Unknown

Dataset Information

0

Malignant T cells express lymphotoxin ? and drive endothelial activation in cutaneous T cell lymphoma.


ABSTRACT: Lymphotoxin ? (LT?) plays a key role in the formation of lymphatic vasculature and secondary lymphoid structures. Cutaneous T cell lymphoma (CTCL) is the most common primary lymphoma of the skin and in advanced stages, malignant T cells spreads through the lymphatic to regional lymph nodes to internal organs and blood. Yet, little is known about the mechanism of the CTCL dissemination. Here, we show that CTCL cells express LT? in situ and that LT? expression is driven by aberrantly activated JAK3/STAT5 pathway. Importantly, via TNF receptor 2, LT? functions as an autocrine factor by stimulating expression of IL-6 in the malignant cells. LT? and IL-6, together with VEGF promote angiogenesis by inducing endothelial cell sprouting and tube formation. Thus, we propose that LT? plays a role in malignant angiogenesis and disease progression in CTCL and may serve as a therapeutic target in this disease.

SUBMITTER: Lauenborg B 

PROVIDER: S-EPMC4558148 | biostudies-literature | 2015 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications


Lymphotoxin α (LTα) plays a key role in the formation of lymphatic vasculature and secondary lymphoid structures. Cutaneous T cell lymphoma (CTCL) is the most common primary lymphoma of the skin and in advanced stages, malignant T cells spreads through the lymphatic to regional lymph nodes to internal organs and blood. Yet, little is known about the mechanism of the CTCL dissemination. Here, we show that CTCL cells express LTα in situ and that LTα expression is driven by aberrantly activated JAK  ...[more]

Similar Datasets

| S-EPMC6791457 | biostudies-literature
| S-EPMC7913358 | biostudies-literature
| S-EPMC6485670 | biostudies-literature
| S-EPMC3056643 | biostudies-literature
| S-EPMC8844718 | biostudies-literature
| S-EPMC7828698 | biostudies-literature
| S-EPMC3145455 | biostudies-literature
| S-EPMC8894386 | biostudies-literature
| S-EPMC3688772 | biostudies-literature
| S-EPMC7594390 | biostudies-literature