HNF-1a promotes pancreatic cancer growth and apoptosis resistance via its target gene PKLR. (18th February 2020)
- Record Type:
- Journal Article
- Title:
- HNF-1a promotes pancreatic cancer growth and apoptosis resistance via its target gene PKLR. (18th February 2020)
- Main Title:
- HNF-1a promotes pancreatic cancer growth and apoptosis resistance via its target gene PKLR
- Authors:
- Fan, Zhiyao
Fan, Kun
Deng, Shengming
Gong, Yitao
Qian, Yunzhen
Huang, Qiuyi
Yang, Chao
Cheng, He
Jin, Kaizhou
Luo, Guopei
Liu, Chen
Yu, Xianjun - Abstract:
- Abstract: Pancreatic ductal adenocarcinoma is one of the deadliest malignant tumors, and many genes play important roles in its development. The hepatocyte nuclear factor-1a (HNF-1a) gene encodes HNF-1a, which is a transcriptional activator. HNF-1a regulates the tissue-specific expression of multiple genes, especially in pancreatic islet cells and in the liver. However, the role of the HNF-1a gene in the development of pancreatic cancer is still unclear. Here, we used immunohistochemical staining and real-time PCR to analyze HNF-1a expression in pancreatic cancer tissue. Stable cell lines with HNF-1a knockdown or overexpression were established to analyze the role of HNF-1a in pancreatic cancer cell proliferation and apoptosis by colony formation assay and flow cytometry. We also analyzed the L-type pyruvate kinase (PKLR) promoter sequence to identify the regulatory effect of HNF-1a on PKLR transcription and confirmed the HNF-1a binding site in the PKLR promoter via a chromatin immunoprecipitation assay. HNF-1a was found to be overexpressed in pancreatic cancer and promoted proliferation while inhibiting apoptosis in pancreatic cancer cells. PKLR was identified as the downstream target gene of HNF-1a and binding of HNF-1a at two sites in PKLR (−1931/−1926 and −966/−961) regulated PKLR transcription. In conclusion, HNF-1a is overexpressed in pancreatic cancer, and the transcription factor HNF-1a can promote pancreatic cancer growth and apoptosis resistance via its target geneAbstract: Pancreatic ductal adenocarcinoma is one of the deadliest malignant tumors, and many genes play important roles in its development. The hepatocyte nuclear factor-1a (HNF-1a) gene encodes HNF-1a, which is a transcriptional activator. HNF-1a regulates the tissue-specific expression of multiple genes, especially in pancreatic islet cells and in the liver. However, the role of the HNF-1a gene in the development of pancreatic cancer is still unclear. Here, we used immunohistochemical staining and real-time PCR to analyze HNF-1a expression in pancreatic cancer tissue. Stable cell lines with HNF-1a knockdown or overexpression were established to analyze the role of HNF-1a in pancreatic cancer cell proliferation and apoptosis by colony formation assay and flow cytometry. We also analyzed the L-type pyruvate kinase (PKLR) promoter sequence to identify the regulatory effect of HNF-1a on PKLR transcription and confirmed the HNF-1a binding site in the PKLR promoter via a chromatin immunoprecipitation assay. HNF-1a was found to be overexpressed in pancreatic cancer and promoted proliferation while inhibiting apoptosis in pancreatic cancer cells. PKLR was identified as the downstream target gene of HNF-1a and binding of HNF-1a at two sites in PKLR (−1931/−1926 and −966/−961) regulated PKLR transcription. In conclusion, HNF-1a is overexpressed in pancreatic cancer, and the transcription factor HNF-1a can promote pancreatic cancer growth and apoptosis resistance via its target gene PKLR . … (more)
- Is Part Of:
- Acta biochimica et biophysica Sinica. Volume 52:Number 3(2020)
- Journal:
- Acta biochimica et biophysica Sinica
- Issue:
- Volume 52:Number 3(2020)
- Issue Display:
- Volume 52, Issue 3 (2020)
- Year:
- 2020
- Volume:
- 52
- Issue:
- 3
- Issue Sort Value:
- 2020-0052-0003-0000
- Page Start:
- 241
- Page End:
- 250
- Publication Date:
- 2020-02-18
- Subjects:
- HNF-1a -- pancreatic cancer -- PKLR -- apoptosis
Biochemistry -- Periodicals
Biophysics -- Periodicals
572.05 - Journal URLs:
- http://abbs.oxfordjournals.org/?code=abbs&.cgifields=code&homepage.x=80&homepage.y=13 ↗
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http://www.blackwellpublishing.com/journal.asp?ref=1672-9145&site=1 ↗ - DOI:
- 10.1093/abbs/gmz169 ↗
- Languages:
- English
- ISSNs:
- 1672-9145
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- Legaldeposit
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