10.1007/s00262-006-0202-2. Epub 2006 Jul 26.
8
Tumor escape mechanisms in prostate cancer.前列腺癌中的肿瘤逃逸机制
Cancer Immunol Immunother. 2007 Jan;56(1):81-7. doi: 10.1007/s00262-005-0110-x. Epub 2005 Dec 16.
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Identification of parathyroid hormone-related protein-derived peptides immunogenic in human histocompatibility leukocyte antigen-A24+ prostate cancer patients.在人类组织相容性白细胞抗原 - A24阳性前列腺癌患者中具有免疫原性的甲状旁腺激素相关蛋白衍生肽的鉴定。
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