Table 1.

qRT-PCR primers used in this study.

Target Gene	Forward primer (5′-3′)	Reverse primers (5′-3′)
HDAC1	CAGGATCCTTATCGTTGACTGG	CGGTGCCAGGAGAAGTAAAG
MCM2	TGGCCAAGAAGGACAACAA	AGCGATGCTGGCAAAGAT
CD47	CCTCCTACACCATCAGCATAC	GACCATGCACTGGGATACAT
GAPDH*	CACCACACCTTCTACAAC	TCTGGGTCATCTTCTCAC
chi-miR-16a-3p	CGCGCGCGAAATTATCTCCAGTATTA
chi-miR-211	CCTTCCCTTTGTCATCCTTTGCCC
chi-miR-155-3p	CTGGGTCTGGCTCCTACATGTT
U6*	CAAGGATGACACGCAAATTCG
novel_circ_0017223	CACCTGTGCCGAGAGCTGTA	CCTGGGCAGCTGGTTTCTGA
novel_circ_0007701	GAAGAAGCTGCCATGAGAAGAG	TGCTGAAGCTGCCGAATATC
novel_circ_0003459	AGATGCTCGCTGCTGCTCTC	ATGAGACGTACGTGTCCCGG
ENSCHIT00000005943	TCAGTGTGCGGTTGACTTAG	CAACCCTCTGCCTTCTCAAA
LNC_012500	CGTAACGCGAATCGCAAAC	TGAGGATCGGGTTAAGGGT
ENSCHIT00000002081	AGACTGTGTCCAGAGGTAACTA	GCTGTGAAAGATGGTGAGTAAATG

*The GADPH gene was used for mRNA, circRNA and lncRNA normalization, while the U6 gene was used for miRNA’s normalization.