Abstract

This study aimed to detect expression level of microRNA-383-5p (miR-383-5p) in colorectal cancer (CRC) patients following chemotherapy and its potential influence on the prognosis in CRC. A total of 150 CRC patients treated in The First Affiliated Hospital of Heilongjiang University of Chinese Medicine from June 2016 to July 2019 were included. All patients were preoperatively treated with neoadjuvant chemotherapy. Serum levels of miR-383-5p in CRC patients before and after neoadjuvant chemotherapy were detected by reverse transcriptase-polymerase chain reaction (RT-PCR). Univariable and multivariate unconditioned Cox hazard analyses were conducted to assess risk factors for prognosis in CRC patients. The prognostic value of miR-383-5p in CRC was examined by depicting Kaplan-Meier curves. Overexpression of miR-383-5p could enhance the sensitivity of neoadjuvant chemotherapy in CRC patients. Its level was closely related to differentiation, TNM staging, lymphatic metastasis and vascular infiltration in CRC. Cox hazard analyses demonstrated that stage III+IV, lymphatic metastasis, vascular invasion and low serum level of miR-383-5p were risk factors for prognosis in CRC patients. High level of miR-383-5p was favorable to the overall survival in CRC. MiR-383-5p is lowly expressed in serum of CRC patients. Upregulation of miR-383-5p is beneficial to the therapeutic efficacy of neoadjuvant chemotherapy and the prognosis in CRC.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.