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Colon cancer cells after escape of late apoptosis [exp_1]

ABSTRACT: Colon cancer cells after escape of late apoptosis [exp_1]

PROVIDER: PRJNA720012 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR14150319.fastq.gz	Fastqsanger.gz
	SRR14150320.fastq.gz	Fastqsanger.gz
	SRR14150321.fastq.gz	Fastqsanger.gz
	SRR14150322.fastq.gz	Fastqsanger.gz
	SRR14150323.fastq.gz	Fastqsanger.gz

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Colon cancer cells after escape of late apoptosis

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Peroxireduxin-4 is over-expressed in colon cancer and its down-regulation leads to apoptosis

Project description:The objective of this study was to gain insights into the biological basis of colon cancer progression by characterizing gene expression differences between normal colon epithelium, corresponding colorectal primary tumors and metastases. We found a close similarity in gene expression patterns between primary tumors and metastases, indicating a correlation between gene expression and morphological characteristics. PRDX4 was identified as highly expressed both in primary colon tumors and metastases, and selected for further characterization. Our study revealed that Prdx4 (PrxIV, AOE372) shows functional similarities to other Prx family members by negatively effecting apoptosis induction in tumor cells. In addition, our studies link Prdx4 with Hif-1M-NM-1, a key regulatory factor of angiogenesis. Targeting Prdx4 may be an attractive approach in cancer therapy, as its inhibition is expected to lead to induction of apoptosis and blockade of Hif-1M-NM-1-mediated tumor angiogenesis. mRNA expression profiling of normal colon epithelium (5), primary colon tumors (12 with 1 replicate) and either lymph node metastases (9 with 2 replicates) or liver metastases (2) and cell lines (4) from twelve colon cancer patients.

2011-06-01 | E-GEOD-26571 | biostudies-arrayexpress

Peroxireduxin-4 is over-expressed in colon cancer and its down-regulation leads to apoptosis

Project description:The objective of this study was to gain insights into the biological basis of colon cancer progression by characterizing gene expression differences between normal colon epithelium, corresponding colorectal primary tumors and metastases. We found a close similarity in gene expression patterns between primary tumors and metastases, indicating a correlation between gene expression and morphological characteristics. PRDX4 was identified as highly expressed both in primary colon tumors and metastases, and selected for further characterization. Our study revealed that Prdx4 (PrxIV, AOE372) shows functional similarities to other Prx family members by negatively effecting apoptosis induction in tumor cells. In addition, our studies link Prdx4 with Hif-1α, a key regulatory factor of angiogenesis. Targeting Prdx4 may be an attractive approach in cancer therapy, as its inhibition is expected to lead to induction of apoptosis and blockade of Hif-1α-mediated tumor angiogenesis.

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