Unknown,Transcriptomics,Genomics,Proteomics

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Effects of miR-126/126* of cytokine/chemokine expression in tumor-derived 4T1 cells


ABSTRACT: In order to test the effects of metastasis suppressive miR-126/126* on primary tumor microenvironment, we designed a real-time PCR-based mouse cytokine/chemokine array containing 95 cytokines/chemokines and their receptors. Considering the possibility that production of cytokines/chemokines may be dependent on the interactions among different cell types within the tumor mass, we inoculated GFP-labeled 4T1 cells with a control vector or 4T1 cells with pri-miR-126 overexpression into the fat pad of BALB/c mice. 10 days later, we harvested the primary tumors, isolated GFP-positive cancer cells, and analyzed the expression levels of different cytokines/chemokines and their receptors in the cancer cells at the mRNA level using the cytokine array. qPCR gene expression profiling. Equal amount total RNA from each cell line was pooled prior to gene expression analysis.

ORGANISM(S): Mus musculus

SUBMITTER: Yun Zhang 

PROVIDER: E-GEOD-42885 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

miR-126 and miR-126* repress recruitment of mesenchymal stem cells and inflammatory monocytes to inhibit breast cancer metastasis.

Zhang Yun Y   Yang Pengyuan P   Sun Tao T   Li Dong D   Xu Xin X   Rui Yaocheng Y   Li Chaoran C   Chong Mengyang M   Ibrahim Toni T   Mercatali Laura L   Amadori Dino D   Lu Xincheng X   Xie Dong D   Li Qi-Jing QJ   Wang Xiao-Fan XF  

Nature cell biology 20130210 3


The tumour stroma is an active participant during cancer progression. Stromal cells promote tumour progression and metastasis through multiple mechanisms including enhancing tumour invasiveness and angiogenesis, and suppressing immune surveillance. We report here that miR-126/miR-126(*), a microRNA pair derived from a single precursor, independently suppress the sequential recruitment of mesenchymal stem cells and inflammatory monocytes into the tumour stroma to inhibit lung metastasis by breast  ...[more]

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