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本文引用的文献

1
Study of TLR3, TLR4 and TLR9 in breast carcinomas and their association with metastasis.TLR3、TLR4 和 TLR9 在乳腺癌中的研究及其与转移的关系。
BMC Cancer. 2010 Dec 3;10:665. doi: 10.1186/1471-2407-10-665.
2
Study of TLR3, TLR4, and TLR9 in prostate carcinomas and their association with biochemical recurrence.TLR3、TLR4 和 TLR9 在前列腺癌中的研究及其与生化复发的关系。
Cancer Immunol Immunother. 2011 Feb;60(2):217-26. doi: 10.1007/s00262-010-0931-0. Epub 2010 Oct 27.
3
Dual function of MyD88 in RAS signaling and inflammation, leading to mouse and human cell transformation.MyD88 在 RAS 信号和炎症中的双重功能,导致小鼠和人类细胞转化。
J Clin Invest. 2010 Oct;120(10):3663-7. doi: 10.1172/jci42771.
4
[Human lung cancer: role of TLR7 and TLR8 in cell survival and chemoresistance].[人类肺癌:Toll样受体7和Toll样受体8在细胞存活及化疗耐药中的作用]
Med Sci (Paris). 2010 Apr;26(4):435-7. doi: 10.1051/medsci/2010264435.
5
Triggering of TLR7 and TLR8 expressed by human lung cancer cells induces cell survival and chemoresistance.人肺癌细胞中 TLR7 和 TLR8 的表达触发可诱导细胞存活和化疗耐药性。
J Clin Invest. 2010 Apr;120(4):1285-97. doi: 10.1172/JCI36551. Epub 2010 Mar 8.
6
Toll-like receptors 3 and 7 agonists enhance tumor cell lysis by human gammadelta T cells.Toll样受体3和7激动剂可增强人γδT细胞对肿瘤细胞的裂解作用。
Cancer Res. 2009 Nov 15;69(22):8710-7. doi: 10.1158/0008-5472.CAN-09-1602. Epub 2009 Nov 3.
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In situ stimulation of CD40 and Toll-like receptor 3 transforms ovarian cancer-infiltrating dendritic cells from immunosuppressive to immunostimulatory cells.原位刺激CD40和Toll样受体3可将浸润卵巢癌的树突状细胞从免疫抑制细胞转变为免疫刺激细胞。
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8
[Proteases in cancer progression].[蛋白酶在癌症进展中的作用]
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9
Toll-like receptors expressed in tumor cells: targets for therapy.肿瘤细胞中表达的Toll样受体:治疗靶点
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10
Overexpression of matrix metalloproteinases and their inhibitors in mononuclear inflammatory cells in breast cancer correlates with metastasis-relapse.基质金属蛋白酶及其抑制剂在乳腺癌单核炎性细胞中的过表达与转移复发相关。
Br J Cancer. 2007 Oct 8;97(7):957-63. doi: 10.1038/sj.bjc.6603963. Epub 2007 Sep 11.

TLR3、TLR4、TLR7 和 TLR9 在食管鳞状细胞癌中的过表达。

Overexpression of TLR3, TLR4, TLR7 and TLR9 in esophageal squamous cell carcinoma.

机构信息

Department of Thoracic Surgery of the First Affiliated Hospital, Medical University of Xinjiang, 830054 Urumqi, Xinjiang, China.

出版信息

World J Gastroenterol. 2011 Aug 28;17(32):3745-51. doi: 10.3748/wjg.v17.i32.3745.

DOI:10.3748/wjg.v17.i32.3745
PMID:21990957
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3181461/
Abstract

AIM

To investigate the expression of Toll-like receptor (TLR) 3, TLR4, TLR7 and TLR9 in esophageal squamous cell carcinoma (ESCC).

METHODS

Reverse transcription-polymerase chain reaction and immunohistochemistry were used to analyze the expression of TLR3, TLR4, TLR7 and TLR9 mRNA and protein in samples from 87 esophageal cancer patients consisting of both tumor and normal tissue.

RESULTS

A significant increase in TLR3, TLR4, TLR7 and TLR9 mRNA levels was detected in ESCC samples. Tumors exhibited high TLR protein expression, (70.1%, 72.4%, 66.7% and 78.2% for TLR3, TLR4, TLR7 and TLR9, respectively, P < 0.05). Nevertheless, a significant percentage of tumors also exhibited TLR4 expression in mononuclear inflammatory cells (48.3%) and TLR9 expression in fibroblast-like cells (60.9%). Tumors with high TLR3 expression in tumor cells or high TLR4 expression in mononuclear inflammatory cells were significantly associated with a higher probability of lymph node metastasis and increased depth of invasion. However, tumors with high TLR9 expression in fibroblast-like cells were associated with low probabilities of invasion and metastasis. There was no significant variation between the expression of TLR3, TLR4, TLR7 and TLR9 among different ethnic groups.

CONCLUSION

TLR3, TLR4, TLR7 and TLR9 expression appears important to the biological pathogenesis of ESCC. TLRs may represent therapeutic targets for ESCC.

摘要

目的

研究 Toll 样受体(TLR)3、TLR4、TLR7 和 TLR9 在食管鳞状细胞癌(ESCC)中的表达。

方法

采用逆转录-聚合酶链反应和免疫组织化学方法分析 87 例食管鳞癌患者肿瘤和正常组织中 TLR3、TLR4、TLR7 和 TLR9 mRNA 和蛋白的表达。

结果

ESCC 组织中 TLR3、TLR4、TLR7 和 TLR9 的 mRNA 水平明显升高。肿瘤组织 TLR 蛋白表达较高(TLR3、TLR4、TLR7 和 TLR9 分别为 70.1%、72.4%、66.7%和 78.2%,P < 0.05)。然而,相当比例的肿瘤组织中单核炎性细胞 TLR4 表达(48.3%)和成纤维细胞样细胞 TLR9 表达(60.9%)也较高。肿瘤细胞 TLR3 表达高或单核炎性细胞 TLR4 表达高与淋巴结转移概率增加和浸润深度增加显著相关。然而,成纤维细胞样细胞中 TLR9 表达高与浸润和转移概率降低相关。不同种族间 TLR3、TLR4、TLR7 和 TLR9 的表达无显著差异。

结论

TLR3、TLR4、TLR7 和 TLR9 的表达对 ESCC 的生物学发病机制很重要。TLRs 可能是 ESCC 的治疗靶点。