# Data for proteomic analysis of murine cardiomyocytic HL-1 cells treated with siRNA against tissue factor

**Authors:** Maura Brioschi, Sabrina Lento, Simona Barcella, Md. Talat Nasim, Stefania Ghilardi, Silvia Stella Barbieri, Elena Tremoli, Cristina Banfi

PMC · DOI: 10.1016/j.dib.2015.02.005 · Data in Brief · 2015-02-25

## TL;DR

This paper provides proteomic data from heart cells treated with siRNA to study the effects of silencing the tissue factor gene.

## Contribution

The study reveals a new role for tissue factor in regulating splicing machinery in cardiomyocytic cells.

## Key findings

- Proteomic analysis identified proteins affected by tissue factor gene silencing.
- Gene Ontology analysis highlighted changes in splicing machinery-related proteins.

## Abstract

This data article is related to the research article entitled Proteomics of Tissue Factor silencing in cardiomyocytic cells reveals a new role for this coagulation factor in splicing machinery control by Lento et al. [1].

Tissue Factor (TF) is a key player in the coagulation cascade, but it has additional functions ranging from angiogenesis, tumour invasion and, in the heart, the maintenance of the integrity of cardiac cells. This article reports the nano-LC–MSE analysis of the cardiomyocytic HL-1 cell line proteome and describes the results obtained from a Gene Ontology analysis of those proteins affected by TF-gene silencing.

## Full-text entities

- **Genes:** F3 (coagulation factor III, tissue factor) [NCBI Gene 14066] {aka CD142, Cf-3, Cf3, TF}, Itpr3 (inositol 1,4,5-triphosphate receptor 3) [NCBI Gene 16440] {aka IP3R 3, IP3R-3, Ip3r3, Itpr-3, tf}
- **Diseases:** tumour (MESH:D009369)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** HL-1 — Mus musculus (Mouse), Transformed cell line (CVCL_0303)

## Full text

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## References

7 references — full list in the complete paper: https://tomesphere.com/paper/PMC4510070/full.md

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Source: https://tomesphere.com/paper/PMC4510070