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High endothelial venules are rare in colorectal cancers but accumulate in extra-tumoral areas with disease progression.

作者信息

Bento Diana Costa, Jones Emma, Junaid Syed, Tull Justyna, Williams Geraint T, Godkin Andrew, Ager Ann, Gallimore Awen

机构信息

Infection and Immunity; School of Medicine; Henry Wellcome Building; Cardiff University ; Cardiff, UK.

Institute of Medical Genetics; University Hospital of Wales ; Cardiff, UK.

出版信息

Oncoimmunology. 2015 Apr 2;4(3):e974374. doi: 10.4161/2162402X.2014.974374. eCollection 2015 Mar.


DOI:10.4161/2162402X.2014.974374
PMID:25949892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4404788/
Abstract

Prolonged patient survival after surgical resection, is associated with a higher cytotoxic and memory T cell density within colorectal cancers (CRC). High endothelial venules (HEVs) are specialized blood vessels present in secondary lymphoid organs (SLO) that allow ingress of naïve and central memory T cells from the blood. It has been proposed that HEVs in tumors might serve as a similar route of entry for lymphocytes into the tumor and result in an improved prognosis. The present study aimed to characterize HEVs and their microenvironment in resected tumors from colorectal cancer patients ( = 62). We observed HEVs in association with lymphoid aggregates in 49 out of 62 patients. However, these HEV lymphoid aggregates were largely at the invasive margin of the tumor and although there was an association with lymphocytes and HEVs at the invasive margin ( = 0.002) there was only a very weak association with tumor infiltrating lymphocytes. Indeed, lymphoid aggregates were associated with more advanced disease (Dukes' stage C) and did not indicate a favorable prognosis.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f63/4404788/81b36a917b23/koni-04-e974374-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f63/4404788/e0902bc3a4fb/koni-04-e974374-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f63/4404788/e0e530b2508a/koni-04-e974374-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f63/4404788/81b36a917b23/koni-04-e974374-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f63/4404788/e0902bc3a4fb/koni-04-e974374-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f63/4404788/e0e530b2508a/koni-04-e974374-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f63/4404788/81b36a917b23/koni-04-e974374-g003.jpg

相似文献

[1]
High endothelial venules are rare in colorectal cancers but accumulate in extra-tumoral areas with disease progression.

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[2]
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[3]
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[4]
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[7]
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[8]
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[9]
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[10]
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[2]
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Am J Clin Exp Immunol. 2024-12-25

[3]
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[4]
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Front Immunol. 2024

[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Occurrence of tertiary lymphoid tissue is associated with T-cell infiltration and predicts better prognosis in early-stage colorectal cancers.

Clin Cancer Res. 2014-2-12

[2]
Colorectal cancer.

Lancet. 2013-11-11

[3]
Characteristics and significance of colorectal cancer associated lymphoid reaction.

Int J Cancer. 2013-10-24

[4]
The density and type of MECA-79-positive high endothelial venules correlate with lymphocytic infiltration and tumour regression in primary cutaneous melanoma.

Histopathology. 2013-9-14

[5]
Highly prevalent colorectal cancer-infiltrating LAP⁺ Foxp3⁻ T cells exhibit more potent immunosuppressive activity than Foxp3⁺ regulatory T cells.

Mucosal Immunol. 2013-9-25

[6]
Follicular dendritic cells, conduits, lymphatic vessels, and high endothelial venules in tertiary lymphoid organs: Parallels with lymph node stroma.

Front Immunol. 2012-11-30

[7]
High endothelial venules (HEVs) in human melanoma lesions: Major gateways for tumor-infiltrating lymphocytes.

Oncoimmunology. 2012-9-1

[8]
T-cell trafficking facilitated by high endothelial venules is required for tumor control after regulatory T-cell depletion.

Cancer Res. 2012-9-7

[9]
Colorectal cancer in inflammatory bowel disease: what is the real magnitude of the risk?

World J Gastroenterol. 2012-8-7

[10]
Suppression of tumour-specific CD4⁺ T cells by regulatory T cells is associated with progression of human colorectal cancer.

Gut. 2012-8

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