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Homo sapiens

ABSTRACT: Virus Mimicry in the Tumor Microenvironment Activates RIG-I Through Unshielding of Endogenous RNA in Exosomes [exoRNA-Seq]

PROVIDER: PRJNA359787 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR5139262_1.fastq.gz	Fastqsanger.gz
	SRR5139262_2.fastq.gz	Fastqsanger.gz
	SRR5139263_1.fastq.gz	Fastqsanger.gz
	SRR5139263_2.fastq.gz	Fastqsanger.gz
	SRR5139264_1.fastq.gz	Fastqsanger.gz

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Virus Mimicry in the Tumor Microenvironment Activates RIG-I Through Unshielding of Endogenous RNA in Exosomes

Project description:Virus Mimicry in the Tumor Microenvironment Activates RIG-I Through Unshielding of Endogenous RNA in Exosomes

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Project description:Virus Mimicry in the Tumor Microenvironment Activates RIG-I Through Unshielding of Endogenous RNA in Exosomes [RNA-Seq]

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Virus Mimicry in the Tumor Microenvironment Activates RIG-I Through Unshielding of Endogenous RNA in Exosomes [ppp5end RNA-Seq]

Project description:The goal of this study is to investigate if endogenous RNA in exosomes activates RIG-I through unshielding.

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Virus Mimicry in the Tumor Microenvironment Activates RIG-I Through Unshielding of Endogenous RNA in Exosomes [patients RNA-Seq]

Project description:The goal of this study is to investigate if endogenous RNA in exosomes activates RIG-I through unshielding.

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Virus Mimicry in the Tumor Microenvironment Activates RIG-I Through Unshielding of Endogenous RNA in Exosomes [RNA-Seq]

Project description:The goal of this study is to investigate if endogenous RNA in exosomes activates RIG-I through unshielding.

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Virus Mimicry in the Tumor Microenvironment Activates RIG-I Through Unshielding of Endogenous RNA in Exosomes [exoRNA-Seq]

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Differential expression analysis of RNA-seq data from melanocytes driven by tumor cell-derived exosomes

Project description:Exosomes (40–100 nm) are organelle-like membranous structures shed into interstitial spaces and body fluids under diverse pathophysiologic conditions, including tumor development. The tumor microenvironment is abundant with exosomes secreted by the cancer cells themselves. Studies have shown that tumor-derived exosomes can transport RNA and active molecules to other cells to promote tumor growth. Exosomes are increasingly being recognized as a major contributor in the progression of malignant neoplasms. We have found that normal melanocytes can acquire invasiveness through the internalization of melanoma cell-derived exosomes. However, little is known about how the exosomes modulate the melanocytes in the microenvironment to optimize conditions for tumor progression and metastasis. We hypothesize that melanoma cell-derived exosomes can drive the dysregulation of transcriptomes in normal melanocytes and facilitate melanoma progression. Our objective is to identify differentially expressed genes in melanocytes driven by tumor cell-derived exosomes through RNA sequencing and translate those genes as therapeutic targets for melanoma metastasis.

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