The Impact of miRNA in Colorectal Cancer Progression and Its Liver Metastases.
Ovidiu BalacescuDaniel SurCalin CainapSimona VisanDaniel CruceriuRoberta Manzat-SaplacanMihai-Stefan MuresanLoredana BalacescuCosmin LisencuAlexandru IrimiePublished in: International journal of molecular sciences (2018)
Colorectal cancer (CRC) is one of the most commonly diagnosed malignancies with a high incidence and mortality rate. An essential challenge in colorectal cancer management is to identify new prognostic factors that could better estimate the evolution and treatment responses of this disease. Considering their role in cancer development, progression and metastasis, miRNAs have become an important class of molecules suitable for cancer biomarkers discovery. We performed a systematic search of studies investigating the role of miRNAs in colorectal progression and liver metastasis published until October 2018. In this review, we present up-to-date information regarding the specific microRNAs involved in CRC development, considering their roles in alteration of Wnt/βcatenin, EGFR, TGFβ and TP53 signaling pathways. We also emphasize the role of miRNAs in controlling the epithelial⁻mesenchymal transition of CRC cells, a process responsible for liver metastasis in a circulating tumor cell-dependent manner. Furthermore, we discuss the role of miRNAs transported by CRC-derived exosomes in mediating liver metastases, by preparing the secondary pre-metastatic niche and in inducing liver carcinogenesis in a Dicer-dependent manner.
Keyphrases
- liver metastases
- epithelial mesenchymal transition
- prognostic factors
- papillary thyroid
- small cell lung cancer
- signaling pathway
- transforming growth factor
- circulating tumor
- induced apoptosis
- stem cells
- squamous cell
- cell proliferation
- risk factors
- mesenchymal stem cells
- squamous cell carcinoma
- small molecule
- healthcare
- cardiovascular disease
- systematic review
- childhood cancer
- high throughput
- circulating tumor cells
- randomized controlled trial
- endoplasmic reticulum stress
- cell therapy
- pi k akt