Overexpression of PVT1 could lead to tumorigenesis in three ways. Rearrangements of DNA through the fusion of PVT1 and Oncogene tumor suppressor could lead to the dysregulation of oncogene or tumor suppressor genes, eventually leading to tumorigenesis. Next, expression of the PVT1-encoded miRNAs can downregulate tumor suppressor genes, causing tumorigenesis. Finally, increase in the interaction of MYC with PVT1 can lead to tumorigenesis.[8]
Overexpression of PVT1 located at 8q24.21 region of the chromosome is associated with many cancers in human[8] through dysregulation of certain different genes in different cancers. For instance, the overexpression of PVT1 in prostate Cancer downregulates the miR-146a gene that leads to a decrease of miR-146a levels in a cell, through the methylation of CpG island on its promoter region, promoting the suppression of the cancer cell apoptosis.[9] Furthermore, activity of lncPVT1 and its associated microRNAs has been shown to influence chemotherapy resistance in multiple cancers by epigenetic regulation or direct repression of other non-coding transcripts.[10]
^ abCui M, You L, Ren X, Zhao W, Liao Q, Zhao Y (February 2016). "Long non-coding RNA PVT1 and cancer". Biochemical and Biophysical Research Communications. 471 (1): 10–14. doi:10.1016/j.bbrc.2015.12.101. PMID26850852.
Oh JH, Yang JO, Hahn Y, Kim MR, Byun SS, Jeon YJ, Kim JM, Song KS, Noh SM, Kim S, Yoo HS, Kim YS, Kim NS (December 2005). "Transcriptome analysis of human gastric cancer". Mammalian Genome. 16 (12): 942–954. doi:10.1007/s00335-005-0075-2. PMID16341674. S2CID69278.
