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Malignant features of minipig melanomas prior to spontaneous regression.小型猪黑色素瘤自发消退前的恶性特征。
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Deciphering the immune reaction leading to spontaneous melanoma regression: initial role of MHCII CD163 macrophages.解析导致自发性黑色素瘤消退的免疫反应:MHCII CD163 巨噬细胞的初始作用。
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The MeLiM Minipig: An Original Spontaneous Model to Explore Cutaneous Melanoma Genetic Basis.梅利姆小型猪:一种用于探索皮肤黑色素瘤遗传基础的原始自发模型。
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本文引用的文献

1
Identification of differentially expressed genes in spontaneously regressing melanoma using the MeLiM swine model.使用MeLiM猪模型鉴定自发消退性黑色素瘤中差异表达的基因。
Pigment Cell Melanoma Res. 2008 Apr;21(2):147-61. doi: 10.1111/j.1755-148X.2008.00442.x.
2
The involvement of granulocytes in spontaneous regression of Walker 256 carcinoma.粒细胞在Walker 256癌自发消退中的作用。
Cancer Lett. 2008 Feb 18;260(1-2):180-6. doi: 10.1016/j.canlet.2007.10.039.
3
Functional grouping of osteoclast genes revealed through microarray analysis.通过微阵列分析揭示破骨细胞基因的功能分组。
Biochem Biophys Res Commun. 2008 Feb 8;366(2):352-9. doi: 10.1016/j.bbrc.2007.11.106. Epub 2007 Dec 3.
4
Expression profiling of melanoma cell lines: in search of a progression-related molecular signature.黑色素瘤细胞系的表达谱分析:寻找与进展相关的分子特征。
Future Oncol. 2007 Dec;3(6):609-11. doi: 10.2217/14796694.3.6.609.
5
The role of melanin as protector against free radicals in skin and its role as free radical indicator in hair.黑色素在皮肤中作为自由基保护剂的作用及其在头发中作为自由基指示剂的作用。
Spectrochim Acta A Mol Biomol Spectrosc. 2008 May;69(5):1429-35. doi: 10.1016/j.saa.2007.09.030. Epub 2007 Oct 2.
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A novel promoter regulates calcitonin receptor gene expression in human osteoclasts.一种新型启动子调控人破骨细胞中降钙素受体基因的表达。
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7
Mesenchymal stem cells within tumour stroma promote breast cancer metastasis.肿瘤基质中的间充质干细胞促进乳腺癌转移。
Nature. 2007 Oct 4;449(7162):557-63. doi: 10.1038/nature06188.
8
Apoptosis of melanocytes in vitiligo results from antibody penetration.白癜风中黑素细胞的凋亡是由抗体渗透引起的。
J Autoimmun. 2007 Dec;29(4):281-6. doi: 10.1016/j.jaut.2007.07.012. Epub 2007 Sep 20.
9
NFATc1 induces osteoclast fusion via up-regulation of Atp6v0d2 and the dendritic cell-specific transmembrane protein (DC-STAMP).NFATc1通过上调Atp6v0d2和树突状细胞特异性跨膜蛋白(DC-STAMP)诱导破骨细胞融合。
Mol Endocrinol. 2008 Jan;22(1):176-85. doi: 10.1210/me.2007-0237. Epub 2007 Sep 20.
10
[Regression in malignant melanoma. Definition, etiopathogenesis, morphology and differential diagnosis].[恶性黑色素瘤的消退。定义、病因发病机制、形态学及鉴别诊断]
Pathologe. 2007 Nov;28(6):453-63. doi: 10.1007/s00292-007-0937-3.

黑色素瘤猪自发癌症消退的基因表达特征

Gene expression signature for spontaneous cancer regression in melanoma pigs.

作者信息

Rambow Florian, Piton Guillaume, Bouet Stephan, Leplat Jean-Jaques, Baulande Sylvain, Marrau Angelique, Stam Mark, Horak Vratislav, Vincent-Naulleau Silvia

机构信息

INRA, UMR 314, Laboratoire de Radiobiologie et d'Etude du Génome, F-78350 Jouy-en-Josas, France.

出版信息

Neoplasia. 2008 Jul;10(7):714-26, 1 p following 726. doi: 10.1593/neo.08344.

DOI:10.1593/neo.08344
PMID:18592010
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2435007/
Abstract

Incomplete spontaneous regression of melanoma is common. However, complete melanoma regression is still a very rare phenomenon. Because melanoma is the most immunogenic human malignancy, the mechanisms leading to regression, based on accumulative evidence, are the host's immune responses. Unfortunately, therapies aiming to enhance the patient's natural immunity against melanoma have yet to meet their expectations. Reasons for failure include various immune escape mechanisms, induced by the tumor, that subsequently lead to tolerance. Here, we performed time-dependent gene expression profiling to unravel molecular changes involved in the transition of progressive melanoma to complete tumor regression using a porcine model. The melanoblastomabearing Libechov minipigs are highly suitable for this study because these animals exhibit naturally occurring and regressing melanomas. We were able to identify a molecular signature of the melanoma regression process. Genes regulated in this signature were associated with 1) cell cycle, 2) immune response, and 3) melanocyte differentiation. These genes may shed light on molecular mechanisms involved in complete melanoma regression and indicate what improvements are needed for successful antimelanoma therapy.

摘要

黑色素瘤的不完全自发消退很常见。然而,黑色素瘤的完全消退仍然是一种非常罕见的现象。由于黑色素瘤是人类最具免疫原性的恶性肿瘤,基于累积证据,导致消退的机制是宿主的免疫反应。不幸的是,旨在增强患者对黑色素瘤天然免疫力的疗法尚未达到预期效果。失败的原因包括肿瘤诱导的各种免疫逃逸机制,这些机制随后导致耐受性。在此,我们使用猪模型进行了时间依赖性基因表达谱分析,以揭示进展期黑色素瘤向完全肿瘤消退转变过程中涉及的分子变化。携带成黑色素细胞瘤的利贝霍夫小型猪非常适合这项研究,因为这些动物表现出自然发生和消退的黑色素瘤。我们能够识别黑色素瘤消退过程的分子特征。该特征中调控的基因与1)细胞周期、2)免疫反应和3)黑素细胞分化相关。这些基因可能有助于阐明黑色素瘤完全消退所涉及的分子机制,并指出成功的抗黑色素瘤治疗需要哪些改进。