A TALEN-based specific transcript knock-down of PIWIL2 suppresses cell growth in HepG2 tumor cell

作者：Chen, Y.; Hu, W.; Lu, Y.; Jiang, S.; Li, C.; Chen, J.; Tao, D.; Liu, Y.; Yang, Y.; Ma, Y.^*

来源：Cell Proliferation, 2014, 47(5): 448-456.

DOI：10.1111/cpr.12120

• TGF-BETA
• ARGONAUTE FAMILY
• C-MYC
• GENE
• MAINTENANCE
• ACTIVATION
• MECHANISMS
• CANCER
• PIRNA
• ZILI

ObjectivesPIWIL2 is widely expressed in various tumours and implicated in playing a role in tumourigenesis. For a more thorough study of PIWIL2 functions in tumour cells, we aimed to establish PIWIL2-specific transcript knock-down/knockout HepG2 cell lines using transcription activator-like effector nuclease (TALEN) technology. Furthermore, we proposed to use the cell models to explore PIWIL2 functions in TGF- signalling in HepG2 cells. HepG2s are human hepatocellular carcinoma cells.
Materials and methodsWe established PIWIL2 knock-down or knock-out cell lines in HepG2 using TALEN technology. Next, we sought to use the cell line models to investigate effects of full length PIWIL2-specific transcripts in cell proliferation induced by TGF-.
ResultsFirst, we established PIWIL2-specific transcript mono-allele and bi-allele knockout HepG2 cell lines. By using the cell line models, we found that specific transcript knockdown of full length PIWIL2 can suppress cell proliferation, while ectopic expression of PIWIL2 enhanced proliferation of HepG2 by suppressing the TGF- pathway. Furthermore, we demonstrated that PIWIL2 can interact with HSP90 to prevent formation of HSP90-TR complexes, which promote degradation of TRs.
ConclusionsTaken together, our study revealed critical negative regulation of TGF- signalling by PIWIL2 in HepG2 tumour cells, and provided an effective strategy to study specific gene transcript functions in cells.

• 出版日期2014-10
• 单位四川大学; 生物治疗国家重点实验室