PMID- 33080952 OWN - NLM STAT- MEDLINE DCOM- 20210223 LR - 20210223 IS - 1422-0067 (Electronic) IS - 1422-0067 (Linking) VI - 21 IP - 20 DP - 2020 Oct 18 TI - The Wnt Signalling Pathway: A Tailored Target in Cancer. LID - 10.3390/ijms21207697 [doi] LID - 7697 AB - Cancer is one of the greatest public health challenges. According to the World Health Organization (WHO), 9.6 million cancer deaths have been reported in 2018. The most common cancers include lung, breast, colorectal, prostate, skin (non-melanoma) and stomach cancer. The unbalance of physiological signalling pathways due to the acquisition of mutations in tumour cells is considered the most common cancer driver. The Wingless-related integration site (Wnt)/beta-catenin pathway is crucial for tissue development and homeostasis in all animal species and its dysregulation is one of the most relevant events linked to cancer development and dissemination. The canonical and the non-canonical Wnt/beta-catenin pathways are known to control both physiological and pathological processes, including cancer. Herein, the impact of the Wnt/beta-catenin cascade in driving cancers from different origin has been examined. Finally, based on the impact of Extracellular Vesicles (EVs) on tumour growth, invasion and chemoresistance, and their role as tumour diagnostic and prognostic tools, an overview of the current knowledge linking EVs to the Wnt/beta-catenin pathway is also discussed. FAU - Koni, Malvina AU - Koni M AD - Department of Medical Sciences, University of Turin, Corso Dogliotti 14, 10126 Turin, Italy. FAU - Pinnaro, Veronica AU - Pinnaro V AD - Department of Medical Sciences, University of Turin, Corso Dogliotti 14, 10126 Turin, Italy. FAU - Brizzi, Maria Felice AU - Brizzi MF AD - Department of Medical Sciences, University of Turin, Corso Dogliotti 14, 10126 Turin, Italy. LA - eng GR - IG 2015.17630/Associazione Italiana per la Ricerca sul Cancro/ GR - #2019/Ministero dell'Istruzione, Universita e Ricerca (MIUR) ex 60%./ PT - Journal Article PT - Review DEP - 20201018 PL - Switzerland TA - Int J Mol Sci JT - International journal of molecular sciences JID - 101092791 RN - 0 (MicroRNAs) SB - IM MH - Animals MH - Cell Polarity MH - Extracellular Vesicles/metabolism MH - Humans MH - MicroRNAs/genetics/metabolism MH - *Molecular Targeted Therapy MH - Neoplasms/genetics/*metabolism/*therapy MH - *Wnt Signaling Pathway PMC - PMC7589708 OTO - NOTNLM OT - Wnt/beta-catenin dependent pathway OT - Wnt/beta-catenin independent pathway OT - breast cancer OT - colorectal cancer OT - extracellular vesicles OT - ovarian cancer COIS- The authors declare no conflict of interest. EDAT- 2020/10/22 06:00 MHDA- 2021/02/24 06:00 PMCR- 2020/10/01 CRDT- 2020/10/21 01:02 PHST- 2020/09/29 00:00 [received] PHST- 2020/10/15 00:00 [revised] PHST- 2020/10/16 00:00 [accepted] PHST- 2020/10/21 01:02 [entrez] PHST- 2020/10/22 06:00 [pubmed] PHST- 2021/02/24 06:00 [medline] PHST- 2020/10/01 00:00 [pmc-release] AID - ijms21207697 [pii] AID - ijms-21-07697 [pii] AID - 10.3390/ijms21207697 [doi] PST - epublish SO - Int J Mol Sci. 2020 Oct 18;21(20):7697. doi: 10.3390/ijms21207697.