4.6 Article

Identifying autophagy gene-associated module biomarkers through construction and analysis of an autophagy-mediated ceRNA-ceRNA interaction network in colorectal cancer

Journal

INTERNATIONAL JOURNAL OF ONCOLOGY
Volume 53, Issue 3, Pages 1083-1093

Publisher

SPANDIDOS PUBL LTD
DOI: 10.3892/ijo.2018.4443

Keywords

autophagy; competing endogenous RNA; interaction network; colorectal cancer; prognostic biomarkers

Categories

Funding

  1. National Natural Science Foundation of China [31501075, 31301094]
  2. Natural Science Foundation of Heilongjiang Province [B201302]
  3. Education Department Foundation of Heilongjiang Province [12531227]
  4. Health Department Foundation of Heilongjiang Province [2012-798]
  5. Scientific Research Project of Heilongjiang Provincial Education Department [12541565]

Ask authors/readers for more resources

Autophagy is crucial in cellular homeostasis and has been implicated in the development of malignant tumors. However, the regulatory function of autophagy in cancer remains to be fully elucidated. In the present study, the autophagy-mediated competing endogenous RNA (ceRNA)-ceRNA interaction networks in colorectal cancer (CRC) were constructed by integrating systematically expression profiles of long non-coding RNAs and mRNAs. It was found that a large proportion of autophagy genes were inclined to target hub nodes, including a fraction of autophagy genes, by comparing with other genes within ceRNA networks, and showed preferential interaction with themselves. The present study also revealed that autophagy genes may be used as prognostic markers for cancer therapy. A risk score model based on multivariable Cox regression analysis was then used to capture novel biomarkers in connection with lncRNA for the prognosis of CRC. These biomarkers were confirmed in the test dataset and an additional independent dataset. Furthermore, the prognostic value of biomarkers is independent of conventional clinical factors. These results provide improved understanding of autophagy-mediated ceRNA regulatory mechanisms in CRC and provide novel potential molecular therapeutic targets for the diagnosis and treatment of CRC.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available