2020
DOI: 10.7150/jca.40055
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DRG Neurons Promote Perineural Invasion of Endometrial Cancer via GluR2

Abstract: Background: Perineural invasion (PNI) is correlated with negative prognosis in multiple cancers, but its role in endometrial cancer (EC) is still largely unknown; thus, targeted treatment for nerve infiltration is lacking as well. Methods: The interaction between nerve and EC cells were investigated by in vitro neural invasion assay and transwell coculture system. Then the nerve-related receptor gene glutamate ionotropic receptor AMPA type subunit 2 (GRIA2) was detected in EC tissues and cells using PCR array,… Show more

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Cited by 12 publications
(9 citation statements)
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References 45 publications
(57 reference statements)
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“…In endometrial cancer (EC), GluR2 (GRIA2) expression was upregulated, and the GluR2 antagonist effectively suppressed the invasion, migration, and proliferation of tumor cells. Both in vitro and invivo, EC cells showed its tropism toward DRG neurons and neuron ber which implied that glutamate receptor signal and neuron-tumor interaction play a signi cant role in EC growth (25). Moreover, in the central nervous system, previous studies demonstrated that the generation of synapse and glutamate receptor signals were linked to the progression of high-grade glioma and breast tumor patients, which corroborates with our results of LGG patients (12,(26)(27)(28).…”
Section: Discussionsupporting
confidence: 91%
“…In endometrial cancer (EC), GluR2 (GRIA2) expression was upregulated, and the GluR2 antagonist effectively suppressed the invasion, migration, and proliferation of tumor cells. Both in vitro and invivo, EC cells showed its tropism toward DRG neurons and neuron ber which implied that glutamate receptor signal and neuron-tumor interaction play a signi cant role in EC growth (25). Moreover, in the central nervous system, previous studies demonstrated that the generation of synapse and glutamate receptor signals were linked to the progression of high-grade glioma and breast tumor patients, which corroborates with our results of LGG patients (12,(26)(27)(28).…”
Section: Discussionsupporting
confidence: 91%
“…In endometrial cancer (EC), GluR2 (GRIA2) expression was upregulated, and the GluR2 antagonist effectively suppressed the invasion, migration, and proliferation of tumor cells. Both in vitro and in vivo, EC cells showed its tropism toward DRG neurons and neuron ber which implied that glutamate receptor signal and neuron-tumor interaction play a signi cant role in EC growth (25). Moreover, in the central nervous system, previous studies demonstrated that the generation of synapse and glutamate receptor signals were linked to the progression of high-grade glioma and breast tumor patients, which corroborates with our results of LGG patients (12,(26)(27)(28).…”
Section: Discussionsupporting
confidence: 90%
“…In endometrial cancer (EC), GluR2 (GRIA2) expression was up-regulated, and the GluR2 antagonist effectively suppressed the invasion, migration and proliferation of tumor cells. Both in vitro and in vivo , EC cells showed its tropism toward DRG neurons and neuron fiber which implied that glutamate receptor signal and neuron–tumor interaction play a significant role in EC growth [ 41 ]. Moreover, in the central nervous system, previous studies demonstrated that the generation of synapse and glutamate receptor signals were linked to the progression of high-grade glioma and breast tumor patients, which corroborates with our results of LGG patients [ 16–18 , 42 ].…”
Section: Discussionmentioning
confidence: 99%