MicroRNAs that regulate PTEN as potential biomarkers in colorectal cancer: a systematic review

• Published in: Journal of cancer research and clinical oncology 2020-04, Vol.146 (4), p.809-820
• Main Authors: Liu, Jianrong, Ke, Fei, Chen, Tingting, Zhou, Qing, Weng, Lingling, Tan, Jiani, Shen, Weixing, Li, Liu, Zhou, Jinyong, Xu, Changliang, Cheng, Haibo, Zhou, Jinrong
• Format: Article
• Language: English
• Subjects: Adenoma; Biomarkers, Tumor - genetics; Biomarkers, Tumor - metabolism; Cancer Research; Colorectal cancer; Colorectal carcinoma; Colorectal Neoplasms - enzymology; Colorectal Neoplasms - genetics; Drug resistance; Hematology; Humans; Internal Medicine; Medicine; Medicine & Public Health; Metastases; Metastasis; MicroRNAs; MicroRNAs - genetics; MicroRNAs - metabolism; miRNA; Mucosa; Neoplasia; Oncology; Phosphatase; Protein-tyrosine-phosphatase; PTEN Phosphohydrolase - genetics; PTEN Phosphohydrolase - metabolism; PTEN protein; Review – Cancer Research; Tensin; Tumorigenesis
• ISSN: 0171-5216; 1432-1335
• DOI: 10.1007/s00432-020-03172-3

Purpose MicroRNAs (miRNAs) participate in a variety of biological processes, including tumorigenesis, progression, invasion, and drug resistance to multiple cancers. Phosphatase and tensin homolog (PTEN) is a cancer suppressor gene that has been certified to be regulated by miRNAs in various tumors, including colorectal cancer (CRC). In this review, we screened articles focusing on low PTEN expression in CRC, observed the expression of related miRNAs, analyzed their correlation and relationship with clinicopathological features, and discussed the possibility of these miRNAs as prognostic molecules. Methods We conducted a systematic search for articles published in the Web of Science, PubMed and EBSCO databases between January 1, 2002, and July 18, 2019. We identified these studies by using combinations of the following index entries and key words: ‘colorectal tumor OR colorectal neoplasm OR colorectal carcinoma OR colorectal cancer OR CRC’, ‘protein tyrosine phosphatase OR PTEN’, and ‘microRNA OR MiRNA OR miRNA OR MicroRNA’. Moreover, we evaluated the underlying association between alterations in PTEN and CRC prognosis. Results PTEN expression was obviously lower in CRC tissues than in normal mucosa. However, PTEN expression did not differ significantly between adenoma and normal tissues. PTEN tends to be negatively associated with tumor size and metastasis. MiR-21, miR-200a, miR-543, miR-32, miR-92a, miR-26a, miR-106a and miR-181a were correlated with the downregulation of PTEN. MiR-26a, miR-106a and miR-181a were obviously higher in CRC tissues than in normal tissues, while PTEN was downregulated in CRC tissues. Additionally, miRNAs were mainly positively correlated with distant metastasis, followed by TNM stage. The relationship between miRNAs and tumor differentiation is controversial. However, there were no significant differences between miRNAs and either sex or age. Conclusions The loss of PTEN may be a diagnostic factor for CRC patients. The above-mentioned miRNAs may function as oncogenes in CRC and represent potential targets for CRC therapy. However, further prospective clinical studies are necessary.