# Exploring genes of rectal cancer for new treatments based on protein interaction network

**Authors:** Wenjing Teng, Chao Zhou, Yan Li

bioRxiv · DOI: 10.1101/037531 · bioRxiv · 2016-01-01

## TL;DR

This study explores rectal cancer genes using a protein interaction network to identify key genes and pathways for potential new treatments.

## Contribution

The paper introduces a novel protein-protein interaction network and identifies significant genes for rectal cancer.

## Key findings

- 127 rectal cancer genes were identified as differentially expressed.
- Seven molecular complexes were detected in the PPI network with scores above 7.0.
- Key genes like DDK1 and sparcl1 were found to be significant in the network.

## Abstract

To develop a protein-protein interaction network of rectal cancer, which is based on genetic genes as well as to predict biological pathways underlying the molecular complexes in the network. In order to analyze and summarize genetic markers related to diagnosis and prognosis of rectal cancer.

the genes expression profile was downloaded from OMIM (Online Mendelian Inheritance in Man) database; the protein-protein interaction network of rectal cancer was established by Cytoscape; the molecular complexes in the network were detected by Clusterviz plugin and the pathways enrichment of molecular complexes were performed by DAVID online and Bingo (The Biological Networks Gene Ontology tool).

A total of 127 rectal cancer genes were identified to differentially express in OMIM Database. The protein-protein interaction network of rectal cancer was contained 966 nodes (proteins), 3377 edges (interactive relationships) and 7 molecular complexes (score>7.0). Regulatory effects of genes and proteins were focused on cell cycle, transcription regulation and cellular protein metabolic process. Genes of DDK1, sparcl1, wisp2, cux1, pabpc1, ptk2 and htral were significant nodes in PPI network. The discovery of featured genes which were probably related to rectal cancer, has a great significance on studying mechanism, distinguishing normal and cancer tissues, and exploring new treatments for rectal cancer.

## Linked entities

- **Genes:** MGME1 (mitochondrial genome maintenance exonuclease 1) [NCBI Gene 92667], SPARCL1 (SPARC like 1) [NCBI Gene 8404], CCN5 (cellular communication network factor 5) [NCBI Gene 8839], CUX1 (cut like homeobox 1) [NCBI Gene 1523], PABPC1 (poly(A) binding protein cytoplasmic 1) [NCBI Gene 26986], PTK2 (protein tyrosine kinase 2) [NCBI Gene 5747]
- **Diseases:** rectal cancer (MONDO:0006519)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/10.1101/037531/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/10.1101/037531/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/10.1101/037531/full.md

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Source: https://tomesphere.com/paper/10.1101/037531