Inverse Impact of Cancer Drugs on Circular and Linear RNAs in Breast Cancer Cell Lines

Author:

Terrazzan Anna12ORCID,Crudele Francesca3ORCID,Corrà Fabio1,Ancona Pietro1ORCID,Palatini Jeffrey4,Bianchi Nicoletta1ORCID,Volinia Stefano125

Affiliation:

1. Department of Translational Medicine, University of Ferrara, 44121 Ferrara, Italy

2. Laboratory for Advanced Therapy Technologies (LTTA), University of Ferrara, 44121 Ferrara, Italy

3. Genetics Unit, Institute for Maternal and Child Health, Scientific Institute for Research, Hospitalization and Healthcare (IRCCS) Burlo Garofolo, 34137 Trieste, Italy

4. Genomics Core Facility, Centre of New Technologies, University of Warsaw, 02-097 Warsaw, Poland

5. Centrum Nauk Biologiczno-Chemicznych (Biological and Chemical Research Centre), University of Warsaw, 02-089 Warsaw, Poland

Abstract

Altered expression of circular RNAs (circRNAs) has previously been investigated in breast cancer. However, little is known about the effects of drugs on their regulation and relationship with the cognate linear transcript (linRNA). We analyzed the dysregulation of both 12 cancer-related circRNAs and their linRNAs in two breast cancer cell lines undergoing various treatments. We selected 14 well-known anticancer agents affecting different cellular pathways and examined their impact. Upon drug exposure circRNA/linRNA expression ratios increased, as a result of the downregulation of linRNA and upregulation of circRNA within the same gene. In this study, we highlighted the relevance of identifying the drug-regulated circ/linRNAs according to their oncogenic or anticancer role. Interestingly, VRK1 and MAN1A2 were increased by several drugs in both cell lines. However, they display opposite effects, circ/linVRK1 favors apoptosis whereas circ/linMAN1A2 stimulates cell migration, and only XL765 did not alter the ratio of other dangerous circ/linRNAs in MCF-7. In MDA-MB-231 cells, AMG511 and GSK1070916 decreased circGFRA1, as a good response to drugs. Furthermore, some circRNAs might be associated with specific mutated pathways, such as the PI3K/AKT in MCF-7 cells with circ/linHIPK3 correlating to cancer progression and drug-resistance, or NHEJ DNA repair pathway in TP-53 mutated MDA-MB-231 cells.

Funder

FAR2021

Publisher

MDPI AG

Subject

Genetics,Molecular Biology,Biochemistry

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