2021
DOI: 10.1007/978-3-030-83282-7_7
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Noncoding RNAs in Papillary Thyroid Cancer: Interaction with Cancer-Associated Fibroblasts (CAFs) in the Tumor Microenvironment (TME) and Regulators of Differentiation and Lymph Node Metastasis

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Cited by 4 publications
(3 citation statements)
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“…Interestingly, the authors hypothesized that the expression of MEG3 in CAFs may enhance their capability to remodel the ECM through MMP-2 expression and thus favor the propensity for lymph node metastases. However, the correlation between MEG3 expression and MMP-2 production in CAFs requires necessary further investigation and validation in thyroid cancers [ 68 ].…”
Section: Exploring the Role Of Fibroblasts In Thyroid Cancersmentioning
confidence: 99%
“…Interestingly, the authors hypothesized that the expression of MEG3 in CAFs may enhance their capability to remodel the ECM through MMP-2 expression and thus favor the propensity for lymph node metastases. However, the correlation between MEG3 expression and MMP-2 production in CAFs requires necessary further investigation and validation in thyroid cancers [ 68 ].…”
Section: Exploring the Role Of Fibroblasts In Thyroid Cancersmentioning
confidence: 99%
“… 5 Studies have found that although PTC is often inert, vascular invasion is rare, but the rate of lymph node metastasis is high, and some PTC cases have the risk of progression and/or recurrence. 6 , 7 Regional lymph node metastasis is present in 40–90% of PTC patients upon diagnosis, and 15% of cases with lymph node metastasis exhibit aggressive tumor behavior, which is reflected in regional invasion, distant metastasis, treatment tolerance, and increased mortality. 8 Papillary thyroid microcarcinoma (PTMC) is a PTC with the largest tumor diameter ≤1 cm, and its incidence is about 50% of the total incidence.…”
Section: Introductionmentioning
confidence: 99%
“…The tumor microenvironment (TME) is primarily composed of fibroblasts, endothelial cells, different subsets of infiltrating immune cells (IICs), bone marrow-derived progenitor cells, platelets, and inflammatory cytokines ( 5 ). Previous studies have confirmed that tumor cells or host-derived cells (immune cells and fibroblasts, amongst others) in the TME can release various lymphatic angiogenic factors, such as vascular endothelial growth factor (VEGF)-A, C and D, lymphatic vascular factor angiogenin-2, and hepatocyte growth factor, which can stimulate angiogenesis and lymphangiogenesis ( 6 ).…”
Section: Introductionmentioning
confidence: 99%