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本文引用的文献

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Tumor-cell death, autophagy, and immunity.肿瘤细胞死亡、自噬与免疫。
N Engl J Med. 2012 Mar 22;366(12):1156-8. doi: 10.1056/NEJMcibr1114526.
2
p53/HMGB1 complexes regulate autophagy and apoptosis.p53/HMGB1 复合物调节自噬和细胞凋亡。
Cancer Res. 2012 Apr 15;72(8):1996-2005. doi: 10.1158/0008-5472.CAN-11-2291. Epub 2012 Feb 16.
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EMT and dissemination precede pancreatic tumor formation. EMT 和播散先于胰腺肿瘤形成。
Cell. 2012 Jan 20;148(1-2):349-61. doi: 10.1016/j.cell.2011.11.025.
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Defining the critical hurdles in cancer immunotherapy.定义癌症免疫疗法的关键障碍。
J Transl Med. 2011 Dec 14;9:214. doi: 10.1186/1479-5876-9-214.
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The impact of primary melanoma thickness and microscopic tumor burden in sentinel lymph nodes on melanoma patient survival.原发黑色素瘤厚度和前哨淋巴结中微小肿瘤负荷对黑色素瘤患者生存的影响。
Ann Surg Oncol. 2012 Mar;19(3):1034-42. doi: 10.1245/s10434-011-2095-3. Epub 2011 Oct 12.
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Immunoregulatory molecule B7-H1 (CD274) contributes to skin carcinogenesis.免疫调节分子 B7-H1(CD274)有助于皮肤癌发生。
Cancer Res. 2011 Jul 15;71(14):4737-41. doi: 10.1158/0008-5472.CAN-11-0527. Epub 2011 Jul 5.
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B7-H3 contributes to the metastatic capacity of melanoma cells by modulation of known metastasis-associated genes.B7-H3 通过调节已知的转移相关基因促进黑色素瘤细胞的转移能力。
Int J Cancer. 2012 May 15;130(10):2282-90. doi: 10.1002/ijc.26238. Epub 2011 Aug 8.
8
High-mobility group box 1 is essential for mitochondrial quality control.高迁移率族蛋白 B1 对于线粒体质量控制是必需的。
Cell Metab. 2011 Jun 8;13(6):701-11. doi: 10.1016/j.cmet.2011.04.008.
9
Prognostic significance of mitotic rate in localized primary cutaneous melanoma: an analysis of patients in the multi-institutional American Joint Committee on Cancer melanoma staging database.局限性原发性皮肤黑色素瘤有丝分裂率的预后意义:多机构美国癌症联合委员会黑色素瘤分期数据库患者分析。
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10
Impact of nodal status and tumor burden in sentinel lymph nodes on the clinical outcomes of cancer patients.前哨淋巴结中淋巴结状态和肿瘤负荷对癌症患者临床结局的影响。
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淋巴管、淋巴结和免疫系统:癌症扩散的障碍和门户。

Lymphatics, lymph nodes and the immune system: barriers and gateways for cancer spread.

机构信息

Hillman Cancer Center Research, Pavilion 5117 Centre Avenue, Room 2.26b, Pittsburgh, PA 15213, USA.

出版信息

Clin Exp Metastasis. 2012 Oct;29(7):729-36. doi: 10.1007/s10585-012-9520-2. Epub 2012 Aug 1.

DOI:10.1007/s10585-012-9520-2
PMID:22851005
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3485421/
Abstract

Metastasis to the regional lymph node is the most important prognostic indicator for the outcomes of patients with sold cancer. In general, it is well recognized that cancer development is genetically determined with progression from the microenvironment of the primary tumor site, oftentimes via the SLN gateway, to the distant sites. In about 20 % of the time, the cancer cells may spread directly through the blood vascular system to the distant sites. Thus, in general, cancer progression is consistent with Hellman's spectrum theory in that development of nodal and systemic metastasis from a localized cancer growth is a progressive process. Cancer proliferation within the tumor microenvironment may give rise to increased tumor heterogeneity, which is further complicated by its continuous change through its evolution within the host in a Darwinian sense. It is crucial to understand the molecular process of lymphangiogenesis and hemangiogenesis in the tumor microenvironment with respect to the initial steps of cancer cells entering into the lymphatic and vascular systems so that rational therapy can be developed to curb the process of specific routes of metastasis. This chapter elucidates the role of lymphatics, nodal metastasis and antitumor immunity. We present novel immune targets in nodal metastases, the importance of the lymph node as a pre-metastatic niche, and immune-related proteins as biomarkers of metastasis.

摘要

转移到区域淋巴结是实体瘤患者预后的最重要的预测指标。一般来说,人们普遍认识到癌症的发展是由遗传决定的,从原发性肿瘤部位的微环境开始,通常通过 SLN 途径,发展到远处部位。大约 20%的情况下,癌细胞可能通过血运系统直接播散到远处部位。因此,一般来说,癌症的进展与 Hellman 的谱理论一致,即从局部肿瘤生长发展为淋巴结和全身转移是一个渐进的过程。肿瘤微环境中的癌细胞增殖可能导致肿瘤异质性增加,而通过在宿主中以达尔文的方式进行进化,肿瘤的不断变化使其进一步复杂化。了解肿瘤微环境中的淋巴管生成和血管生成的分子过程对于癌细胞进入淋巴管和血管系统的初始步骤至关重要,这样才能开发出合理的治疗方法来抑制特定转移途径的过程。本章阐述了淋巴管、淋巴结转移和抗肿瘤免疫的作用。我们提出了淋巴结转移中新型免疫靶点、淋巴结作为前转移生态位的重要性以及免疫相关蛋白作为转移的生物标志物。