Journal
THERANOSTICS
Volume 11, Issue 9, Pages 4298-4315Publisher
IVYSPRING INT PUBL
DOI: 10.7150/thno.51342
Keywords
colorectal cancer; N6-methyladenosine (m6A); METTL3; circ1662; YAP1
Categories
Funding
- National Natural Science Foundation of China [81972663, 81560385, U2004112]
- Excellent Youth Science Project of Henan Natural Science Foundation [212300410074]
- Key Scientific Research Projects of Institutions of Higher Education in Henan Province [19A310024]
- Medical Scientific and Technological Research Project of Henan Province [201702027]
- Youth Innovation Fund Project of The First Affiliated Hospital of Zhengzhou University [YNQN2017035]
- China Postdoctoral Science Foundation [2019T120648, 2017M610462]
- National Natural Science Foundation of Henan Province [182300410342]
- Health Commission Technology Talents Overseas Training Project of Henan Province [2018140]
- key scientific research project of Henan higher education institutions [20A310024]
Ask authors/readers for more resources
A novel circRNA, circ1662, was found to be highly expressed in CRC tissues and correlated with poor prognosis and tumor depth. Functionally, circ1662 promoted CRC cell invasion and migration by controlling EMT and accelerating YAP1 nuclear accumulation to regulate the SMAD3 pathway.METTL3 induced circ1662 expression and played a role in CRC metastasis.
Tumor metastasis is the leading cause of death in patients with colorectal cancer (CRC). Circular RNAs (circRNAs) have been shown to be involved in cancer progression. However, the regulatory mechanisms of circRNAs involved in CRC tumor metastasis are currently unknown. Methods: High-throughput sequencing was performed on 6 pairs of CRC and adjacent normal tissues to identify the expression profiles of mRNA and circRNA. circ1662 was assessed by RNA-ISH and IHC of a tissue chip. The function of circ1662 in CRC was evaluated by knocking down or overexpressing circ1662. MeRIP-qPCR, RIP-qPCR, and RNA pull-down were performed to determine the relationship between METTL3, circ1662, and YAP1. Results: A novel circRNA, circ1662, exhibited significantly higher expression in CRC tissues than paired normal tissues. High circ1662 expression was correlated with poor prognosis and tumor depth in patients with CRC. Functionally, circ1662 promoted CRC cell invasion and migration by controlling EMT in vitro and in vivo. Mechanistically, circ1662 directly bound to YAP1 and accelerated its nuclear accumulation to regulate the SMAD3 pathway. Additionally, circ1662 enhanced CRC invasion and migration depending on YAP1 and SMAD3. Interestingly, METTL3 induced circ1662 expression by binding its flanking sequences and installing m6A modifications. Clinically, circ1662 expression strongly correlated with METTL3 and YAP1 protein expression. Moreover, YAP1 expression was negatively correlated with SMAD3 expression. Conclusions: METTL3-induced circ1662 promoted CRC cell invasion and migration by accelerating YAP1 nuclear transport. This result implies that circ1662 is a new prognostic and therapeutic marker for CRC metastasis.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available