4.5 Editorial Material

Circling back to epigenetic regulation in osteosarcoma: Comment on 'Hsa_circ_0088212-mediated miR-520h/APOA1 axis inhibits the osteosarcoma progression' by 'Hao Peng'

Journal

TRANSLATIONAL ONCOLOGY
Volume 15, Issue 1, Pages -

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.tranon.2021.101271

Keywords

-

Categories

Funding

  1. INBRE PROGRAM NIH [P20 GM103408]
  2. National Institute of General Medical Sciences

Ask authors/readers for more resources

This commentary evaluates the study conducted by Peng et al. on the identification and function of the signaling axis circ_0088212/miR_520 h/APOA1 in osteosarcoma. The study demonstrates the anti-tumor functions of APOA1 and provides novel context of correlative gene expression with patient outcome. The authors further speculate the potential reasons for contradicting findings in osteosarcoma studies involving circRNAs. The results of the study give confidence that circ_0088212 is a bona fide tumor suppressor in osteosarcoma.
Osteosarcoma is a genetically complex cancer, thus there are increasing efforts to identify biomarkers and regulators within the epigenome that can better predict patient outcomes and provide new therapeutic targets. In this commentary, we have evaluated the work of Peng and colleagues on the identification and function of the signaling axis circ_0088212/miR_520 h/APOA1 in osteosarcoma. We provide the context of how novel it is to demonstrate the anti-tumor functions of APOA1 and not just correlative gene expression with patient outcome. We further postulate why some studies involving circRNAs in osteosarcoma contradict one another. We conclude that the study performed by Peng and colleagues was performed with enough rigor to give confidence that circ_0088212 is a bona fide tumor suppressor in osteosarcoma.

Authors

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

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available